<?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>Tue, 14 Feb 2012 03:02:47 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/2012/GC/C2GC16424H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16424H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/yUWot3VTb7w/C2GC16424H</link><title>CeO2-catalysed one-pot selective synthesis of esters from nitriles and alcohols</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=C2GC16424H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16424H, Paper&lt;/div&gt;&lt;div&gt;Masazumi Tamura, Takuya Tonomura, Ken-ichi Shimizu, Atsushi Satsuma&lt;br/&gt;Thirteen kinds of metal oxides were tested for the one-pot selective synthesis of esters from nitriles and alcohols. Ceria (CeO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;) showed more than two orders of magnitude higher activity than the other oxides.&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/yUWot3VTb7w" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Masazumi Tamura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takuya Tonomura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ken-ichi Shimizu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Atsushi Satsuma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16424H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16264D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16264D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/N6sM-UR3sg4/C2GC16264D</link><title>Single-step catalytic liquid-phase hydroconversion of DCPD into high energy density fuel exo-THDCPD</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=C2GC16264D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16264D, Paper&lt;/div&gt;&lt;div&gt;M. G. Sibi, Bhawan Singh, R. Kumar, C. Pendem, A. K. Sinha&lt;br/&gt;Novel single-step production of jet propellent &lt;i&gt;exo&lt;/i&gt;-tetrahydrodicyclopentadiene &lt;i&gt;via&lt;/i&gt; retro-Diels-Alder reaction at moderate temperature and 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/N6sM-UR3sg4" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">M. G. Sibi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bhawan Singh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">R. Kumar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C. Pendem</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. K. Sinha</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16264D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16082J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16082J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/gYaiHUxBgDY/C2GC16082J</link><title>Biogenic synthesis of photocatalytically active Ag/TiO2 and Au/TiO2 composites</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=C2GC16082J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16082J, Paper&lt;/div&gt;&lt;div&gt;Weibin Liang, Tamara L. Church, Andrew T. Harris&lt;br/&gt;M/TiO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; composites prepared using &lt;i&gt;C&lt;/i&gt;. &lt;i&gt;limon&lt;/i&gt; extract are photocatalysts at least as active as composites prepared using NaBH&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt;.&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/gYaiHUxBgDY" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Weibin Liang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tamara L. Church</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew T. Harris</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16082J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16342J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16342J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/I8bJHTOlVpQ/C2GC16342J</link><title>Electrochemical oxidation of 4-substituted urazoles in the presence of arylsulfinic acids: an efficient method for the synthesis of new sulfonamide 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=C2GC16342J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16342J, Paper&lt;/div&gt;&lt;div&gt;Fahimeh Varmaghani, Davood Nematollahi, Shadpour Mallakpour, Roya Esmaili&lt;br/&gt;Electrosynthesis of new sulfonamide derivatives was carried out &lt;i&gt;via&lt;/i&gt; the electrooxidation of 4-substituted urazoles in the presence of arylsulfinic acids.&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/I8bJHTOlVpQ" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fahimeh Varmaghani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Davood Nematollahi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shadpour Mallakpour</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roya Esmaili</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16342J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16456F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16456F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/dblDldQO3T4/C2GC16456F</link><title>Pd-sodium carboxymethyl cellulose nanocomposites display a morphology dependent response to hydrogen gas</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=C2GC16456F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16456F, Communication&lt;/div&gt;&lt;div&gt;Jianli Zou, K. Swaminathan Iyer, Colin L. Raston&lt;br/&gt;A facile strategy has been developed to alter the response of a hydrogen sensor by changing the morphology of Pd nanocomposites.&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/dblDldQO3T4" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jianli Zou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">K. Swaminathan Iyer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Colin L. Raston</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16456F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC00027J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC00027J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/bIr7QLeOuPU/C2GC00027J</link><title>Catalyst-free approach for solvent-dependent selective oxidation of organic sulfides with oxone</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=C2GC00027J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC00027J, Paper&lt;/div&gt;&lt;div&gt;Bing Yu, An-Hua Liu, Liang-Nian He, Bin Li, Zhen-Feng Diao, Yu-Nong Li&lt;br/&gt;Selective oxidation with oxone to sulfoxides or sulfones can be achieved by changing the solvent without additional catalyst or additive.&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/bIr7QLeOuPU" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bing Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">An-Hua Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liang-Nian He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen-Feng Diao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Nong Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC00027J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16341A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16341A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/eQw3xFbgRvU/C2GC16341A</link><title>Industrial commitment to green and sustainable chemistry: using renewable materials &amp; developing eco-friendly processes and ingredients in cosmetics</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=C2GC16341A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16341A, Paper&lt;/div&gt;&lt;div&gt;Michel Philippe, Blaise Didillon, Laurent Gilbert&lt;br/&gt;This article presents the approach of a cosmetic company regarding the implementation of green chemistry principles and the introduction of green indicators.&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/eQw3xFbgRvU" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Michel Philippe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Blaise Didillon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laurent Gilbert</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16341A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16425F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16425F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/_dJsdchPmuM/C2GC16425F</link><title>Synthesis of novel fused heterocycle-oxa-aza-phenanthrene and anthracene derivatives via sequential one-pot synthesis in aqueous micellar 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=C2GC16425F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16425F, Communication&lt;/div&gt;&lt;div&gt;Madhulika Srivastava, Jaya Singh, Shyam B. Singh, Kamleshwar Tiwari, Vijay K. Pathak, Jagdamba Singh&lt;br/&gt;Oxa-aza-phenanthrene and anthracene derivatives which contain a bridgehead nitrogen are synthesized in an aqueous micellar system. The synthetic route is easy and yield is excellent. In this proposed method, solvent, base and surfactant are optimized and the best result was obtained by DBU in water with surfactant CTAB. This method is an efficient, viable and sequential one pot synthetic route for the construction of desired product.&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/_dJsdchPmuM" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Madhulika Srivastava</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jaya Singh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shyam B. Singh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kamleshwar Tiwari</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vijay K. Pathak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jagdamba Singh</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16425F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16469H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16469H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ObxJwonB3Cg/C2GC16469H</link><title>Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium</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=C2GC16469H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16469H, Paper&lt;/div&gt;&lt;div&gt;Liupan Yang, Daxin Shi, Shu Chen, Hongxin Chai, Danfei Huang, Qi Zhang, Jiarong Li&lt;br/&gt;An efficient and green protocol for synthesis of 2,3-dihydropyrido[2,3-&lt;i&gt;d&lt;/i&gt;]pyrimidin-4(1&lt;i&gt;H&lt;/i&gt;)-ones catalyzed by DBU under microwave irradiation in water has been developed.&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/ObxJwonB3Cg" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Liupan Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daxin Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shu Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongxin Chai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Danfei Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qi Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiarong Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16469H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16389F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16389F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/_FR3xwCUv3Q/C2GC16389F</link><title>New aspects for biomass processing with ionic liquids: towards the isolation of pharmaceutically active betulin</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=C2GC16389F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16389F, Paper&lt;/div&gt;&lt;div&gt;Anna K. Ressmann, Katharina Strassl, Peter Gaertner, Bin Zhao, Lasse Greiner, Katharina Bica&lt;br/&gt;By utilising ionic liquids the pharmaceutically active triterpene betulin can be extracted from biomass with significantly improved extraction yield and purity.&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/_FR3xwCUv3Q" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna K. Ressmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katharina Strassl</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter Gaertner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lasse Greiner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katharina Bica</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16389F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16020J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16020J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/l6zJt3xJy94/C2GC16020J</link><title>Nano rod-shaped and reusable basic Al2O3 catalyst for N-formylation of amines under solvent-free conditions: A novel, practical and convenient 'NOSE' approach</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=C2GC16020J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16020J, Paper&lt;/div&gt;&lt;div&gt;Vijay Kumar Das, Rashmi Rekha Devi, Prasanta Kumar Raul, Ashim Jyoti Thakur&lt;br/&gt;An efficient 'NOSE' protocol for the &lt;i&gt;N&lt;/i&gt;-formylation of amines catalyzed by rod-shaped basic nano Al&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;O&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; has been developed.&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/l6zJt3xJy94" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Vijay Kumar Das</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rashmi Rekha Devi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Prasanta Kumar Raul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ashim Jyoti Thakur</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16020J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16459K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16459K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/h08vtEAsDJg/C2GC16459K</link><title>Patterned growth of nanocrystalline silicon thin films through magnesiothermic reduction of soda lime glass</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=C2GC16459K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16459K, Communication&lt;/div&gt;&lt;div&gt;Deniz P. Wong, Hsiang-Ting Lien, Yit-Tsong Chen, Kuei-Hsien Chen, Li-Chyong Chen&lt;br/&gt;In this study, we report a novel, low-cost and green process in synthesizing nc-Si thin films with the possibility of mass production and pattern formation.&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/h08vtEAsDJg" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Deniz P. Wong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hsiang-Ting Lien</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yit-Tsong Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kuei-Hsien Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Li-Chyong Chen</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16459K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16499J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16499J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ww46S6fmFK0/C2GC16499J</link><title>Thiamine hydrochloride (VB1): an efficient promoter for the one-pot synthesis of benzo[4,5]imidazo[1,2-a]pyrimidine and [1,2,4]triazolo[1,5-a]pyrimidine derivatives in water medium</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=C2GC16499J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16499J, Paper&lt;/div&gt;&lt;div&gt;Junhua Liu, Min Lei, Lihong Hu&lt;br/&gt;An efficient and rapid procedure for the synthesis of benzo[4,5]imidazo[1,2-&lt;i&gt;a&lt;/i&gt;]pyrimidine and [1,2,4]triazolo[1,5-&lt;i&gt;a&lt;/i&gt;]pyrimidine derivatives catalyzed by thiamine hydrochloride (VB&lt;small&gt;&lt;sub&gt;1&lt;/sub&gt;&lt;/small&gt;) in water has been developed.&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/ww46S6fmFK0" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Junhua Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Min Lei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lihong Hu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16499J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16291A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16291A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/sTHr8X55uwY/C2GC16291A</link><title>An atom-efficient synthetic method: carbosilylations of alkenes, alkynes, and cyclic acetals using Lewis and Bronsted acid 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=C2GC16291A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16291A, Critical Review&lt;/div&gt;&lt;div&gt;Ken Motokura, Toshihide Baba&lt;br/&gt;Catalytic allylsilylations and arylsilylations of alkenes, alkynes, and cyclic acetals using homogeneous and heterogeneous Lewis and Bronsted acids are summarized.&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/sTHr8X55uwY" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ken Motokura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Toshihide Baba</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16291A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16503A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16503A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/_zhP-TT9rvg/C2GC16503A</link><title>Natural polyphenols as safe alternatives to hydroquinone for the organocatalyzed reduction of dioxygen dissolved in water by diethylhydroxylamine (DEHA)</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=C2GC16503A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16503A, Paper&lt;/div&gt;&lt;div&gt;Raphael Lebeuf, Ying Zhu, Veronique Nardello-Rataj, Jean-Pierre Lallier, Jean-Marie Aubry&lt;br/&gt;Natural polyphenols as safe alternatives to hydroquinone for the organocatalyzed reduction of dioxygen dissolved in water by diethylhydroxylamine (DEHA).&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/_zhP-TT9rvg" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Raphael Lebeuf</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Veronique Nardello-Rataj</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Pierre Lallier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Marie Aubry</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16503A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16240G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16240G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/yQZFU3Np2xc/C2GC16240G</link><title>Design, synthesis, and solution behaviour of small polyamines as switchable water additives</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=C2GC16240G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16240G, Paper&lt;/div&gt;&lt;div&gt;Sean M. Mercer, Tobias Robert, Daniel V. Dixon, Chien-Shun Chen, Zahra Ghoshouni, Jitendra R. Harjani, Soran Jahangiri, Gilles H. Peslherbe, Philip G. Jessop&lt;br/&gt;Switchable water, an aqueous solvent with switchable ionic strength, requires CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; (as the trigger) and a polyamine ionogen, for which structural design principles are described.&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/yQZFU3Np2xc" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sean M. Mercer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tobias Robert</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel V. Dixon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chien-Shun Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zahra Ghoshouni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jitendra R. Harjani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Soran Jahangiri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gilles H. Peslherbe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Philip G. Jessop</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16240G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16521J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16521J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/kZoEdL0FKV8/C2GC16521J</link><title>Fast, solvent-free and hydrogen-bonding-mediated asymmetric Michael addition in a ball mill</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=C2GC16521J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16521J, Communication&lt;/div&gt;&lt;div&gt;Yi-Feng Wang, Ru-Xiang Chen, Ke Wang, Bin-Bin Zhang, Zhao-Bo Li, Dan-Qian Xu&lt;br/&gt;We report a highly efficient H-bonding-mediated enantioselective Michael addition reaction in a planetary ball mill.&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/kZoEdL0FKV8" height="1" width="1"/&gt;</description><a10:updated>2012-02-09T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yi-Feng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ru-Xiang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ke Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin-Bin Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhao-Bo Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dan-Qian Xu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16521J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16232F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16232F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/1RPbSxSmSSQ/C2GC16232F</link><title>Template-free synthesis of an electroactive Au-Calix-PPY nanocomposite for electrochemical sensor 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=C2GC16232F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16232F, Paper&lt;/div&gt;&lt;div&gt;Shivani Tanwar, Min-Chieh Chuang, K. Sudhakara Prasad, Ja-an Annie Ho&lt;br/&gt;An eco-friendly approach to synthesize the nanocomposite is described, herein. Synthesis parameters were optimized, the material is well characterized, possesses high electrocatalytic activity and applicability as a sensor for formaldehyde and enzyme free glucose detection.&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/~4/1RPbSxSmSSQ" height="1" width="1"/&gt;</description><a10:updated>2012-02-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shivani Tanwar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Min-Chieh Chuang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">K. Sudhakara Prasad</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ja-an Annie Ho</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16232F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16195H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16195H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ckN4bOrcXB0/C2GC16195H</link><title>Power dissipation in microwave-enhanced in situ transesterification of algal biomass to biodiesel</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=C2GC16195H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16195H, Paper&lt;/div&gt;&lt;div&gt;Prafulla D. Patil, Harvind Reddy, Tapaswy Muppaneni, Aravind Mannarswamy, Tanner Schuab, F. Omar Holguin, Peter Lammers, Nagamany Nirmalakhandan, Peter Cooke, Shuguang Deng&lt;br/&gt;We investigated the effect of power dissipation on microwave-accelerated simultaneous extraction and transesterification of dry algal biomass (&lt;i&gt;Nannochloropsis salina&lt;/i&gt;) to biodiesel.&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/ckN4bOrcXB0" height="1" width="1"/&gt;</description><a10:updated>2012-02-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Prafulla D. Patil</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Harvind Reddy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tapaswy Muppaneni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aravind Mannarswamy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tanner Schuab</creator><creator xmlns="http://purl.org/dc/elements/1.1/">F. Omar Holguin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter Lammers</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nagamany Nirmalakhandan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter Cooke</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuguang Deng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16195H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16192C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16192C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/aOXLbZQ1-C0/C2GC16192C</link><title>Halogen-free ultra-high flame retardant polymers through enzyme catalysis</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=C2GC16192C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16192C, Paper&lt;/div&gt;&lt;div&gt;Sethumadhavan Ravichandran, Subhalakshmi Nagarajan, Bon Choel Ku, Bryan Coughlin, Todd Emrick, Jayant Kumar, Ramaswamy Nagarajan&lt;br/&gt;Biocatalytic green polymerization of substituted deoxybenzoins in predominantly aqueous conditions for the synthesis of ultra-high flame retardant poly(deoxybenzoins) with high char forming capability and low heat release capacities.&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/aOXLbZQ1-C0" height="1" width="1"/&gt;</description><a10:updated>2012-02-08T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sethumadhavan Ravichandran</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Subhalakshmi Nagarajan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bon Choel Ku</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bryan Coughlin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Todd Emrick</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jayant Kumar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ramaswamy Nagarajan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16192C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16399C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16399C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/t5qMiut4z9w/C2GC16399C</link><title>Natural biopolymer surface of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-photoinduced modification with triarylsulfonium salts</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=C2GC16399C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16399C, Paper&lt;/div&gt;&lt;div&gt;Davy-Louis Versace, Pierre Dubot, Pierre Cenedese, Jacques Lalevee, Olivier Soppera, Jean-Pierre Malval, Estelle Renard, Valerie Langlois&lt;br/&gt;Efficient green UV-photografting method for modifying PHBHV film in aqueous media to develop biological microdevices.&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/t5qMiut4z9w" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Davy-Louis Versace</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pierre Dubot</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pierre Cenedese</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jacques Lalevee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Soppera</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Pierre Malval</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Estelle Renard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Valerie Langlois</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16399C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16439F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16439F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/YFKH2ZBV-DA/C2GC16439F</link><title>Photooxygenations in a bubble column reactor</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=C2GC16439F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16439F, Communication&lt;/div&gt;&lt;div&gt;Alexander Yavorskyy, Oksana Shvydkiv, Carolin Limburg, Kieran Nolan, Yan M. C. Delaure, Michael Oelgemoller&lt;br/&gt;A novel column reactor was constructed and successfully applied to dye-sensitized photooxygenation reactions in aqueous alcohol solutions.&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/YFKH2ZBV-DA" height="1" width="1"/&gt;</description><a10:updated>2012-02-01T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander Yavorskyy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Oksana Shvydkiv</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carolin Limburg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kieran Nolan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan M. C. Delaure</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Oelgemoller</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16439F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16409D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16409D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/2bAGy4ArhZ8/C2GC16409D</link><title>Recyclable and stable ruthenium catalyst for free radical polymerization at ambient temperature initiated by 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=C2GC16409D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16409D, Communication&lt;/div&gt;&lt;div&gt;Guan Zhang, In Young Song, Taiho Park, Wonyong Choi&lt;br/&gt;A ruthenium complex catalyst immobilized on Nafion coated silica shows recyclable and stable photocatalytic activity for free radical polymerization at mild conditions.&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/~4/2bAGy4ArhZ8" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">In Young Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Taiho Park</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wonyong Choi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16409D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16362D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16362D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/KF6QvB2qDGM/C2GC16362D</link><title>The impact of ionic liquid pretreatment on the chemistry and enzymatic digestibility of Pinus radiata compression wood</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=C2GC16362D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16362D, Paper&lt;/div&gt;&lt;div&gt;Kirk M. Torr, Karen T. Love, Ozgul P. Cetinkol, Lloyd A. Donaldson, Anthe George, Bradley M. Holmes, Blake A. Simmons&lt;br/&gt;Pretreatment with 1-ethyl-3-methylimidazolium acetate induced chemical and structural changes in pine compression wood and improved enzymatic cellulose hydrolysis by 25-fold.&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/KF6QvB2qDGM" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kirk M. Torr</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karen T. Love</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ozgul P. Cetinkol</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lloyd A. Donaldson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anthe George</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bradley M. Holmes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Blake A. Simmons</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16362D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16313F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16313F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/G6JklF0jEjM/C2GC16313F</link><title>An aqueous pathway to polymeric foaming with nanoclay</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=C2GC16313F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16313F, Paper&lt;/div&gt;&lt;div&gt;G. Harikrishnan, Sachchida N. Singh, Chris I. Lindsay, Christopher W. Macosko&lt;br/&gt;A green route for synthesis of foamed polymer nanocomposite is introduced. The technique uses an aqueous route which bypasses the organic surface modification of clay. The use of intermediate solubilization agents for clay dispersion is also avoided.&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/G6JklF0jEjM" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">G. Harikrishnan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sachchida N. Singh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chris I. Lindsay</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher W. Macosko</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16313F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16344F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16344F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/964oTxUuW2Q/C2GC16344F</link><title>Transition metal based catalysts in the aerobic oxidation of alcohols</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=C2GC16344F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16344F, Tutorial Review&lt;/div&gt;&lt;div&gt;Camilla Parmeggiani, Francesca Cardona&lt;br/&gt;Environmentally friendly oxidations of alcohols: implementation of a transition metal-based catalyst with oxygen is an emerging alternative to traditional procedures.&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/~4/964oTxUuW2Q" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Camilla Parmeggiani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francesca Cardona</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16344F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16437J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16437J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/jmMEQSZVPWM/C2GC16437J</link><title>Preparation of clay-supported Sn catalysts and application to Baeyer-Villiger oxidation</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=C2GC16437J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16437J, Paper&lt;/div&gt;&lt;div&gt;Takayoshi Hara, Moriaki Hatakeyama, Arum Kim, Nobuyuki Ichikuni, Shogo Shimazu&lt;br/&gt;Clay-intercalated Sn catalysts show extremely high performance in Bayer-Villiger oxidation and are reusable without any significant loss of activity or selectivity.&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/jmMEQSZVPWM" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Takayoshi Hara</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Moriaki Hatakeyama</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arum Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nobuyuki Ichikuni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shogo Shimazu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16437J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC15946E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC15946E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/C7uvewkT7oo/C2GC15946E</link><title>Efficient conversion of microcrystalline cellulose to 1,2-alkanediols over supported Ni 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=C2GC15946E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC15946E, Paper&lt;/div&gt;&lt;div&gt;Xicheng Wang, Lingqian Meng, Feng Wu, Yijun Jiang, Lei Wang, Xindong Mu&lt;br/&gt;High yield of 1,2-alkanediols can be produced &lt;i&gt;via&lt;/i&gt; one-pot catalytic hydrogenolysis of high-crystalline cellulose over Ni/ZnO catalysts.&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/C7uvewkT7oo" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xicheng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lingqian Meng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yijun Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xindong Mu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC15946E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16364K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16364K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/bBoAz_DqRzI/C2GC16364K</link><title>Catalytic conversion of cellulose to hexitols with mesoporous carbon supported Ni-based 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=C2GC16364K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16364K, Communication&lt;/div&gt;&lt;div&gt;Jifeng Pang, Aiqin Wang, Mingyuan Zheng, Yanhua Zhang, Yanqiang Huang, Xiaowei Chen, Tao Zhang&lt;br/&gt;Robust and highly active Ni-based bimetallic catalysts supported on mesoporous carbon have been developed for catalytic conversion of cellulose to hexitols, over which the maximum hexitol yield reached 59.8%.&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/bBoAz_DqRzI" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jifeng Pang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aiqin Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mingyuan Zheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanhua Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanqiang Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaowei Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16364K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16135D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16135D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/GzAnB-vkbAE/C2GC16135D</link><title>Direct synthesis of unsymmetrical ethers from alcohols catalyzed by titanium cation-exchanged montmorillonite</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=C2GC16135D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16135D, Communication&lt;/div&gt;&lt;div&gt;Takato Mitsudome, Tsuyoshi Matsuno, Shoichiro Sueoka, Tomoo Mizugaki, Koichiro Jitsukawa, Kiyotomi Kaneda&lt;br/&gt;Titanium-exchanged montmorillonite (Ti&lt;small&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;/small&gt;-mont) was found to act as an efficient heterogeneous catalyst for the etherification of various alcohols under mild reaction conditions. Ti&lt;small&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;/small&gt;-mont was reusable and applicable to scale-up conditions.&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/GzAnB-vkbAE" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Takato Mitsudome</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tsuyoshi Matsuno</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shoichiro Sueoka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomoo Mizugaki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koichiro Jitsukawa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kiyotomi Kaneda</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16135D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16517A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16517A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/HxbRoNDdIks/C2GC16517A</link><title>Domino reactions in water: diastereoselective synthesis of densely functionalized indolyldihydrofuran 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=C2GC16517A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16517A, Paper&lt;/div&gt;&lt;div&gt;Pethaiah Gunasekaran, Kamaraj Balamurugan, Sathiyamoorthi Sivakumar, Subbu Perumal, J. Carlos Menendez, Abdulrahman I. Almansour&lt;br/&gt;A library of &lt;i&gt;trans&lt;/i&gt;-5-aroyl-2-(indol-3-yl)-4-aryl-4,5-dihydrofuran-3-carbonitriles was diastereoselectively synthesized in excellent yields from the reaction of 2-(3-indolylcarbonyl)-3-aryl-2-propenenitriles with (2-aryl-2-oxoethyl)pyridinium bromides in the presence of triethylamine &lt;i&gt;via&lt;/i&gt; a simple, user-friendly domino process carried out in water.&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/HxbRoNDdIks" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Pethaiah Gunasekaran</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kamaraj Balamurugan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sathiyamoorthi Sivakumar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Subbu Perumal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">J. Carlos Menendez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abdulrahman I. Almansour</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16517A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16415A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16415A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/uvnxe6yQtTw/C2GC16415A</link><title>A one-pot hydrothermal synthesis of tunable dual heteroatom-doped carbon microspheres</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=C2GC16415A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16415A, Paper&lt;/div&gt;&lt;div&gt;Stephanie-Angelika Wohlgemuth, Filipe Vilela, Maria-Magdalena Titirici, Markus Antonietti&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/uvnxe6yQtTw" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Stephanie-Angelika Wohlgemuth</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Filipe Vilela</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maria-Magdalena Titirici</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Markus Antonietti</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16415A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16428K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16428K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ixv5ZSx6ymk/C2GC16428K</link><title>Production and purification of an extracellular lipolytic enzyme using ionic liquid-based 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=C2GC16428K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16428K, Paper&lt;/div&gt;&lt;div&gt;Sonia Patricia Marques Ventura, Rafael Lemos Freire de Barros, Jose Murillo de Pinho Barbosa, Cleide Mara Faria Soares, Alvaro Silva Lima, Joao Araujo Pereira Coutinho&lt;br/&gt;The successful use of IL-based ATPS as separation techniques for the extraction and purification of enzymes from a fermentation process&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/ixv5ZSx6ymk" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sonia Patricia Marques Ventura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rafael Lemos Freire de Barros</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose Murillo de Pinho Barbosa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cleide Mara Faria Soares</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alvaro Silva Lima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joao Araujo Pereira Coutinho</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16428K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16009A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16009A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/n3cBhAVDedo/C2GC16009A</link><title>Measuring the effect of ionic liquids on laccase activity using a simple, parallel method</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=C2GC16009A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16009A, Paper&lt;/div&gt;&lt;div&gt;Lars Rehmann, Ekaterina Ivanova, Jamie L. Ferguson, H. Q. Nimal Gunaratne, Kenneth R. Seddon, Gillian M. Stephens&lt;br/&gt;Laccases catalyse lignin depolymerisation and numerous other industrially useful processes. Using a new parallel assay, we show that laccase retains activity in the presence of a number of ionic liquids.&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/n3cBhAVDedo" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lars Rehmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ekaterina Ivanova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jamie L. Ferguson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">H. Q. Nimal Gunaratne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kenneth R. Seddon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gillian M. Stephens</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16009A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16259H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16259H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/8iF2vQHWmQU/C2GC16259H</link><title>An in-water, on-water domino process for 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=C2GC16259H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16259H, Communication&lt;/div&gt;&lt;div&gt;Philip Norcott, Calan Spielman, Christopher S. P. McErlean&lt;br/&gt;By exploiting the different aqueous solubility of organic molecules, a domino process involving in-water and on-water chemistry has been developed. Water is utilized as a reaction medium, a product partitioner and a reaction catalyst.&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/~4/8iF2vQHWmQU" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Philip Norcott</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Calan Spielman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher S. P. McErlean</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16259H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16316K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16316K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/f-NLS5Y2CjI/C2GC16316K</link><title>Transamidation of amides with amines under solvent-free conditions using a CeO2 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=C2GC16316K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16316K, Paper&lt;/div&gt;&lt;div&gt;Masazumi Tamura, Takuya Tonomura, Ken-ichi Shimizu, Atsushi Satsuma&lt;br/&gt;Commercial ceria effectively catalyzes transamidation of various primary amides with various amines to yield corresponding &lt;i&gt;N&lt;/i&gt;-alkyl amides under solvent-free conditions.&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/f-NLS5Y2CjI" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Masazumi Tamura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takuya Tonomura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ken-ichi Shimizu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Atsushi Satsuma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16316K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16301B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16301B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/dqzoSLtD_Rs/C2GC16301B</link><title>A highly active magnetically recoverable nano ferrite-glutathione-copper (nano-FGT-Cu) catalyst for Huisgen 1,3-dipolar cycloadditions</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=C2GC16301B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC16301B, Paper&lt;/div&gt;&lt;div&gt;R. B. Nasir Baig, Rajender S. Varma&lt;br/&gt;Magnetically recoverable heterogeneous Cu catalyst has been used for an eco-friendly synthesis of 1,2,3-triazoles &lt;i&gt;via&lt;/i&gt; one-pot multi component reaction using MW irradiation. The catalyst was easily recovered using external magnet and reused in subsequent 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/dqzoSLtD_Rs" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</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/2012/GC/C2GC16301B</feedburner:origLink></item></channel></rss>

