<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" media="screen" href="/~d/styles/rss2full.xsl"?><?xml-stylesheet type="text/css" media="screen" href="http://feeds.rsc.org/~d/styles/itemcontent.css"?><rss xmlns:a10="http://www.w3.org/2005/Atom" xmlns:feedburner="http://rssnamespace.org/feedburner/ext/1.0" version="2.0"><channel><title>RSC - Green Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/GC</link><description>RSC - Green Chem. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Sat, 25 May 2013 02:43:34 Z</lastBuildDate><category>RSC - Green Chem. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Green Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/GC</link></image><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.rsc.org/rss/GC" /><feedburner:info uri="rss/gc" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40493E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40493E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/q1q5lHPYzZE/C3GC40493E</link><title>Mizoroki-Heck reactions catalyzed by palladium dichloro-bis(aminophosphine) complexes under mild reaction conditions. The importance of ligand composition on the catalytic activity</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40493E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1678-1686&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40493E, Paper&lt;/div&gt;&lt;div&gt;Miriam Oberholzer, Christian M. Frech&lt;br/&gt;The ligand composition of aminophosphines was shown to control the ease of (water-induced) nanoparticle formation and, hence, the catalytic activity of palladium-derived Heck catalysts.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/q1q5lHPYzZE" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Miriam Oberholzer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christian M. Frech</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40493E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40495A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40495A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/qXdzlawiy5U/C3GC40495A</link><title>Highly efficient synthesis of cyclic ureas from CO2 and diamines by a pure CeO2 catalyst using a 2-propanol solvent</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40495A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1567-1577&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40495A, Paper&lt;/div&gt;&lt;div&gt;Masazumi Tamura, Kensuke Noro, Masayoshi Honda, Yoshinao Nakagawa, Keiichi Tomishige&lt;br/&gt;Pure cerium oxide (CeO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;) acts as an effective and reusable heterogeneous catalyst for direct synthesis of cyclic ureas from CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; and diamines even at a low CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; pressure of 0.3 MPa.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/qXdzlawiy5U" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Masazumi Tamura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kensuke Noro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Masayoshi Honda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yoshinao Nakagawa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Keiichi Tomishige</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40495A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40374B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40374B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/rp1PFIGVecQ/C3GC40374B</link><title>The role of flow in green chemistry and engineering</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40374B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1456-1472&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40374B, Critical Review&lt;/div&gt;&lt;div&gt;Stephen G. Newman, Klavs F. Jensen&lt;br/&gt;Methods for running reactions continuously offer numerous environmental advantages over batch reactions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/rp1PFIGVecQ" height="1" width="1"/&gt;</description><a10:updated>2013-04-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Stephen G. Newman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Klavs F. Jensen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40374B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40759D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40759D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/BhU_o9VFWFQ/C3GC40759D</link><title>Benzoylation for the recovery of structure directing agent (di-n-propylamine) from the process effluent of aluminophosphate synthesis</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40759D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1526-1529&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40759D, Communication&lt;/div&gt;&lt;div&gt;Nageswara N. Rao, Smita Masid&lt;br/&gt;A simple benzoylation reaction was used for the recovery of two value added products &lt;em&gt;viz.&lt;/em&gt;, DPBA and AlPO&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;, from the mother liquor of a catalyst manufacturing unit.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/BhU_o9VFWFQ" height="1" width="1"/&gt;</description><a10:updated>2013-04-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nageswara N. Rao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Smita Masid</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40759D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40225H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40225H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/uCDQ0uq50SE/C3GC40225H</link><title>Development of GSK's reagent guides - embedding sustainability into reagent selection</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40225H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1542-1549&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40225H, Paper&lt;/div&gt;&lt;div&gt;Joseph P. Adams, Catherine M. Alder, Ian Andrews, Ann M. Bullion, Matthew Campbell-Crawford, Michael G. Darcy, John D. Hayler, Richard K. Henderson, Catriona A. Oare, Israil Pendrak, Aniko M. Redman, Leanna E. Shuster, Helen F. Sneddon, Matthew D. Walker&lt;br/&gt;Reagent guides were developed to reduce the environmental impact of drug discovery and development.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/uCDQ0uq50SE" height="1" width="1"/&gt;</description><a10:updated>2013-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Joseph P. Adams</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Catherine M. Alder</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ian Andrews</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ann M. Bullion</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew Campbell-Crawford</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael G. Darcy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">John D. Hayler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Richard K. Henderson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Catriona A. Oare</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Israil Pendrak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aniko M. Redman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Leanna E. Shuster</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helen F. Sneddon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew D. Walker</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40225H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40729B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40729B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/n4IK4ANZ--E/C3GC40729B</link><title>Microwave-assisted synthesis of cyclic carbonates by a formic acid/KI catalytic system</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40729B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1673-1677&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40729B, Paper&lt;/div&gt;&lt;div&gt;Jose Tharun, George Mathai, Amal Cherian Kathalikkattil, Roshith Roshan, Joo-Young Kwak, Dae-Won Park&lt;br/&gt;An environment-friendly synthesis of cyclic carbonates from CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; and epoxides with a HCOOH/KI catalytic system was performed in a microwave reactor.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/n4IK4ANZ--E" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jose Tharun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">George Mathai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Amal Cherian Kathalikkattil</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roshith Roshan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joo-Young Kwak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dae-Won Park</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40729B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40314A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40314A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/R8DcdPBs3cI/C3GC40314A</link><title>Selective oxidation of glycerol to lactic acid under acidic conditions using AuPd/TiO2 catalyst</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40314A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1520-1525&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40314A, Communication&lt;/div&gt;&lt;div&gt;Jilei Xu, Hongye Zhang, Yanfei Zhao, Bo Yu, Sha Chen, Yanbin Li, Leiduan Hao, Zhimin Liu&lt;br/&gt;The production of lactic acid from glycerol under acidic conditions was achieved &lt;em&gt;via&lt;/em&gt; selective oxidation of glycerol catalysed by AuPd/TiO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; combined with AlCl&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/R8DcdPBs3cI" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jilei Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongye Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanfei Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bo Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sha Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanbin Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Leiduan Hao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhimin Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40314A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40358K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40358K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/HDZZOiUhSYA/C3GC40358K</link><title>A straightforward double coupling of furan moieties onto epoxidized triglycerides: synthesis of monomers based on two renewable resources</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40358K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1514-1519&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40358K, Communication&lt;/div&gt;&lt;div&gt;Alessandro Gandini, Talita M. Lacerda, Antonio J. F. Carvalho&lt;br/&gt;The bulk reaction of 2-furfuryl amine with epoxidized linseed oil took place at both its ester moieties (aminolysis) and oxirane groups (ring opening) producing three fatty acid furan amides incorporating further furan heterocycles along their chains.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/HDZZOiUhSYA" height="1" width="1"/&gt;</description><a10:updated>2013-04-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alessandro Gandini</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Talita M. Lacerda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio J. F. Carvalho</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40358K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40106E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40106E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/QAXh0qwqOlY/C3GC40106E</link><title>Synthesis of disulfides by laccase-catalyzed oxidative coupling of heterocyclic thiols</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40106E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1490-1495&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40106E, Communication&lt;/div&gt;&lt;div&gt;Heba T. Abdel-Mohsen, Kavitha Sudheendran, Jurgen Conrad, Uwe Beifuss&lt;br/&gt;Laccase-catalyzed oxidative coupling of heterocyclic thiols to the corresponding disulfides has been developed.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/QAXh0qwqOlY" height="1" width="1"/&gt;</description><a10:updated>2013-04-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Heba T. Abdel-Mohsen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kavitha Sudheendran</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jurgen Conrad</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Uwe Beifuss</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40106E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40531A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40531A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/7ZD4cr9wS2U/C3GC40531A</link><title>Soy-castor oil based polyols prepared using a solvent-free and catalyst-free method and polyurethanes therefrom</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40531A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1477-1484&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40531A, Communication&lt;/div&gt;&lt;div&gt;Chaoqun Zhang, Ying Xia, Ruqi Chen, Seungmoo Huh, Patrick A. Johnston, Michael R. Kessler&lt;br/&gt;Green polyol SCP_0.5, prepared from solvent free/catalyst free method, results in polyurethane with excellent thermal and mechanical properties.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/7ZD4cr9wS2U" height="1" width="1"/&gt;</description><a10:updated>2013-04-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chaoqun Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Xia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruqi Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Seungmoo Huh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrick A. Johnston</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael R. Kessler</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40531A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40161H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40161H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/YLDxR9dWKTc/C3GC40161H</link><title>Mesopore-modified mordenites as catalysts for catalytic pyrolysis of biomass and cracking of vacuum gasoil processes</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40161H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1647-1658&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40161H, Paper&lt;/div&gt;&lt;div&gt;S. Stefanidis, K. Kalogiannis, E. F. Iliopoulou, A. A. Lappas, J. Martinez Triguero, M. T. Navarro, A. Chica, F. Rey&lt;br/&gt;Subsequent desilication-dealumination treatments of mordenite zeolites achieve fine tuning of the porous and acid properties of the derived materials.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/YLDxR9dWKTc" height="1" width="1"/&gt;</description><a10:updated>2013-04-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">S. Stefanidis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">K. Kalogiannis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">E. F. Iliopoulou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. A. Lappas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">J. Martinez Triguero</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M. T. Navarro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. Chica</creator><creator xmlns="http://purl.org/dc/elements/1.1/">F. Rey</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40161H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40573G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40573G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/BiQ79JSXHYE/C3GC40573G</link><title>Reactions of hydrophobic organic nanoparticle mixtures in water: nanoparticle-on-nanoparticle oxidative dye bleaching</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40573G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1590-1599&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40573G, Paper&lt;/div&gt;&lt;div&gt;Marco Giardiello, Tom O. McDonald, Jet-Sing Lee, Aled D. Roberts, Andrew Owen, Steve P. Rannard&lt;br/&gt;Reactions of nanoparticulate hydrophobic compounds have been observed in water that exhibit faster rates and lower activation energies than equivalent homogeneous reactions conducted in solvents.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/BiQ79JSXHYE" height="1" width="1"/&gt;</description><a10:updated>2013-04-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marco Giardiello</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tom O. McDonald</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jet-Sing Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aled D. Roberts</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew Owen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steve P. Rannard</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40573G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37085B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37085B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/qQNEtXCfNg4/C3GC37085B</link><title>Cycloaddition of CO2 to epoxides catalyzed by imidazolium-based polymeric ionic liquids</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37085B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1584-1589&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37085B, Paper&lt;/div&gt;&lt;div&gt;Saeideh Ghazali-Esfahani, Hongbing Song, Emilia Paunescu, Felix D. Bobbink, Huizhen Liu, Zhaofu Fei, Gabor Laurenczy, Mojtaba Bagherzadeh, Ning Yan, Paul J. Dyson&lt;br/&gt;A cross-linked ionic polymer derived from a styrene-functionalized imidazolium ionic liquid displays high efficiency and reusability as a heterogeneous catalyst for the cycloaddition of CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; to epoxides.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/qQNEtXCfNg4" height="1" width="1"/&gt;</description><a10:updated>2013-04-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Saeideh Ghazali-Esfahani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongbing Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emilia Paunescu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Felix D. Bobbink</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huizhen Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhaofu Fei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gabor Laurenczy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mojtaba Bagherzadeh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ning Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul J. Dyson</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37085B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40568K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40568K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/yS6ih5SQ5QQ/C3GC40568K</link><title>Carbon dioxide as a reversible amine-protecting agent in selective Michael additions and acylations</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40568K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1550-1557&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40568K, Paper&lt;/div&gt;&lt;div&gt;Annelies Peeters, Rob Ameloot, Dirk E. De Vos&lt;br/&gt;CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; can be used as an efficient protecting agent for amines in Michael additions and acylations at room temperature and atmospheric pressure by the reversible formation of a carbamic acid.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/yS6ih5SQ5QQ" height="1" width="1"/&gt;</description><a10:updated>2013-04-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Annelies Peeters</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rob Ameloot</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dirk E. De Vos</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40568K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00062A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00062A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/pwef-vEnPY0/C3GC00062A</link><title>Sulfonated surfactants obtained from furfural</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00062A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1558-1566&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00062A, Paper&lt;/div&gt;&lt;div&gt;Abdoulaye Gassama, Cedric Ernenwein, Ali Youssef, Mickael Agach, Emmanuel Riguet, Sinisa Marinkovic, Boris Estrine, Norbert Hoffmann&lt;br/&gt;Furfural obtained from biomass is transformed into efficient and biodegradable surfactants. Photooxygenation is used as a sustainable key step.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/pwef-vEnPY0" height="1" width="1"/&gt;</description><a10:updated>2013-04-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Abdoulaye Gassama</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cedric Ernenwein</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ali Youssef</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mickael Agach</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emmanuel Riguet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sinisa Marinkovic</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Boris Estrine</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Norbert Hoffmann</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00062A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40475G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40475G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/L_mC7jkA3AE/C3GC40475G</link><title>Base initiated depolymerization of polycarbonates to epoxide and carbon dioxide co-monomers: a computational study</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40475G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1578-1583&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40475G, Paper&lt;/div&gt;&lt;div&gt;Donald J. Darensbourg, Andrew D. Yeung, Sheng-Hsuan Wei&lt;br/&gt;The base initiated depolymerization of polycarbonates to epoxides and carbon dioxide was calculated to have modest free energy barriers. We expect this mild degradation route to eventually yield recycled polymers of the highest quality.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/L_mC7jkA3AE" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Donald J. Darensbourg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew D. Yeung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sheng-Hsuan Wei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40475G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00092C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00092C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/_B6_SWGUw9Y/C3GC00092C</link><title>Decomposition of hydrogen sulfide in non-thermal plasma aided by supported CdS and ZnS semiconductors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00092C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1509-1513&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00092C, Communication&lt;/div&gt;&lt;div&gt;Lu Zhao, Yao Wang, Liang Jin, Minglei Qin, Xiang Li, Anjie Wang, Chunshan Song, Yongkang Hu&lt;br/&gt;Plasma, aided by semiconductor catalysts, gives rise to complete decomposition of H&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;S with low energy consumption.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/_B6_SWGUw9Y" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lu Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yao Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liang Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minglei Qin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anjie Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunshan Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongkang Hu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00092C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40408K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40408K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/EHkS0WaTc-s/C3GC40408K</link><title>CeO2 as a versatile and reusable catalyst for transesterification of esters with alcohols under solvent-free conditions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40408K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1641-1646&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40408K, Paper&lt;/div&gt;&lt;div&gt;Masazumi Tamura, S. M. A. Hakim Siddiki, Ken-ichi Shimizu&lt;br/&gt;CeO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; acted as an efficient and reusable heterogeneous catalyst for transesterification of various methyl esters with alcohols under the solvent-free conditions, providing a clean, versatile, and economic synthetic method for esters.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/EHkS0WaTc-s" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Masazumi Tamura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">S. M. A. Hakim Siddiki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ken-ichi Shimizu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40408K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40397A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40397A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/qU3MKIMwNn8/C3GC40397A</link><title>NHC-catalyzed reactions of enals with water as a solvent</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40397A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1505-1508&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40397A, Communication&lt;/div&gt;&lt;div&gt;Wendy Wen Yi Leong, Xingkuan Chen, Yonggui Robin Chi&lt;br/&gt;NHC-catalyzed reactions of enals with several electrophiles using water as the only solvent are disclosed.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/qU3MKIMwNn8" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wendy Wen Yi Leong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xingkuan Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yonggui Robin Chi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40397A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40215K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40215K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/HkBttbxr2xI/C3GC40215K</link><title>Piperazine-functionalized ordered mesoporous polymer as highly active and reusable organocatalyst for water-medium organic synthesis</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40215K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1665-1672&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40215K, Paper&lt;/div&gt;&lt;div&gt;Fang Zhang, Xushi Yang, Lei Jiang, Chao Liang, Ruixing Zhu, Hexing Li&lt;br/&gt;A piperazine-functionalized mesoporous polymer (PP-MP) was developed as a highly active and reusable heterogeneous organocatalyst for water-medium organic reactions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/HkBttbxr2xI" height="1" width="1"/&gt;</description><a10:updated>2013-04-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xushi Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chao Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruixing Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hexing Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40215K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40440D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40440D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/EnfN8MHlBT4/C3GC40440D</link><title>Sustainable routes to polyurethane precursors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40440D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1431-1455&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40440D, Tutorial Review&lt;/div&gt;&lt;div&gt;Oliver Kreye, Hatice Mutlu, Michael A. R. Meier&lt;br/&gt;Sustainable alternatives to polyurethane precursors are discussed, focusing on alternative and environmentally more benign procedures for the synthesis of isocyanates, carbamates, as well as polyurethanes.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/EnfN8MHlBT4" height="1" width="1"/&gt;</description><a10:updated>2013-04-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Oliver Kreye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hatice Mutlu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael A. R. Meier</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40440D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40137E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40137E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/qjbPuBZMQSQ/C3GC40137E</link><title>Iron phthalocyanine as an efficient and versatile catalyst for N-alkylation of heterocyclic amines with alcohols: one-pot synthesis of 2-substituted benzimidazoles, benzothiazoles and benzoxazoles</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40137E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1687-1693&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40137E, Paper&lt;/div&gt;&lt;div&gt;Manju Bala, Praveen Kumar Verma, Upendra Sharma, Neeraj Kumar, Bikram Singh&lt;br/&gt;An efficient and versatile method was developed for &lt;em&gt;N&lt;/em&gt;-alkylation of various amines with alcohols by utilizing abundantly available iron phthalocyanine as catalyst.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/qjbPuBZMQSQ" height="1" width="1"/&gt;</description><a10:updated>2013-04-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Manju Bala</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Praveen Kumar Verma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Upendra Sharma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Neeraj Kumar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bikram Singh</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40137E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40262B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40262B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/yYBZqS8JxMA/C3GC40262B</link><title>Efficient ZnBr2-catalyzed reactions of allylic alcohols with indoles, sulfamides and anilines under high-speed vibration milling conditions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40262B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1659-1664&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40262B, Paper&lt;/div&gt;&lt;div&gt;Guang-Peng Fan, Zi Liu, Guan-Wu Wang&lt;br/&gt;Solvent-free reactions of allylic alcohols with various nucleophiles, including indoles, sulfamides and anilines were efficiently achieved in the presence of 20% ZnBr&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; under high-speed vibration milling conditions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/yYBZqS8JxMA" height="1" width="1"/&gt;</description><a10:updated>2013-04-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guang-Peng Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zi Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guan-Wu Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40262B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36976E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36976E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/8R3_Fiv9dKI/C3GC36976E</link><title>Application of multivariate statistics in assessment of green analytical chemistry parameters of analytical methodologies</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36976E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1615-1623&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36976E, Paper&lt;/div&gt;&lt;div&gt;Marek Tobiszewski, Stefan Tsakovski, Vasil Simeonov, Jacek Namiesnik&lt;br/&gt;The study offers a multivariate statistical analysis of a dataset, including the major metrological, "greenness" and methodological parameters of 43 analytical methodologies applied for aldrin determination (a frequently analyzed organic compound) in water samples.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/8R3_Fiv9dKI" height="1" width="1"/&gt;</description><a10:updated>2013-04-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marek Tobiszewski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan Tsakovski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vasil Simeonov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jacek Namiesnik</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36976E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40454D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40454D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/D0MaV19z_Og/C3GC40454D</link><title>Engaging isatins in solvent-free, sterically congested Passerini reaction</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40454D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1608-1614&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40454D, Paper&lt;/div&gt;&lt;div&gt;Trinadh Kaicharla, Santhivardhana Reddy Yetra, Tony Roy, Akkattu T. Biju&lt;br/&gt;A facile, atom-economic and environmentally-benign protocol for the synthesis of biologically important oxindole derivatives in high yields has been demonstrated by employing isatins as carbonyl compound surrogates in a Passerini reaction carried out under solvent-free conditions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/D0MaV19z_Og" height="1" width="1"/&gt;</description><a10:updated>2013-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Trinadh Kaicharla</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Santhivardhana Reddy Yetra</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tony Roy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Akkattu T. Biju</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40454D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40422F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40422F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/MXAfTnkcfhE/C3GC40422F</link><title>Silver-zeolite catalysed solvent free synthesis of (spiro)ketals</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40422F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1496-1500&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40422F, Communication&lt;/div&gt;&lt;div&gt;Sophie Borghese, Pauline Drouhin, Valerie Beneteau, Benoit Louis, Patrick Pale&lt;br/&gt;Ag-doped zeolites acted as highly efficient and recyclable catalysts for the cycloisomerisation of alkyn(edi)ols or acid to (spiro)ketals without solvents and at low Ag loading.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/MXAfTnkcfhE" height="1" width="1"/&gt;</description><a10:updated>2013-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sophie Borghese</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pauline Drouhin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Valerie Beneteau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Benoit Louis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrick Pale</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40422F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37141G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37141G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Q_14UUL-BTs/C3GC37141G</link><title>Tailoring nanohybrids and nanocomposites for catalytic applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37141G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1398-1430&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37141G, Tutorial Review&lt;/div&gt;&lt;div&gt;Filip de Clippel, Michiel Dusselier, Stijn Van de Vyver, Li Peng, Pierre A. Jacobs, Bert F. Sels&lt;br/&gt;Ordered porous inorganic-organic nanocomposites and nanohybrids enable the acquirement of tailor-made properties resulting in highly performing catalysts for applications in fine chemistry and biomass conversion.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/Q_14UUL-BTs" height="1" width="1"/&gt;</description><a10:updated>2013-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Filip de Clippel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michiel Dusselier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stijn Van de Vyver</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Li Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pierre A. Jacobs</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bert F. Sels</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37141G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40407B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40407B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/vmIeHRbraAE/C3GC40407B</link><title>Multistep synthesis of amides from alcohols and amines in continuous flow microreactor systems using oxygen and urea hydrogen peroxide as oxidants</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40407B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1538-1541&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40407B, Paper&lt;/div&gt;&lt;div&gt;Xiaoying Liu, Klavs F. Jensen&lt;br/&gt;Heterogeneous oxidation, gas-liquid separation, and oxidative amidation are integrated to produce amides using alcohols and amines as starting materials.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/vmIeHRbraAE" height="1" width="1"/&gt;</description><a10:updated>2013-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoying Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Klavs F. Jensen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40407B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00024A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00024A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/oAlPNmpVwRc/C3GC00024A</link><title>Sustainable catalysts for methanol carbonylation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00024A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1600-1607&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00024A, Paper&lt;/div&gt;&lt;div&gt;Fengbo Li, Bingfeng Chen, Zhijun Huang, Tao Lu, Yin Yuan, Guoqing Yuan&lt;br/&gt;Well-designed cross-linked copolymers were prepared and used as support for the simultaneous immobilization of rhodium and iodide species.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/oAlPNmpVwRc" height="1" width="1"/&gt;</description><a10:updated>2013-03-27T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fengbo Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bingfeng Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhijun Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yin Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guoqing Yuan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00024A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40104A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40104A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/9ZX_1JHNFNw/C3GC40104A</link><title>N-terminal PEGylated cellulase: a high stability enzyme in 1-butyl-3-methylimidazolium chloride</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40104A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1624-1630&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40104A, Paper&lt;/div&gt;&lt;div&gt;Lu Li, Juan Xie, Shitao Yu, Zhongliang Su, Shiwei Liu, Fusheng Liu, Congxia Xie, Baoquan Zhang, Chenggang Zhang&lt;br/&gt;A high stability enzyme in 1-butyl-3-methylimidazolium chloride was obtained by N-terminal PEGylation of cellulase.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/9ZX_1JHNFNw" height="1" width="1"/&gt;</description><a10:updated>2013-03-22T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Juan Xie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shitao Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhongliang Su</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shiwei Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fusheng Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Congxia Xie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baoquan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chenggang Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40104A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40388B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40388B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ajR8pdwobek/C3GC40388B</link><title>Natural resin shellac as a substrate and a dielectric layer for organic field-effect transistors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40388B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1473-1476&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40388B, Communication&lt;/div&gt;&lt;div&gt;Mihai Irimia-Vladu, Eric Daniel Glowacki, Gunther Schwabegger, Lucia Leonat, Hava Zekiye Akpinar, Helmut Sitter, Siegfried Bauer, Niyazi Serdar Sariciftci&lt;br/&gt;Biocompatible and sustainable electronic-grade materials are integral for the development of electronics for biointegration and 'use-and-throw' applications.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/ajR8pdwobek" height="1" width="1"/&gt;</description><a10:updated>2013-03-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mihai Irimia-Vladu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eric Daniel Glowacki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gunther Schwabegger</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lucia Leonat</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hava Zekiye Akpinar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helmut Sitter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Siegfried Bauer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Niyazi Serdar Sariciftci</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40388B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37107G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37107G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/oQ24QCG_A0o/C3GC37107G</link><title>Iron nanoparticles in situ encapsulated in biochar-based carbon as an effective catalyst for the conversion of biomass-derived syngas to liquid hydrocarbons</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37107G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1631-1640&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37107G, Paper&lt;/div&gt;&lt;div&gt;Qiangu Yan, Caixia Wan, Jian Liu, Jinsen Gao, Fei Yu, Jilei Zhang, Zhiyong Cai&lt;br/&gt;The Fe-core/C-shell nanocomposite catalyst was synthesized by self-assembly at high temperature using char. The catalyst proves highly active and stable for upgrading biosyngas to liquid hydrocarbons.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/oQ24QCG_A0o" height="1" width="1"/&gt;</description><a10:updated>2013-03-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Qiangu Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Caixia Wan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinsen Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fei Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jilei Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiyong Cai</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37107G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40279G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40279G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/To-EGfD10jk/C3GC40279G</link><title>Selective oxidation of dimethyl ether to methyl formate over trifunctional MoO3-SnO2 catalyst under mild conditions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40279G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1501-1504&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40279G, Communication&lt;/div&gt;&lt;div&gt;Guangbo Liu, Qingde Zhang, Yizhuo Han, Noritatsu Tsubaki, Yisheng Tan&lt;br/&gt;Over the MoO&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;-SnO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;(SnCl&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;) catalyst, methyl formate selectivity reached 94.1% at 433 K without the formation of CO&lt;small&gt;&lt;sub&gt;&lt;em&gt;x&lt;/em&gt;&lt;/sub&gt;&lt;/small&gt; from DME oxidation.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/To-EGfD10jk" height="1" width="1"/&gt;</description><a10:updated>2013-03-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guangbo Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qingde Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yizhuo Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Noritatsu Tsubaki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yisheng Tan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40279G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40307F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40307F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/1BLQZSxkY3s/C3GC40307F</link><title>Nanocatalysis in continuous flow: supported iron oxide nanoparticles for the heterogeneous aerobic oxidation of benzyl alcohol</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40307F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1530-1537&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40307F, Paper&lt;/div&gt;&lt;div&gt;David Obermayer, Alina M. Balu, Antonio A. Romero, Walter Goessler, Rafael Luque, C. Oliver Kappe&lt;br/&gt;Investigations on heterogeneous iron catalysis in the selective aerobic oxidation of a primary alcohol are presented.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/1BLQZSxkY3s" height="1" width="1"/&gt;</description><a10:updated>2013-03-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">David Obermayer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alina M. Balu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio A. Romero</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Walter Goessler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rafael Luque</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C. Oliver Kappe</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40307F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00091E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00091E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/3uh4mWw6jUI/C3GC00091E</link><title>Efficient synthesis of quinazoline-2,4(1H,3H)-diones from CO2 and 2-aminobenzonitriles in water without any catalyst</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00091E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1485-1489&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00091E, Communication&lt;/div&gt;&lt;div&gt;Jun Ma, Buxing Han, Jinliang Song, Jiayin Hu, Wenjing Lu, Dezhong Yang, Zhaofu Zhang, Tao Jiang, Minqiang Hou&lt;br/&gt;In the absence of a catalyst, CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; can react with 2-aminobenzonitriles to yield quinazoline- 2,4(1&lt;em&gt;H&lt;/em&gt;,3&lt;em&gt;H&lt;/em&gt;)-diones in water, while the reaction did not take place in organic solvents under the same conditions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/3uh4mWw6jUI" height="1" width="1"/&gt;</description><a10:updated>2013-03-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Buxing Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinliang Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiayin Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenjing Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dezhong Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhaofu Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minqiang Hou</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00091E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40166A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40166A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/5ZhOoPi9iLY/C3GC40166A</link><title>Laser-driven heterogeneous catalysis at room temperature: efficient amide formation catalysed by Au/SiO2 systems</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40166A, Communication&lt;/div&gt;&lt;div&gt;Antonio Pineda, Leyre Gomez, Alina M Balu, Victor Sebastian, Manuel Ojeda, Manuel Arruebo, Antonio Angel Romero Reyes, Jesus Santamaria, Rafael Luque&lt;br/&gt;A proof of concept of laser-assisted heterogeneously catalysed processes at room temperature using silica supported gold nanoparticles is reported. Au/SiO2 nanoparticles were laser-irradiated at 532 nm (SPR maximum absorbance) to...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/5ZhOoPi9iLY" height="1" width="1"/&gt;</description><a10:updated>2013-05-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Pineda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Leyre Gomez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alina M Balu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Victor Sebastian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manuel Ojeda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manuel Arruebo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Angel Romero Reyes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jesus Santamaria</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rafael Luque</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40166A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40267C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40267C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/S9YUVYwlA50/C3GC40267C</link><title>Metal-containing zeolites as efficient catalysts for the transformation of highly valuable chiral biomass-derived products</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40267C, Paper&lt;/div&gt;&lt;div&gt;Avelino Corma, Cecilia Paris, Manuel Moliner&lt;br/&gt;Metal-containing zeolites, specially Sn-Beta, perform as very efficient heterogeneous catalysts in the selective oxidation of levoglucosenone, which is considered as a platform chemical for the production of high-valuable chemicals, towards...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/S9YUVYwlA50" height="1" width="1"/&gt;</description><a10:updated>2013-05-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Avelino Corma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cecilia Paris</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manuel Moliner</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40267C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40740C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40740C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/o0K3sazGv_8/C3GC40740C</link><title>Ultra-Selective Cycloaddition of Dimethylfuran for Renewable p-Xylene with H-BEA.</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40740C, Communication&lt;/div&gt;&lt;div&gt;Wei Fan, Paul Jakob Dauenhauer, Chun-Chih Chang, Sara K Green, C Luke Williams&lt;br/&gt;p-Xylene, the precursor for PET bottles, was synthesized at 90% yield by [4+2] cycloaddition of biomass-derived ethylene and dimethylfuran followed by subsequent dehydration with Beta zeolite.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/o0K3sazGv_8" height="1" width="1"/&gt;</description><a10:updated>2013-05-21T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul Jakob Dauenhauer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chun-Chih Chang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sara K Green</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C Luke Williams</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40740C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40411K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40411K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/IsRmVQ7jWhA/C3GC40411K</link><title>Selective separation of aliphatic and aromatic amines with CO2 switchable ionic liquids aqueous two-phase systems</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40411K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40411K, Paper&lt;/div&gt;&lt;div&gt;Dazhen Xiong, Zhiyong Li, Huiyong Wang, Jianji Wang&lt;br/&gt;Aliphatic and aromatic amines have been separated and recovered with CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; switchable ILs ATPSs at room temperature and atmospheric pressure.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/IsRmVQ7jWhA" height="1" width="1"/&gt;</description><a10:updated>2013-04-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Dazhen Xiong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiyong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huiyong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianji Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40411K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40720A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40720A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ahoqJCJ76gA/C3GC40720A</link><title>Efficient and recyclable rare earth-based catalysts for Friedel-Crafts acylations under microwave heating: dendrimers show the way</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40720A, Communication&lt;/div&gt;&lt;div&gt;Armelle Ouali, Arnaud D. Perrier, Michel Keller, Anne-Marie Caminade, Jean-Pierre Majoral&lt;br/&gt;The catalytic system involving Sc(OTf)3 and a dendritic terpyridine ligand is able to promote the Friedel-Crafts acylation of a wide range of aromatics under microwaves. The expected products are obtained...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/ahoqJCJ76gA" height="1" width="1"/&gt;</description><a10:updated>2013-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Armelle Ouali</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arnaud D. Perrier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michel Keller</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anne-Marie Caminade</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Pierre Majoral</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40720A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40872H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40872H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/JVeEb2gIMNw/C3GC40872H</link><title>Continuous Flow Macrocyclization at High Concentrations: Synthesis of Macrocyclic Lipids</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40872H, Paper&lt;/div&gt;&lt;div&gt;Shawn Collins, Anne-Catherine Bedard, Sophie Regnier&lt;br/&gt;A phase separation/continuous flow macrocyclization protocol eliminates the need for high-dilution conditions and can be used to prepare gram quantities of biologically relevant macrocyclic lipid structures. The method presents several...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/JVeEb2gIMNw" height="1" width="1"/&gt;</description><a10:updated>2013-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shawn Collins</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anne-Catherine Bedard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sophie Regnier</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40872H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40605A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40605A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/69bKXMHwkZc/C3GC40605A</link><title>Living carbocationic polymerization of a vinyl ether monomer derived from soybean oil, 2-(vinyloxy)ethyl soyate</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40605A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40605A, Communication&lt;/div&gt;&lt;div&gt;Andrey Chernykh, Samim Alam, Anurad Jayasooriya, James Bahr, Bret J. Chisholm&lt;br/&gt;A novel vinyl ether monomer was produced from soybean oil by base-catalyzed transesterification of 2-(vinyloxy)ethanol with soybean oil.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/69bKXMHwkZc" height="1" width="1"/&gt;</description><a10:updated>2013-05-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Andrey Chernykh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samim Alam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anurad Jayasooriya</creator><creator xmlns="http://purl.org/dc/elements/1.1/">James Bahr</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bret J. Chisholm</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40605A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37028C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37028C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ttLnWxQkGeA/C3GC37028C</link><title>Formation of glycerol carbonate from glycerol and urea catalysed by metal monoglycerolates</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37028C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37028C, Paper&lt;/div&gt;&lt;div&gt;Terence W. Turney, Antonio Patti, Will Gates, Uzma Shaheen, Sanjitha Kulasegaram&lt;br/&gt;Efficient conversion of glycerol into glycerol carbonate by urea is catalysed by metal monoglycerolate complexes &lt;em&gt;via&lt;/em&gt; a metal isocyanate complex.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/ttLnWxQkGeA" height="1" width="1"/&gt;</description><a10:updated>2013-05-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Terence W. Turney</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Patti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Will Gates</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Uzma Shaheen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sanjitha Kulasegaram</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37028C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40401C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40401C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/9i1jH1ZIZN0/C3GC40401C</link><title>Copper on chitosan: a recyclable heterogeneous catalyst for azide-alkyne cycloaddition reactions in water</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40401C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40401C, Communication&lt;/div&gt;&lt;div&gt;R. B. Nasir Baig, Rajender S. Varma&lt;br/&gt;Copper sulfate has been immobilized over chitosan by simply stirring an aqueous suspension of chitosan in water with copper sulfate; the ensuing catalyst has been utilized for the azide-alkyne cycloaddition in aqueous media and it can be recycled and reused many times without losing its activity.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/9i1jH1ZIZN0" height="1" width="1"/&gt;</description><a10:updated>2013-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">R. B. Nasir Baig</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rajender S. Varma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40401C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40482J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40482J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/UQ3BVuFN93o/C3GC40482J</link><title>Hydrophosphinylation of unactivated alkenes with secondary phosphine oxides under visible-light photocatalysis</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40482J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40482J, Communication&lt;/div&gt;&lt;div&gt;Woo-Jin Yoo, Shu Kobayashi&lt;br/&gt;An environmentally benign catalyst for hydrophosphinylation was developed under visible light irradiation.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/UQ3BVuFN93o" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Woo-Jin Yoo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shu Kobayashi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40482J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40588E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40588E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Z7ehFx51HeU/C3GC40588E</link><title>Unusual reactions mediated by FMN-dependent ene- and nitro-reductases</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40588E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40588E, Critical Review&lt;/div&gt;&lt;div&gt;Katharina Durchschein, Melanie Hall, Kurt Faber&lt;br/&gt;The broad redox potential of the cofactor flavin in the active site of ene- and nitro-reductases from the Old-Yellow-Enzyme family enables a remarkably wide array of reactions, such as the reduction of alkenes, alkynes, arenes, nitro groups and nitrate esters and redox-neutral C[double bond, length as m-dash]C-bond isomerization.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/Z7ehFx51HeU" height="1" width="1"/&gt;</description><a10:updated>2013-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Katharina Durchschein</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Melanie Hall</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kurt Faber</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40588E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37133F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37133F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/zxU3c_MPOYo/C3GC37133F</link><title>Conversion of furfural into cyclopentanone over Ni-Cu bimetallic catalysts</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37133F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37133F, Paper&lt;/div&gt;&lt;div&gt;Yanliang Yang, Zhongtian Du, Yizheng Huang, Fang Lu, Feng Wang, Jin Gao, Jie Xu&lt;br/&gt;Transformation of biomass-derived furfural into cyclopentanone over Ni-Cu bimetallic catalysts was studied in water under a hydrogen atmosphere.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/zxU3c_MPOYo" height="1" width="1"/&gt;</description><a10:updated>2013-04-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yanliang Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhongtian Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yizheng Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fang Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jie Xu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37133F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40730F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40730F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/8gEDMiuWeoo/C3GC40730F</link><title>Aerobic oxidation of primary aliphatic alcohols over bismuth oxide supported platinum catalysts in water</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40730F, Paper&lt;/div&gt;&lt;div&gt;Tianliang Lu, Zhongtian Du, Junxia liu, Hong Ma, Jie Xu&lt;br/&gt;Catalytic oxidation of non-activated aliphatic alcohols with molecular oxygen is rather challenging, especially in aqueous medium in the absence of additional base. Bismuth is usually used as promoter of platinum-based...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/8gEDMiuWeoo" height="1" width="1"/&gt;</description><a10:updated>2013-05-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tianliang Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhongtian Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junxia liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jie Xu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40730F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00060E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00060E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/J9LVjLxCHYE/C3GC00060E</link><title>Synthesis and utilisation of sugar compounds derived from lignocellulosic biomass</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00060E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00060E, Critical Review&lt;/div&gt;&lt;div&gt;Hirokazu Kobayashi, Atsushi Fukuoka&lt;br/&gt;Sugar compounds are a renewable feedstock derived from lignocellulosic biomass for the production of numerous useful chemicals including plastics, fine chemicals and high-grade fuels.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/J9LVjLxCHYE" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hirokazu Kobayashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Atsushi Fukuoka</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00060E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40441B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40441B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/pNmyPK9DjCI/C3GC40441B</link><title>A new MCM-41 supported HPF6 catalyst for the library synthesis of highly substituted 1,4-dihydropyridines and oxidation to pyridines: report of one-dimensional packing towards LMSOMs and studies on their photophysical properties</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40441B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40441B, Paper&lt;/div&gt;&lt;div&gt;Suman Ray, Mike Brown, Asim Bhaumik, Arghya Dutta, Chhanda Mukhopadhyay&lt;br/&gt;New MCM-41/HPF&lt;small&gt;&lt;sub&gt;6&lt;/sub&gt;&lt;/small&gt; catalyst for library synthesis of 1,4-dihydropyridines and oxidation to pyridines.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/pNmyPK9DjCI" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Suman Ray</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mike Brown</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Asim Bhaumik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arghya Dutta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chhanda Mukhopadhyay</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40441B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37129H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37129H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/zlDyK6NoQcY/C3GC37129H</link><title>Methods for the regeneration of nicotinamide coenzymes</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37129H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37129H, Critical Review&lt;/div&gt;&lt;div&gt;Hong Wu, Chunyong Tian, Xiaokai Song, Chuang Liu, Dong Yang, Zhongyi Jiang&lt;br/&gt;This article presents an overview of four kinds of methods used for the regeneration of nicotinamide coenzymes, spanning enzymatic methods, chemical methods, electrochemical methods and photochemical methods.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/zlDyK6NoQcY" height="1" width="1"/&gt;</description><a10:updated>2013-04-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunyong Tian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaokai Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chuang Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dong Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhongyi Jiang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37129H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37054B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37054B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/k57uSJ6DbPI/C3GC37054B</link><title>Aza-Michael versus aminolysis reactions of glycerol carbonate acrylate</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37054B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37054B, Paper&lt;/div&gt;&lt;div&gt;Nohra Bassam, Candy Laure, Blanco Jean-Francois, Raoul Yann, Mouloungui Zephirin&lt;br/&gt;New five-membered cyclic glycerylic carbonate and hydroxyurethane isomers were synthesised from glycerol carbonate, with neither catalysts nor solvents. Experimental parameter effects are reported for the competition between aza-Michael addition and aminolysis reactions.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/k57uSJ6DbPI" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nohra Bassam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Candy Laure</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Blanco Jean-Francois</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Raoul Yann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mouloungui Zephirin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37054B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40421H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40421H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/WDGVqgcaMyA/C3GC40421H</link><title>A highly stable and active magnetically separable Pd nanocatalyst in aqueous phase heterogeneously catalyzed couplings</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40421H, Paper&lt;/div&gt;&lt;div&gt;Mohammad Ali Zolfigol, Vahid Khakyzadeh, Ahmad Reza Moosavi-Zare, Abed Rostami, Abdolkarim Zare, Nasser Iranpoor, Mohammad Hassan Beyzavi, Rafael Luque&lt;br/&gt;An active and stable magnetically separable Pd nanocatalyst was prepared and characterized. The nanocatalyst exhibited excellent activities and reusabilities in aqueous phase processes including the O-arylation of phenols and Sonogashira...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/WDGVqgcaMyA" height="1" width="1"/&gt;</description><a10:updated>2013-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mohammad Ali Zolfigol</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vahid Khakyzadeh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ahmad Reza Moosavi-Zare</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abed Rostami</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abdolkarim Zare</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nasser Iranpoor</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mohammad Hassan Beyzavi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rafael Luque</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40421H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40625C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40625C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/lgjslf_GB14/C3GC40625C</link><title>New Biotechnology Paradigm: Cell-Free Biosystems for Biomanufacturing</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40625C, Perspective&lt;/div&gt;&lt;div&gt;Joe Rollin, Ward Tam, Y-H Percival Zhang&lt;br/&gt;Cost-efficient production of sustainably-derived biochemicals and biofuels is a critical goal of modern biotechnology. The current predominant biotransformation method is mainly based on microbial fermentation, but this system suffers from...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/lgjslf_GB14" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Joe Rollin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ward Tam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Y-H Percival Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40625C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40515J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40515J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/DGL16gooM7c/C3GC40515J</link><title>Synthesis of phenacyl bromides via K2S2O8-mediated tandem hydroxybromination and oxidation of styrenes in water</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40515J, Paper&lt;/div&gt;&lt;div&gt;Qing Jiang, Wenbing Sheng, Cancheng Guo&lt;br/&gt;Nontransition metal-catalyzed synthesis of phenacyl bromides was achieved through K2S2O8-mediated tandem hydroxybromination and oxidation of styrenes. The advantages of this reaction are its excellent functional group compatibility, mild reaction conditions...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/DGL16gooM7c" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Qing Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenbing Sheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cancheng Guo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40515J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40558C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40558C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/sSpuhyZqjew/C3GC40558C</link><title>Catalytic Deoxygenation of Microalgae Oil to Green Hydrocarbons</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40558C, Critical Review&lt;/div&gt;&lt;div&gt;Johannes A Lercher, Chen Zhao, Tomas Brueck&lt;br/&gt;Microalgae are high potential raw biomass material for triglyceride feedstock, due to their high oil content and rapid growth rate, and because algae cultivation does not compete with edible food...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/sSpuhyZqjew" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Johannes A Lercher</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chen Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomas Brueck</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40558C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40437D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40437D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ZmPvYNi3KU0/C3GC40437D</link><title>Enhanced Extraction of Caffeine from Guarana Seeds using Aqueous Solutions of Ionic Liquids</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40437D, Paper&lt;/div&gt;&lt;div&gt;Ana Filipa Claudio, Ana Maria Conceicao Ferreira, Mara G Freire, Joao A.P. Coutinho&lt;br/&gt;The extraction of caffeine from bioresources using more benign and cost-effective processes is of fundamental relevance towards the finding of alternative (bio)pesticides. Classically, the best attempts to extract caffeine from...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/ZmPvYNi3KU0" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ana Filipa Claudio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ana Maria Conceicao Ferreira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mara G Freire</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joao A.P. Coutinho</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40437D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40433A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40433A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/LV8xyLmUouc/C3GC40433A</link><title>Cellulose-derived superparamagnetic carbonaceous solid acid catalyst for cellulose hydrolysis in ionic liquid or aqueous reaction system</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40433A, Paper&lt;/div&gt;&lt;div&gt;Haixin Guo, Youfen Lian, Lulu Yan, Xinhua Qi, Richard L. Smith&lt;br/&gt;A cellulose-derived carbonaceous solid acid catalyst that has superparamagnetism was synthesized by incomplete hydrothermal carbonization of cellulose followed by Fe3O4 grafting and -SO3H groups functionalization. The as-prepared superparamagnetic carbon catalyst...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/LV8xyLmUouc" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haixin Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Youfen Lian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lulu Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinhua Qi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Richard L. Smith</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40433A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40346G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40346G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/2wZ_-k3refg/C3GC40346G</link><title>Environmentally friendly reduction of platinum catalyst precursor supported on polypyrrole</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40346G, Paper&lt;/div&gt;&lt;div&gt;A Sepulveda-Escribano, Robison Buitrago-Sierra, M.Mercedes Pastor-Blas, M. Jesus Garcia-Fernandez&lt;br/&gt;Supported metals are traditionally prepared by impregnating a support material with the metal precursor solution, followed by reduction in hydrogen at elevated temperatures. In this study, a polymeric support has...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/2wZ_-k3refg" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">A Sepulveda-Escribano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robison Buitrago-Sierra</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M.Mercedes Pastor-Blas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M. Jesus Garcia-Fernandez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40346G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40547H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40547H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ZeMtFC3Boes/C3GC40547H</link><title>Flowerlike Mesoporous Silica: A Bifunctionalized Catalyst for Rhodium-Catalyzed Asymmetric Transfer Hydrogenation of Aromatic Ketones in Aqueous Medium</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40547H, Paper&lt;/div&gt;&lt;div&gt;Guohua Liu, Ronghua Jin, Dacheng Zhang, Quanxi Liang, Qunqun Ye&lt;br/&gt;A functionalized flowerlike mesoporous silica with chiral organorhodium functionality incorporated within its silica framework is prepared through an assembly of chiral 4-(trimethoxysilyl)ethyl)phenylsulfonyl-1,2-diphenylethylenediamine and tetraethoxysilane under a cooperative dual-template approach followed...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/ZeMtFC3Boes" height="1" width="1"/&gt;</description><a10:updated>2013-05-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guohua Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ronghua Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dacheng Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Quanxi Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qunqun Ye</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40547H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40360B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40360B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/JMNmoeHJ_KU/C3GC40360B</link><title>Rhodium-catalyzed hydrogenation of olefins in [gamma]-valerolactone-based ionic liquids</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40360B, Communication&lt;/div&gt;&lt;div&gt;Andrea Stradi, Mark Molnar, Mihaly Ovari, Gabor Dibo, Frank U. Richter, Laszlo T. Mika&lt;br/&gt;[gamma]-Valerolactone-based ionic liquids were successfully used as catalyst phase for [Rh(cod)2][BF4]/RP(C6H4-m-SO3Na)2 (R = Me, Pr, Bu, Cp) catalyzed hydrogenation of different olefins. Compared to broadly used ionic liquids e.g 1-butyl-3-methylimidazolium...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/JMNmoeHJ_KU" height="1" width="1"/&gt;</description><a10:updated>2013-05-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Andrea Stradi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mark Molnar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mihaly Ovari</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gabor Dibo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frank U. Richter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laszlo T. Mika</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40360B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00090G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00090G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/798vjjMw3QY/C3GC00090G</link><title>The Electrocatalytic Hydrogenation of Furanic Compounds in a Continuous Electrocatalytic Membrane Reactor</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00090G, Paper&lt;/div&gt;&lt;div&gt;Sara K Green, Jechan Lee, Hyung Ju Kim, Geoffrey A Tompsett, Won Bae Kim, George Huber&lt;br/&gt;The electrocatalytic hydrogenation of biomass derived oxygenates in a continuous electrocatalytic membrane reactor presents a promising method of fuel and chemical production that minimizes usage of solvents and has the...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/798vjjMw3QY" height="1" width="1"/&gt;</description><a10:updated>2013-05-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sara K Green</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jechan Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyung Ju Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Geoffrey A Tompsett</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Won Bae Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">George Huber</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00090G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40450A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40450A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/vfegdV9lfvU/C3GC40450A</link><title>Photocatalysis on Supported gold and silver nanoparticles under ul-traviolet and visible light irradiation</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40450A, Tutorial Review&lt;/div&gt;&lt;div&gt;Sarina Sarina, Eric Waclawik, Huaiyong Zhu&lt;br/&gt;Studies of the optical properties and catalytic capabilities of noble metal nanoparticles (NPs), such as gold (Au) and silver (Ag), have formed the basis for a very recent and fast...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/vfegdV9lfvU" height="1" width="1"/&gt;</description><a10:updated>2013-05-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sarina Sarina</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eric Waclawik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huaiyong Zhu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40450A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40457A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40457A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/x5RnobMAopk/C3GC40457A</link><title>Magnetite-supported sulfonic acid: a retrievable nanocatalyst for Ritter reaction and multicomponent reactions</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40457A, Paper&lt;/div&gt;&lt;div&gt;Manoj B Gawande, Anuj Rathi, Isabel Dias Nogueira, Rajender S Varma, Prof. Paula Branco&lt;br/&gt;Magnetite-sulfonic acid (NanocatFe-OSO3H), prepared by wet-impregnation method, serves as a magnetically retrievable sustainable catalyst for the Ritter reaction, among others, and can be used in several reaction cycles without any...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/x5RnobMAopk" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Manoj B Gawande</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anuj Rathi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Isabel Dias Nogueira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rajender S Varma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Prof. Paula Branco</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40457A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40589C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40589C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/vS4ftfzRy5Q/C3GC40589C</link><title>Recovery and Purification of Indium from Waste Sputtering Target by Selective Solvent Extraction of Sn</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40589C, Paper&lt;/div&gt;&lt;div&gt;Hee-Nam Kang, Kwan-Young Kim, Jong-Young Kim&lt;br/&gt;A large volume of indium is being discarded from electronics factories in the forms of waste sputtering targets, polishing slurry, and etching slurry. Of these, waste sputtering target consists mainly...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/vS4ftfzRy5Q" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hee-Nam Kang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kwan-Young Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jong-Young Kim</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40589C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40702K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40702K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/RavBOH0a9tg/C3GC40702K</link><title>Comparative Performance Evaluation and Systematic Screening of Solvents in a Range of Grignard Reactions</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40702K, Paper&lt;/div&gt;&lt;div&gt;Asha Kadam, Mylinh Nguyen, Michael E Kopach, Paul Richardson, Fabrice Gallou, Zhao-Kui Wan, Wei Zhang&lt;br/&gt;The solvent effect on the Grignard reaction of benzyl, aryl and heteroaromatic substrates has been systematically evaluated based on reaction efficiency, ease of subsequent work-up, safety and greenness. 2-Methyltetrahydrofuran (2-MeTHF),...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/RavBOH0a9tg" height="1" width="1"/&gt;</description><a10:updated>2013-05-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Asha Kadam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mylinh Nguyen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael E Kopach</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul Richardson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabrice Gallou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhao-Kui Wan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40702K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40449H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40449H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/nCNi9W-g-IA/C3GC40449H</link><title>Ionic liquids as cosolvents for glycosylation by sucrose phosphorylase: balancing acceptor solubility and enzyme stability.</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40449H, Paper&lt;/div&gt;&lt;div&gt;Karel De Winter, Kristien Verlinden, Vladimir Kren, Lenka Weignerova, Wim Soetaert, Tom Desmet&lt;br/&gt;Over the past decade, disaccharide phosphorylases have received increasing attention as promising biocatalysts for glycoside synthesis. Unfortunately, these enzymes typically have a very low affinity for non-carbohydrate acceptors, which urges...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/nCNi9W-g-IA" height="1" width="1"/&gt;</description><a10:updated>2013-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Karel De Winter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kristien Verlinden</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vladimir Kren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lenka Weignerova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wim Soetaert</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tom Desmet</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40449H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40592C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40592C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/kZIfUoumJnU/C3GC40592C</link><title>Synergistic catalysis by aerogel supported ionic liquid phase (ASILP) in synthesis of 1,5-benzodiazepines</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40592C, Communication&lt;/div&gt;&lt;div&gt;Rajanikant Kurane, Sharanbasappa Khanapure, Jagannath Shrimant Jadhav, Rajashri S Salunkhe, Gajanan Shankarrao Rashinkar&lt;br/&gt;An ionic liquid film of [Bmim]Cl containing organometallic catalyst (Cp2ZrCl2) has been anchored on the porous matrix of aerogel by adsorption interactions. The synthesized aerogel supported ionic liquid phase catalyst...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/kZIfUoumJnU" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Rajanikant Kurane</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sharanbasappa Khanapure</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jagannath Shrimant Jadhav</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rajashri S Salunkhe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gajanan Shankarrao Rashinkar</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40592C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40352A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40352A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Wt0MKlFdWoI/C3GC40352A</link><title>Continuous pretreatment of sugarcane bagasse at high loading in an ionic liquid using a twin-screw extruder</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40352A, Paper&lt;/div&gt;&lt;div&gt;Ayla Sant'Ana da Silva, Ricardo Sposina Sobral Teixeira, Takashi Endo, Elba Pinto da Silva Bon, Seung-Hwan Lee&lt;br/&gt;Ionic liquids (ILs) are innovative and effective solvents for pretreating lignocellulose biomasses because they bring about a noticeable increase in the enzymatic saccharification of these materials. However, the reported solid...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/Wt0MKlFdWoI" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ayla Sant'Ana da Silva</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ricardo Sposina Sobral Teixeira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takashi Endo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elba Pinto da Silva Bon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Seung-Hwan Lee</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40352A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40195B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40195B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Fqh9rXhvQPI/C3GC40195B</link><title>Stereoselective organic reactions promoted by immobilized chiral catalysts in continuous flow systems</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40195B, Tutorial Review&lt;/div&gt;&lt;div&gt;Alessandra Puglisi, Maurizio Benaglia, Valerio Chiroli&lt;br/&gt;The immobilization of the catalyst on a support with the aim of facilitating the separation of the product from the catalyst, and thus the recovery and recycling of the latter,...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/Fqh9rXhvQPI" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alessandra Puglisi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maurizio Benaglia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Valerio Chiroli</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40195B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40668G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40668G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Qb3OeeSKS4s/C3GC40668G</link><title>A General and Practical Oxidation of Alcohols to Primary Amides under Metal-Free Conditions</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40668G, Paper&lt;/div&gt;&lt;div&gt;Xiao-Feng Wu, Muhammad Sharif, Jian-bo Feng, Helfried Neumann, Anahit Pews-Davtyan, Peter Langer, Matthias Beller&lt;br/&gt;A general procedure for oxidation both benzyl alcohols and alkyl alcohols to primary amides under catalyst free conditions has been developed. 34 examples of primary amides were produced from their...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/Qb3OeeSKS4s" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao-Feng Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Muhammad Sharif</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian-bo Feng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helfried Neumann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anahit Pews-Davtyan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter Langer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthias Beller</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40668G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40375K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40375K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/uIQ1pvFKLyo/C3GC40375K</link><title>Magnetically recyclable magnetite-ceria (Nanocat-Fe-Ce) nanocatalyst - applications in multicomponent reactions under benign conditions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40375K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1226-1231&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40375K, Paper&lt;/div&gt;&lt;div&gt;Manoj B. Gawande, Vasco D. B. Bonifacio, Rajender S. Varma, Isabel D. Nogueira, Nenad Bundaleski, C. Amjad A. Ghumman, Orlando M. N. D. Teodoro, Paula S. Branco&lt;br/&gt;Sustainable protocol provides functionalized 1,4-dihydropyrines and tetrahydropyridine using recyclable nano-catalyst.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/uIQ1pvFKLyo" height="1" width="1"/&gt;</description><a10:updated>2013-04-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Manoj B. Gawande</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vasco D. B. Bonifacio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rajender S. Varma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Isabel D. Nogueira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nenad Bundaleski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C. Amjad A. Ghumman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Orlando M. N. D. Teodoro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paula S. Branco</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40375K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40359A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40359A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/9ExS3bwOPq4/C3GC40359A</link><title>Development of a solvent selection guide for aldehyde-based direct reductive amination processes</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40359A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1159-1165&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40359A, Communication&lt;/div&gt;&lt;div&gt;Fiona I. McGonagle, Donna S. MacMillan, Jane Murray, Helen F. Sneddon, Craig Jamieson, Allan J. B. Watson&lt;br/&gt;A solvent selection guide has been developed to facilitate replacement of CH&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;Cl&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;, DCE, and DMF for the direct reductive amination of aldehydes using borane-based reductants.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/9ExS3bwOPq4" height="1" width="1"/&gt;</description><a10:updated>2013-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fiona I. McGonagle</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Donna S. MacMillan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jane Murray</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helen F. Sneddon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Craig Jamieson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Allan J. B. Watson</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40359A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37027E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37027E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/aSpO_za-AeU/C3GC37027E</link><title>Unravelling the structure and function of human hair</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37027E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1268-1273&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37027E, Paper&lt;/div&gt;&lt;div&gt;Ramiz A. Boulos, Ela Eroglu, Xianjue Chen, Adrian Scaffidi, Ben R. Edwards, Jeremiah Toster, Colin L. Raston&lt;br/&gt;The use of an IL composite is successful in unravelling the structure of often-discarded human hair with the components having applications in wastewater treatment and drug coating.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/aSpO_za-AeU" height="1" width="1"/&gt;</description><a10:updated>2013-04-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ramiz A. Boulos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ela Eroglu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xianjue Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Adrian Scaffidi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ben R. Edwards</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jeremiah Toster</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Colin L. Raston</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37027E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36710J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36710J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/0hDVd9Autjg/C3GC36710J</link><title>Substrate dependent synergetic and antagonistic interaction of ammonium halide and polyoxometalate catalysts in the synthesis of cyclic carbonates from oleochemical epoxides and CO2</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36710J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1173-1182&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36710J, Paper&lt;/div&gt;&lt;div&gt;Jens Langanke, Lasse Greiner, Walter Leitner&lt;br/&gt;Oleochemical cyclic carbonates are accessible from the corresponding epoxides and CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; with high &lt;em&gt;cis&lt;/em&gt;-selectivity under synergistic activation by ammonium halides and polyoxometalates (POMs).&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/0hDVd9Autjg" height="1" width="1"/&gt;</description><a10:updated>2013-04-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jens Langanke</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lasse Greiner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Walter Leitner</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36710J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40324F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40324F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Nrs8XAneel0/C3GC40324F</link><title>Alkali silicates and structured mesoporous silicas from biomass power station wastes: the emergence of bio-MCMs</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40324F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1203-1210&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40324F, Paper&lt;/div&gt;&lt;div&gt;J. R. Dodson, E. C. Cooper, A. J. Hunt, A. Matharu, J. Cole, A. Minihan, J. H. Clark, D. J. Macquarrie&lt;br/&gt;High value mesoporous MCM-41 is formed from low value commercial biomass waste ashes.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/Nrs8XAneel0" height="1" width="1"/&gt;</description><a10:updated>2013-04-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">J. R. Dodson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">E. C. Cooper</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. J. Hunt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. Matharu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">J. Cole</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. Minihan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">J. H. Clark</creator><creator xmlns="http://purl.org/dc/elements/1.1/">D. J. Macquarrie</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40324F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40300A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40300A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/3aBFLF4Wh4k/C3GC40300A</link><title>Polyterpenes by ring opening metathesis polymerization of caryophyllene and humulene</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40300A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1112-1115&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40300A, Communication&lt;/div&gt;&lt;div&gt;Etienne Grau, Stefan Mecking&lt;br/&gt;Catalytic polymerization of the common sesquiterpenes caryophyllene and humulene, and post-polymerization modification yield non-crosslinked linear polymers with unique microstructures.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/3aBFLF4Wh4k" height="1" width="1"/&gt;</description><a10:updated>2013-03-28T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Etienne Grau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan Mecking</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40300A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36828A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36828A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/oQCa7UYlQgQ/C3GC36828A</link><title>Control of the selectivity in multi-functional group molecules using supported gold-palladium nanoparticles</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36828A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1244-1254&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36828A, Paper&lt;/div&gt;&lt;div&gt;Hamed Alshammari, Peter J. Miedziak, David J. Morgan, David W. Knight, Graham J. Hutchings&lt;br/&gt;The selectivity during the reaction of substrates with multiple functional groups is manipulated by varying the gold to palladium ratio in a bimetallic catalyst.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/oQCa7UYlQgQ" height="1" width="1"/&gt;</description><a10:updated>2013-03-27T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hamed Alshammari</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter J. Miedziak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David J. Morgan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David W. Knight</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Graham J. Hutchings</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36828A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40297E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40297E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/nmUSCpAGxRI/C3GC40297E</link><title>Mesoporous poly-melamine-formaldehyde (mPMF) - a highly efficient catalyst for chemoselective acetalization of aldehydes</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40297E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1127-1132&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40297E, Communication&lt;/div&gt;&lt;div&gt;Mei Xuan Tan, Liuqun Gu, Nannan Li, Jackie Y. Ying, Yugen Zhang&lt;br/&gt;A mesoporous poly-melamine-formaldehyde (mPMF) polymer was found to be highly effective in catalyzing chemoselective acetalization of aldehydes, without the need for any dehydrating agents.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/nmUSCpAGxRI" height="1" width="1"/&gt;</description><a10:updated>2013-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mei Xuan Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liuqun Gu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nannan Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jackie Y. Ying</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yugen Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40297E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00063J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00063J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/sugtVVoWB2Y/C3GC00063J</link><title>Suzuki-Miyaura cross-coupling reactions using a low-leaching and highly recyclable gold-supported palladium material and two types of microwave equipments</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00063J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1142-1145&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00063J, Communication&lt;/div&gt;&lt;div&gt;Mohammad Al-Amin, Masayoshi Akimoto, Tsuyoshi Tameno, Yuuta Ohki, Naoyuki Takahashi, Naoyuki Hoshiya, Satoshi Shuto, Mitsuhiro Arisawa&lt;br/&gt;Efficient Suzuki-Miyaura cross-coupling reactions with sulfur-modified Au-supported Pd material using single-mode and multi-mode microwaves.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/sugtVVoWB2Y" height="1" width="1"/&gt;</description><a10:updated>2013-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mohammad Al-Amin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Masayoshi Akimoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tsuyoshi Tameno</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuuta Ohki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Naoyuki Takahashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Naoyuki Hoshiya</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Satoshi Shuto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mitsuhiro Arisawa</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00063J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36899H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36899H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/55zPyYweY1c/C3GC36899H</link><title>Directed laccase evolution for improved ionic liquid resistance</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36899H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1348-1355&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36899H, Paper&lt;/div&gt;&lt;div&gt;Haifeng Liu, Leilei Zhu, Marco Bocola, Nora Chen, Antje C. Spiess, Ulrich Schwaneberg&lt;br/&gt;Laccase (lcc2) variants were obtained with improved resistance in the presence of [EMIM] [EtSO&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;] by directed evolution.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/55zPyYweY1c" height="1" width="1"/&gt;</description><a10:updated>2013-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haifeng Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Leilei Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marco Bocola</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nora Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antje C. Spiess</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich Schwaneberg</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36899H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36932C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36932C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/h6U2wTkF9RM/C3GC36932C</link><title>Recycling Pd colloidal catalysts using polymeric phosphine ligands and polyethylene as a solvent</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36932C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1361-1367&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36932C, Paper&lt;/div&gt;&lt;div&gt;Nilusha Priyadarshani, Jakkrit Suriboot, David E. Bergbreiter&lt;br/&gt;Polyisobutylene (PIB)-bound azo dyes were prepared from aryl amine terminated polyisobutylene oligomers and used to form palladacycle precatalysts that can be used for catalytic carbon-carbon cross coupling reactions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/h6U2wTkF9RM" height="1" width="1"/&gt;</description><a10:updated>2013-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nilusha Priyadarshani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jakkrit Suriboot</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David E. Bergbreiter</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36932C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40147B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40147B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/nGIkC-dARrY/C3GC40147B</link><title>Facile insertion of CO2 into metal-phenoxide bonds</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40147B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1356-1360&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40147B, Paper&lt;/div&gt;&lt;div&gt;Sait Elmas, M. Afzal Subhani, Henning Vogt, Walter Leitner, Thomas E. Muller&lt;br/&gt;The insertion of CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; into cobalt- and zinc-phenoxide bonds was found to occur rapidly suggesting it to be a facile key-step in the copolymerisation of carbon dioxide with epoxides.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/nGIkC-dARrY" height="1" width="1"/&gt;</description><a10:updated>2013-03-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sait Elmas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M. Afzal Subhani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Henning Vogt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Walter Leitner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas E. Muller</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40147B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40185E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40185E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/-gAc9kuh64I/C3GC40185E</link><title>Facile conversion of glycosyloxymethyl-furfural into [gamma]-keto-carboxylic acid building blocks towards a sustainable chemical industry</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40185E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1368-1372&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40185E, Paper&lt;/div&gt;&lt;div&gt;Andreas Brust, Frieder W. Lichtenthaler&lt;br/&gt;Sucrose-based glycosyloxymethyl-furfural (GMF) was converted into [gamma]-keto-carboxylic acid building blocks. The conversion into &lt;em&gt;N&lt;/em&gt;-heterocycles is demonstrated using benign chemistry pathways.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/-gAc9kuh64I" height="1" width="1"/&gt;</description><a10:updated>2013-03-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Andreas Brust</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frieder W. Lichtenthaler</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40185E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37086K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37086K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/4QUy-VJg8rY/C3GC37086K</link><title>Acid enhanced ionic liquid pretreatment of biomass</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37086K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1264-1267&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37086K, Paper&lt;/div&gt;&lt;div&gt;Dan Groff, Anthe George, Ning Sun, Noppadon Sathitsuksanoh, Gregory Bokinsky, Blake A. Simmons, Bradley M. Holmes, Jay D. Keasling&lt;br/&gt;Amberlyst 15 enhanced IL pretreatment of switchgrass boosted the yield of sugar up to ten times, decreased the amount of cellulase required for saccharification and increased the biocatalytic conversion of switchgrass into free fatty acids 10-fold to 22% of the theoretical yield.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/4QUy-VJg8rY" height="1" width="1"/&gt;</description><a10:updated>2013-03-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Dan Groff</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anthe George</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ning Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Noppadon Sathitsuksanoh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gregory Bokinsky</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Blake A. Simmons</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bradley M. Holmes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jay D. Keasling</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37086K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37034H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37034H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/1ZMi617dO9A/C3GC37034H</link><title>A silver and water free metathesis reaction: a route to ionic liquids</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37034H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1341-1347&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37034H, Paper&lt;/div&gt;&lt;div&gt;Hassan Srour, Helene Rouault, Catherine C. Santini, Yves Chauvin&lt;br/&gt;A versatile, low-cost, silver and water-free metathesis reaction using melt amine chloride as a solvent yields ionic liquids in high purity ([greater-than-or-equal]99.5%) and high yields ([greater-than-or-equal]90%).&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/1ZMi617dO9A" height="1" width="1"/&gt;</description><a10:updated>2013-03-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hassan Srour</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helene Rouault</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Catherine C. Santini</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yves Chauvin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37034H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40465J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40465J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/WkWMYEPmiqo/C3GC40465J</link><title>Substrate imprinted lipase nanogel for one-step synthesis of chloramphenicol palmitate</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40465J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1155-1158&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40465J, Communication&lt;/div&gt;&lt;div&gt;Rui Wang, Yifei Zhang, Jinhai Huang, Diannan Lu, Jun Ge, Zheng Liu&lt;br/&gt;Lipase nanogel imprinted with its substrate, palmitic acid, during lyophilization has the molecular 'cavities' in polymer shells that enhanced substrate transport and recognition. The imprinting treatment increased the apparent activity in catalyzing the transesterification reaction between chloramphenicol and vinyl palmitate.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/WkWMYEPmiqo" height="1" width="1"/&gt;</description><a10:updated>2013-03-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Rui Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yifei Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinhai Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Diannan Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Ge</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zheng Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40465J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40295A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40295A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/5wk3C7EYTug/C3GC40295A</link><title>Enzymatic cleavage of lignin [small beta]-O-4 aryl ether bonds via net internal hydrogen transfer</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40295A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1373-1381&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40295A, Paper&lt;/div&gt;&lt;div&gt;Jochen Reiter, Harald Strittmatter, Lars O. Wiemann, Doris Schieder, Volker Sieber&lt;br/&gt;A four enzyme system for the reductive cleavage of lignin ether bonds and complete cofactor recycling was established and applied to technical lignin for monomer release.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/5wk3C7EYTug" height="1" width="1"/&gt;</description><a10:updated>2013-03-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jochen Reiter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Harald Strittmatter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lars O. Wiemann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Doris Schieder</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Volker Sieber</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40295A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40319J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40319J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/MFp80tbGkQg/C3GC40319J</link><title>Homogeneous isocyanate- and catalyst-free synthesis of polyurethanes in aqueous media</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40319J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1121-1126&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40319J, Communication&lt;/div&gt;&lt;div&gt;Haritz Sardon, Amanda C. Engler, Julian M. W. Chan, Daniel J. Coady, Jeannette M. O'Brien, David Mecerreyes, Yi Yan Yang, James L. Hedrick&lt;br/&gt;Catalyst- and isocyanate-free synthesis of polyurethanes in aqueous media.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/MFp80tbGkQg" height="1" width="1"/&gt;</description><a10:updated>2013-03-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haritz Sardon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Amanda C. Engler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Julian M. W. Chan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel J. Coady</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jeannette M. O'Brien</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Mecerreyes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Yan Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">James L. Hedrick</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40319J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36958G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36958G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/XXjhqgL9DGs/C3GC36958G</link><title>A distributed activation energy model for the pyrolysis of lignocellulosic biomass</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36958G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1331-1340&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36958G, Paper&lt;/div&gt;&lt;div&gt;Junmeng Cai, Weixuan Wu, Ronghou Liu, George W. Huber&lt;br/&gt;The pyrolysis kinetics of xylan, cellulose, and eight lignocellulosic biomass samples (including corn stover, cotton stalk, palm oil husk, pine wood, red oak, sugarcane bagasse, switchgrass, and wheat straw) were measured in a TA SDT Q600 thermogravimetric analyzer. A three-parallel-DAEM-reaction model was developed to successfully describe the pyrolysis kinetics of lignocellulosic biomass.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/XXjhqgL9DGs" height="1" width="1"/&gt;</description><a10:updated>2013-03-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Junmeng Cai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Weixuan Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ronghou Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">George W. Huber</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36958G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37030E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37030E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/YuQw9THRoFY/C3GC37030E</link><title>Deep eutectic solvents as extraction media for azeotropic mixtures</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC37030E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1326-1330&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC37030E, Paper&lt;/div&gt;&lt;div&gt;Filipe S. Oliveira, Ana B. Pereiro, Luis P. N. Rebelo, Isabel M. Marrucho&lt;br/&gt;Choline-based Deep Eutectic Solvents were used as highly efficient extractants in the liquid-liquid separation of heptane-ethanol azeotropic mixtures.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/YuQw9THRoFY" height="1" width="1"/&gt;</description><a10:updated>2013-03-15T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Filipe S. Oliveira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ana B. Pereiro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luis P. N. Rebelo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Isabel M. Marrucho</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC37030E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00084B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00084B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/hz8bAjgTZv4/C3GC00084B</link><title>Facile one-pot synthesis of VxOy@C catalysts using sucrose for the direct hydroxylation of benzene to phenol</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00084B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1150-1154&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00084B, Communication&lt;/div&gt;&lt;div&gt;Weitao Wang, Guodong Ding, Tao Jiang, Peng Zhang, Tianbin Wu, Buxing Han&lt;br/&gt;V&lt;small&gt;&lt;sub&gt;&lt;em&gt;x&lt;/em&gt;&lt;/sub&gt;&lt;/small&gt;O&lt;small&gt;&lt;sub&gt;&lt;em&gt;y&lt;/em&gt;&lt;/sub&gt;&lt;/small&gt;@C catalysts prepared from sucrose and NH&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;VO&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; showed satisfactory catalytic performance for the hydroxylation of benzene to phenol in acetonitrile.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/hz8bAjgTZv4" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Weitao Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guodong Ding</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tianbin Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Buxing Han</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00084B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36938B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36938B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/T-wFyUsmWSM/C3GC36938B</link><title>Synthesis and characterization of a renewable polyester containing oxabicyclic dicarboxylate derived from furfural</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36938B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1318-1325&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36938B, Paper&lt;/div&gt;&lt;div&gt;Yuya Tachibana, Masayuki Yamahata, Ken-ichi Kasuya&lt;br/&gt;Furan derivatives produced from inedible biomass resources were converted to novel biomass-based polyesters containing oxabicyclic dicarboxylate.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/T-wFyUsmWSM" height="1" width="1"/&gt;</description><a10:updated>2013-03-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yuya Tachibana</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Masayuki Yamahata</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ken-ichi Kasuya</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36938B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36877G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36877G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/XJDdhAx23EU/C3GC36877G</link><title>Methyl formate as a carbonylating agent for the catalytic conversion of phenol to methyl phenyl carbonate</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36877G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1146-1149&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36877G, Communication&lt;/div&gt;&lt;div&gt;Mohammad S. Yalfani, Giulio Lolli, Aurel Wolf, Leslaw Mleczko, Thomas E. Muller, Walter Leitner&lt;br/&gt;Methyl formate was used as a green and efficient carbonylating agent instead of toxic CO gas in the synthesis of methyl phenyl carbonate from phenol.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/XJDdhAx23EU" height="1" width="1"/&gt;</description><a10:updated>2013-03-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mohammad S. Yalfani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Giulio Lolli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aurel Wolf</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Leslaw Mleczko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas E. Muller</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Walter Leitner</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36877G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40302E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40302E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/O7bv5CvZ1Hs/C3GC40302E</link><title>Environmentally benign peptide synthesis using liquid-assisted ball-milling: application to the synthesis of Leu-enkephalin</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40302E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1116-1120&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40302E, Communication&lt;/div&gt;&lt;div&gt;Julien Bonnamour, Thomas-Xavier Metro, Jean Martinez, Frederic Lamaty&lt;br/&gt;This paper describes an original methodology for peptide bond synthesis avoiding toxic solvents and reactants and its application to the synthesis of Leu-enkephalin.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/O7bv5CvZ1Hs" height="1" width="1"/&gt;</description><a10:updated>2013-03-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Julien Bonnamour</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas-Xavier Metro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean Martinez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frederic Lamaty</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40302E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36754A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36754A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ir10ZlLHjVw/C3GC36754A</link><title>Production of polyetheretherketone in ionic liquid media</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC36754A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1166-1172&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC36754A, Paper&lt;/div&gt;&lt;div&gt;H. Q. Nimal Gunaratne, C. Richard Langrick, Alberto V. Puga, Kenneth R. Seddon, Keith Whiston&lt;br/&gt;Polyetheretherketones were synthesised in the ionic liquid 1-butyl-3-methylimidazolium bis{(trifluoromethyl)sulfonyl}amide and recovered with high separation efficiency.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/ir10ZlLHjVw" height="1" width="1"/&gt;</description><a10:updated>2013-03-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">H. Q. Nimal Gunaratne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C. Richard Langrick</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alberto V. Puga</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kenneth R. Seddon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Keith Whiston</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC36754A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00053B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00053B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/M_DBGI2ulWo/C3GC00053B</link><title>On the usefulness of life cycle assessment in early chemical methodology development: the case of organophosphorus-catalyzed Appel and Wittig reactions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00053B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1255-1263&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00053B, Paper&lt;/div&gt;&lt;div&gt;Henri A. van Kalkeren, Anneloes L. Blom, Floris P. J. T. Rutjes, Mark A. J. Huijbregts&lt;br/&gt;A life cycle assessment (LCA) was conducted in which the classic Appel and Wittig reactions are compared with their catalytic counterparts in terms of cumulative energy demand and greenhouse gas emissions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/M_DBGI2ulWo" height="1" width="1"/&gt;</description><a10:updated>2013-03-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Henri A. van Kalkeren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anneloes L. Blom</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Floris P. J. T. Rutjes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mark A. J. Huijbregts</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00053B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40243F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40243F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/MueJ0w1sEcU/C3GC40243F</link><title>Reduction of sulfoxides and pyridine-N-oxides over iron powder with water as hydrogen source promoted by carbon dioxide</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40243F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1274-1279&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40243F, Paper&lt;/div&gt;&lt;div&gt;Ran Ma, An-Hua Liu, Cheng-Bin Huang, Xue-Dong Li, Liang-Nian He&lt;br/&gt;Reduction of sulfoxides and pyridine-&lt;em&gt;N&lt;/em&gt;-oxides by iron powder performed well in the &lt;em&gt;in situ&lt;/em&gt; acidic CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;-H&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;O system.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/MueJ0w1sEcU" height="1" width="1"/&gt;</description><a10:updated>2013-03-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ran Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">An-Hua Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cheng-Bin Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xue-Dong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liang-Nian He</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40243F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40193F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40193F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/IEpzS9ie0_I/C3GC40193F</link><title>Biocatalysis: fungi mediated novel and selective 12[small beta]- or 17[small beta]-hydroxylation on the basic limonoid skeleton</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC40193F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1311-1317&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC40193F, Paper&lt;/div&gt;&lt;div&gt;Saikat Haldar, Swati P. Kolet, Hirekodathakallu V. Thulasiram&lt;br/&gt;Synthetically challenging, novel and efficient 12[small beta]- and 17[small beta]-hydroxylation was achieved on the basic limonoid skeleton by fungi mediated biocatalysis.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/IEpzS9ie0_I" height="1" width="1"/&gt;</description><a10:updated>2013-03-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Saikat Haldar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Swati P. Kolet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hirekodathakallu V. Thulasiram</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC40193F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00095H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00095H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/swFJTTdy6GE/C3GC00095H</link><title>Synthesis and properties of full bio-based thermosetting resins from rosin acid and soybean oil: the role of rosin acid derivatives</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3GC00095H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;15&lt;/b&gt;,1300-1310&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3GC00095H, Paper&lt;/div&gt;&lt;div&gt;Qiangqiang Ma, Xiaoqing Liu, Ruoyu Zhang, Jin Zhu, Yanhua Jiang&lt;br/&gt;Rosin-based monomers were synthesized and served as petroleum-based rigid compound substitutions to copolymerize with soybean oil derivatives. Full bio-based thermosetting resins were then prepared.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/GC/~4/swFJTTdy6GE" height="1" width="1"/&gt;</description><a10:updated>2013-03-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Qiangqiang Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoqing Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruoyu Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanhua Jiang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/GC/C3GC00095H</feedburner:origLink></item></channel></rss>
