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<?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>Fri, 25 May 2012 12:14:55 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/C2GC35604J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35604J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/XBX_8VNrZ44/C2GC35604J</link><title>Dual Use of a Chemical Auxiliary: Molecularly Imprinted Polymers for the Selective Recovery of Products from Biocatalytic Reaction Mixtures</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35604J, Paper&lt;/div&gt;&lt;div&gt;Aaron T. Larsen, Tiffany Lai, Vanja Polic, Karine Auclair&lt;br/&gt;Auxiliary-directed biocatalysis is a powerful and relatively benign tool for chemical synthesis. We recently reported the use of theobromine as a chemical auxiliary for directing CYP3A4-catalyzed oxidations with predictable regio-,...&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/XBX_8VNrZ44" height="1" width="1"/&gt;</description><a10:updated>2012-05-25T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Aaron T. Larsen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tiffany Lai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vanja Polic</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karine Auclair</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35604J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35225G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35225G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/gf5k0Xn1o2s/C2GC35225G</link><title>Organic-inorganic hybrid porous sulfonated zinc phosphonate material: efficient catalyst for biodiesel synthesis at room temperature</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35225G, Paper&lt;/div&gt;&lt;div&gt;Asim Bhaumik, Malay Pramanik, Mahasweta Nandi, Hiroshi Uyama&lt;br/&gt;A new porous zinc phosphonate material (HZnP-1) has been synthesized through the reaction of p-xylenediphosphonic acid and anhydrous ZnCl2 under hydrothermal condition at mildly acidic condition (pH~5)in the absence of...&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/gf5k0Xn1o2s" height="1" width="1"/&gt;</description><a10:updated>2012-05-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Asim Bhaumik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Malay Pramanik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mahasweta Nandi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hiroshi Uyama</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35225G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35619H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35619H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/LnqlrwqUYLE/C2GC35619H</link><title>Lanthanide Replacement in Organic Synthesis: Luche-Type Reduction of [small alpha],[small beta]-Unsaturated Ketones in the Presence of Calcium triflate</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35619H, Communication&lt;/div&gt;&lt;div&gt;Nina Forkel, David Henderson, Matthew Fuchter&lt;br/&gt;Development of a calcium-mediated regioselective 1,2-reduction of challenging [small alpha],[small beta]-unsaturated ketones, such as 2-cyclopententone, is reported. The corresponding allylic alcohols are obtained in very good regioselectivities using Ca(OTf)2 and NaBH4. Furthermore,...&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/LnqlrwqUYLE" height="1" width="1"/&gt;</description><a10:updated>2012-05-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nina Forkel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Henderson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew Fuchter</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35619H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35424A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35424A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/pkpmBf3AuWk/C2GC35424A</link><title>Elimination of the negative effect of nitrogen compounds by CO2/water in the hydrocracking of anthracene</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35424A, Communication&lt;/div&gt;&lt;div&gt;Buxing Han, Honglei Fan, Qian Wang, Jin Guo, Tao Jiang, Zhaofu Zhang, Guanying Yang&lt;br/&gt;Development of green and efficient methods to eliminate the negative effect of the nitrogen compounds in the hydrocracking of heavy oils is of great importance, and model compounds (e.g. anthracene)...&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/pkpmBf3AuWk" height="1" width="1"/&gt;</description><a10:updated>2012-05-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Buxing Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Honglei Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qian Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhaofu Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guanying Yang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35424A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35615E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35615E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/-4_eW_4rQSA/C2GC35615E</link><title>[small omega]-Transaminase-catalyzed kinetic resolution of chiral amines using L-threonine as an amino acceptor precursor</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35615E, Communication&lt;/div&gt;&lt;div&gt;M. Shaheer Malik, Eul-Soo Park, Jong-Shik Shin&lt;br/&gt;Cost-effective kinetic resolution of chiral amines using L-threonine as a cosubstrate was demonstrated by a biocatalytic strategy in which (S)-selective [small omega]-transaminase ([small omega]-TA) was coupled with threonine deaminase (TD), eliminating 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/-4_eW_4rQSA" height="1" width="1"/&gt;</description><a10:updated>2012-05-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">M. Shaheer Malik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eul-Soo Park</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jong-Shik Shin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35615E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35302D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35302D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/cFmUQIPAYdM/C2GC35302D</link><title>PdCl2(py)2 encaged in monodispersed zeolitic hollow spheres: a highly efficient and reusable catalyst for Suzuki-Miyaura cross-coupling reaction 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=C2GC35302D" /&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/C2GC35302D, Paper&lt;/div&gt;&lt;div&gt;Zhenhong Guan, Jianglin Hu, Yanlong Gu, Haojun Zhang, Guangxing Li, Tao Li&lt;br/&gt;Silicalite-1 hollow spheres as "containers" for PdCl&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;(py)&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; represent one of the most efficient heterogeneous systems in Suzuki-Miyaura 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/cFmUQIPAYdM" height="1" width="1"/&gt;</description><a10:updated>2012-05-21T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhenhong Guan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianglin Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanlong Gu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haojun Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guangxing Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35302D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35343A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35343A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ksuU9DwOrn8/C2GC35343A</link><title>Triacetic acid lactone as a potential biorenewable platform chemical</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=C2GC35343A" /&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/C2GC35343A, Communication&lt;/div&gt;&lt;div&gt;Mei Chia, Thomas J. Schwartz, Brent H. Shanks, James A. Dumesic&lt;br/&gt;Triacetic acid lactone is a versatile biorenewable molecule with potential as a platform chemical for the production of valuable bifunctional chemical intermediates and end products, such as sorbic acid.&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/ksuU9DwOrn8" height="1" width="1"/&gt;</description><a10:updated>2012-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mei Chia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas J. Schwartz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Brent H. Shanks</creator><creator xmlns="http://purl.org/dc/elements/1.1/">James A. Dumesic</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35343A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35168D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35168D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/LeZ9mLDuqEI/C2GC35168D</link><title>Zeolite supported Bronsted-acid ionic liquids: an eco approach for synthesis of spiro[indole-pyrido[3,2-e]thiazine] in water under ultrasonication</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=C2GC35168D" /&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/C2GC35168D, Paper&lt;/div&gt;&lt;div&gt;Kapil Arya, Diwan Singh Rawat, Hiroaki Sasai&lt;br/&gt;Ultrasound-promoted novel protocol has been developed for spiro heterocycles. Those reluctant to be formed under conventional conditions, can be prepared by one pot cyclocondensation reaction between &lt;em&gt;N&lt;/em&gt;-substituted isatin and amines with 2-mercaptonicotinic acid in the presence of a novel ZSM-5-zeolite Bronsted-acid catalyst system 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/LeZ9mLDuqEI" height="1" width="1"/&gt;</description><a10:updated>2012-04-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kapil Arya</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Diwan Singh Rawat</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hiroaki Sasai</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35168D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16652F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16652F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/wGjAbstj92I/C2GC16652F</link><title>Ionic liquids as foaming agents of semi-crystalline natural-based polymers</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=C2GC16652F" /&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/C2GC16652F, Paper&lt;/div&gt;&lt;div&gt;Ana Rita C. Duarte, Simone S. Silva, Joao F. Mano, Rui L. Reis&lt;br/&gt;In this work the design and development of new 3D architectures of natural-based polymers, namely a starch polycaprolactone blend was achieved by combining ionic liquids (ILs) and supercritical fluid (SCF) technology. To our knowledge it is the first time that ILs, which have recently been proposed as plasticizing agents, were used as foaming agents.&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/wGjAbstj92I" height="1" width="1"/&gt;</description><a10:updated>2012-05-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ana Rita C. Duarte</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Simone S. Silva</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joao F. Mano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rui L. Reis</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16652F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35272A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35272A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/t04Evjw_alc/C2GC35272A</link><title>Probing the microwave interaction mechanisms and reaction pathways in the energy-efficient, ultra-rapid synthesis of tungsten carbide</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35272A, Paper&lt;/div&gt;&lt;div&gt;Simon Vallance, Helen Kitchen, Clemens Ritter, Samuel Kingman, Georgios Dimitrakis, Duncan Gregory&lt;br/&gt;Tungsten carbide, WC, can be prepared by microwave (MW) synthesis in the solid state from its component elements in air on timescales that are orders of magnitude faster than those...&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/t04Evjw_alc" height="1" width="1"/&gt;</description><a10:updated>2012-05-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Simon Vallance</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helen Kitchen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Clemens Ritter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samuel Kingman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Georgios Dimitrakis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Duncan Gregory</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35272A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35256G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35256G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/grmbfiC7tsY/C2GC35256G</link><title>Construction of a quinoline ring via a 3-component reaction in water: crystal structure analysis and H-bonding patterns of a 2-aryl quinoline</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=C2GC35256G" /&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/C2GC35256G, Communication&lt;/div&gt;&lt;div&gt;T. Ram Reddy, L. Srinivasula Reddy, G. Rajeshwar Reddy, Kaviraj Yarbagi, Y. Lingappa, D. Rambabu, G. Rama Krishna, C. Malla Reddy, K. Shiva Kumar, Manojit Pal&lt;br/&gt;We describe green synthesis of 2-substituted quinolines &lt;em&gt;via&lt;/em&gt; a 3-component reaction in water along with the crystal structure analysis of a 2-arylquinoline.&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/grmbfiC7tsY" height="1" width="1"/&gt;</description><a10:updated>2012-04-25T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">T. Ram Reddy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">L. Srinivasula Reddy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">G. Rajeshwar Reddy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kaviraj Yarbagi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Y. Lingappa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">D. Rambabu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">G. Rama Krishna</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C. Malla Reddy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">K. Shiva Kumar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manojit Pal</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35256G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35214A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35214A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/c-BqIVbfqew/C2GC35214A</link><title>A new route for the synthesis of methacrylic acid from 2-methyl-1,3-propanediol by integrating biotransformation and catalytic dehydration</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=C2GC35214A" /&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/C2GC35214A, Paper&lt;/div&gt;&lt;div&gt;Sang-Hyun Pyo, Tarek Dishisha, Secil Dayankac, Jargalan Gerelsaikhan, Stefan Lundmark, Nicola Rehnberg, Rajni Hatti-Kaul&lt;br/&gt;Methacrylic acid was produced in high yield by an integrated process involving bioconversion of 2-methyl-1,3-propanediol to 3-hydroxy-2-methylpropionic acid 3-hydroxy-2-methylpropanal, and catalytic dehydration of the resulting acid.&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/c-BqIVbfqew" height="1" width="1"/&gt;</description><a10:updated>2012-04-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sang-Hyun Pyo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tarek Dishisha</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Secil Dayankac</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jargalan Gerelsaikhan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan Lundmark</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicola Rehnberg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rajni Hatti-Kaul</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35214A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35444F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35444F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ZzKqS_ZpBho/C2GC35444F</link><title>Carbonic Anhydrase Assisted Calcium Carbonate Crystalline Composites as a Biocatalyst</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35444F, Paper&lt;/div&gt;&lt;div&gt;Ee Taek Hwang, Haemin Gang, Jinyang Chung, Man bock Gu&lt;br/&gt;In the present study, we report on the carbonic anhydrase (CA)-assisted formation of biomineralized calcium carbonate crystalline composites (CCCCs). Ellipsoidal CCCCs, such as calcite polymorphism, in a micro-size range catalyzed...&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/ZzKqS_ZpBho" height="1" width="1"/&gt;</description><a10:updated>2012-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ee Taek Hwang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haemin Gang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinyang Chung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Man bock Gu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35444F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35261C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35261C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/RsP7voSgflg/C2GC35261C</link><title>Water-soluble hyperbranched poly(ester urethane)s based on D,L-alanine: isocyanate-free synthesis, post-functionalization and application</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35261C, Paper&lt;/div&gt;&lt;div&gt;Youmei Bao, guorong Shen, Jing He, Yuesheng Li Li&lt;br/&gt;Green synthesis of a novel hyperbranched poly(ester urethane) (HBPEU) derived from D,L-alanine and an environment-friendly cyclic carbonate monomer, glycerol carbonate, has been reported via an isocyanate-free method. Benefited from 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/RsP7voSgflg" height="1" width="1"/&gt;</description><a10:updated>2012-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Youmei Bao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">guorong Shen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuesheng Li Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35261C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35559K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35559K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/u2OIoLWc3xk/C2GC35559K</link><title>Immobilization and stabilization of subtilisin Carlsberg in magnetically-separable mesoporous silica for the transesterification in an organic solvent</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35559K, Communication&lt;/div&gt;&lt;div&gt;Ee Taek Hwang, Byoungsoo Lee, Meiling Zhang, Seung-Hyun Jun, Jongmin Shim, Jinwoo Lee, Jungbae Kim, Man bock Gu&lt;br/&gt;Subtilisin Carlsberg (SC) was immobilized and stabilized in magnetically-separable mesoporous silica (Mag-MSU-F) in a form of nanoscale enzyme reactors (NERs) based on the ship-in-a-bottle mechanism. Stablized NERs of SC (NER-SC)...&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/u2OIoLWc3xk" height="1" width="1"/&gt;</description><a10:updated>2012-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ee Taek Hwang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Byoungsoo Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meiling Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Seung-Hyun Jun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jongmin Shim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinwoo Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jungbae Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Man bock Gu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35559K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35485C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35485C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/oG3bUPyuZb0/C2GC35485C</link><title>Isopropenyl acetate, a remarkable, cheap and acylating agent of amines under solvent- and catalyst-free conditions: a systematic investigation.</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35485C, Paper&lt;/div&gt;&lt;div&gt;Romina Pelagalli, Isabella Chiarotto, Marta Feroci, Stefano Vecchio&lt;br/&gt;Isopropenyl acetate was proved to be an efficient reagent for acetylation of amine in the absence of solvent and catalyst. The corresponding acetamides were obtained in very high yields without...&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/oG3bUPyuZb0" height="1" width="1"/&gt;</description><a10:updated>2012-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Romina Pelagalli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Isabella Chiarotto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marta Feroci</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefano Vecchio</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35485C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35160A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35160A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/W9ZPoiSG4qI/C2GC35160A</link><title>Evolution of asymmetric organocatalysis: multi- and retrocatalysis</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=C2GC35160A" /&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/C2GC35160A, Critical Review&lt;/div&gt;&lt;div&gt;Raffael C. Wende, Peter R. Schreiner&lt;br/&gt;Combining multiple organocatalysts with orthogonal reactivity for one-pot multistep reaction sequences leads to significantly improved reaction and resource efficiency - a review.&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/W9ZPoiSG4qI" height="1" width="1"/&gt;</description><a10:updated>2012-03-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Raffael C. Wende</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter R. Schreiner</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35160A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35419E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35419E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Q6jbofXeK_Y/C2GC35419E</link><title>Synthesis of C6-Azolyl Purine Nucleosides via C-N Coupling Reaction of Unprotected 6-Chloropurine Nucleosides and N-Heterocycles under Catalyst- and Solvent-Free Condition</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35419E, Communication&lt;/div&gt;&lt;div&gt;Haiming Guo, Guirong Qu, Hongying Niu&lt;br/&gt;C6-Azolyl purine nucleosides products are prepared in high yields under solvent- and catalyst-free conditions via C-N coupling reaction of unprotected 6-chloropurine nucleosides and N-heterocycles, providing a unifying, simple and environmentally...&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/Q6jbofXeK_Y" height="1" width="1"/&gt;</description><a10:updated>2012-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haiming Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guirong Qu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongying Niu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35419E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35483G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35483G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/lyCkQg-IBo0/C2GC35483G</link><title>Efficient and reusable amine-functionalized polyacrylonitrile fiber catalysts for Knoevenagel condensation in water</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35483G, Paper&lt;/div&gt;&lt;div&gt;Guowei Li, Jia Xiao, Wenqin Zhang&lt;br/&gt;A series of new fiber catalysts has been synthesized by aminating a commercially available polyacrylonitrile fiber with polyamines such as diethylenetriamine and triethylenetetramine. These fiber catalysts can efficiently catalyze 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/lyCkQg-IBo0" height="1" width="1"/&gt;</description><a10:updated>2012-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guowei Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jia Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenqin Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35483G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35509D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35509D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/SdRf6Lk39m4/C2GC35509D</link><title>Preparation and characterization of bioplastics made from cottonseed protein</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35509D, Paper&lt;/div&gt;&lt;div&gt;Hangbo Yue, Yingde Cui, Peter S. Shuttleworth, Prof James Clark&lt;br/&gt;Cottonseed protein bioplastics (CPBs) from cottonseed flour were successfully prepared by hot-press molding in the presence of urea, aldehydes and glycerol. The effect of cross-linking treatment on the thermal stability,...&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/SdRf6Lk39m4" height="1" width="1"/&gt;</description><a10:updated>2012-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hangbo Yue</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yingde Cui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter S. Shuttleworth</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Prof James Clark</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35509D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35426H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35426H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/X_zExJlagwQ/C2GC35426H</link><title>Bio-oil upgrading at ambient pressure and temperature using zero valent metals</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35426H, Paper&lt;/div&gt;&lt;div&gt;Wu-Jun Liu, Xue-Song Zhang, Hong Jiang, Yan-Chao Qv, Han-qing Yu&lt;br/&gt;As a liquid product from fast pyrolysis of renewable biomass, bio-oil has a great potential use as fuel or high-value chemicals resource, but it is accompanied with the inherent drawbacks...&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/X_zExJlagwQ" height="1" width="1"/&gt;</description><a10:updated>2012-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wu-Jun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xue-Song Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan-Chao Qv</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Han-qing Yu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35426H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35105F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35105F</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/n5NuSp-3vpI/C2GC35105F</link><title>Simultaneous delignification and selective catalytic transformation of agricultural lignocellulose in cooperative ionic liquid pairs</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=C2GC35105F" /&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/C2GC35105F, Paper&lt;/div&gt;&lt;div&gt;Jinxing Long, Xuehui Li, Bin Guo, Furong Wang, Yinghao Yu, Lefu Wang&lt;br/&gt;An efficient liquefaction and selective delignification process for lignocelluloses was achieved based on a dissolution and &lt;em&gt;in situ&lt;/em&gt; catalysis mechanism.&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/n5NuSp-3vpI" height="1" width="1"/&gt;</description><a10:updated>2012-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jinxing Long</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuehui Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Furong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yinghao Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lefu Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35105F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35071H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35071H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/9u6UX6ZCABY/C2GC35071H</link><title>Ionic liquid-functionalized biochar sulfonic acid as a biomimetic catalyst for hydrolysis of cellulose and bamboo under microwave irradiation</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=C2GC35071H" /&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/C2GC35071H, Paper&lt;/div&gt;&lt;div&gt;Chao Zhang, Zaihui Fu, Ya Chun Liu, Baohua Dai, Yanhong Zou, Xinglang Gong, Yanlong Wang, Xiaolin Deng, Haitao Wu, Qiong Xu, Kirk R. Steven, Dulin Yin&lt;br/&gt;Ionic liquid-functionalized biochar sulfonic acid (BC-SO&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;H-IL) was found to be an efficient biomimetic catalyst for microwave-assisted heterogeneous hydrolysis of cellulose.&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/~4/9u6UX6ZCABY" height="1" width="1"/&gt;</description><a10:updated>2012-04-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chao Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zaihui Fu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ya Chun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baohua Dai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanhong Zou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinglang Gong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanlong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaolin Deng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haitao Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiong Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kirk R. Steven</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dulin Yin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35071H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35337G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35337G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/L9vKv-6-tKg/C2GC35337G</link><title>Iodine-Catalyzed Oxidative System for 3-Sulfenylation of Indoles with Disulfides using DMSO as oxidant under Ambient Conditions In Dimethyl Carbonate</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35337G, Paper&lt;/div&gt;&lt;div&gt;Wenlei Ge, Yunyang Wei&lt;br/&gt;The iodine catalyzed oxidative system for 3-sulfenylation of indoles with disulfides using DMSO has been achieved under ambient conditions, providing a highly convenient and efficient method for the synthesis of...&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/L9vKv-6-tKg" height="1" width="1"/&gt;</description><a10:updated>2012-05-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wenlei Ge</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yunyang Wei</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35337G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35305A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35305A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/jHCnHSME9bw/C2GC35305A</link><title>Robust eco-friendly protocol for the preparation of [gamma]-hydroxy-[small alpha],[small beta]-acetylenic esters by sequential one-pot elimination-addition of 2-bromoacrylates to aldehydes promoted by LTMP in 2-MeTHF</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=C2GC35305A" /&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/C2GC35305A, Communication&lt;/div&gt;&lt;div&gt;Vittorio Pace, Laura Castoldi, Andres R. Alcantara, Wolfgang Holzer&lt;br/&gt;[gamma]-Hydroxy-[small alpha],[small beta]-acetylenic esters are synthesized directly from 2-bromoacrylic esters and aldehydes with LTMP in the biomass-derived solvent 2-MeTHF.&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/jHCnHSME9bw" height="1" width="1"/&gt;</description><a10:updated>2012-04-25T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Vittorio Pace</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laura Castoldi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andres R. Alcantara</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wolfgang Holzer</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35305A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16462K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16462K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/uGo9eDTiyJI/C2GC16462K</link><title>A structured catalyst based on cobalt phthalocyanine/calcined Mg-Al hydrotalcite film for the oxidation of mercaptan</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=C2GC16462K" /&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/C2GC16462K, Paper&lt;/div&gt;&lt;div&gt;Zhiyong Sun, Lan Jin, Shan He, Yufei Zhao, Min Wei, David G. Evans, Xue Duan&lt;br/&gt;A CoPcS/MMO structured catalyst was fabricated, which shows high catalytic activity, good recyclability and easy manipulation for the mercaptan sweetening 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/uGo9eDTiyJI" height="1" width="1"/&gt;</description><a10:updated>2012-05-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiyong Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lan Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shan He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yufei Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Min Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David G. Evans</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xue Duan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16462K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35148J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35148J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/NF0AJ5ORhTc/C2GC35148J</link><title>Metal-free oxidation of sulfides by carbon nitride with visible light illumination at room temperature</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=C2GC35148J" /&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/C2GC35148J, Paper&lt;/div&gt;&lt;div&gt;Pengfei Zhang, Yong Wang, Haoran Li, Markus Antonietti&lt;br/&gt;Mpg-C&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;N&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt; has been successfully utilized as an metal-free catalyst, especially for coupling with aldehydes, in the visible-light-induced oxidation of sulfides by O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; under mild conditions (25 [degree]C, O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; 1 atm).&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/NF0AJ5ORhTc" height="1" width="1"/&gt;</description><a10:updated>2012-05-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Pengfei Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haoran Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Markus Antonietti</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35148J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35410A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35410A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/YqLzN6xUIp0/C2GC35410A</link><title>Mechanosynthesis of nitrosobenzenes: a proof-of-principle study in combining solvent-free synthesis with solvent-free separations</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=C2GC35410A" /&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/C2GC35410A, Communication&lt;/div&gt;&lt;div&gt;Igor Huskic, Ivan Halasz, Tomislav Friscic, Hrvoj Vancik&lt;br/&gt;Selective and completely solvent-free solid-state mechanochemical oxidation of anilines to nitrosobenzenes fills the gap in the solid-state interconversions of nitrogen-based organic functionalities.&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/YqLzN6xUIp0" height="1" width="1"/&gt;</description><a10:updated>2012-04-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Igor Huskic</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ivan Halasz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomislav Friscic</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hrvoj Vancik</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35410A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35321K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35321K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/plJwUY6RTs8/C2GC35321K</link><title>Selective recovery of gold using some cross-linked polysaccharide gels</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=C2GC35321K" /&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/C2GC35321K, Paper&lt;/div&gt;&lt;div&gt;Bimala Pangeni, Hari Paudyal, Minoru Abe, Katsutoshi Inoue, Hidetaka Kawakita, Keisuke Ohto, Birendra Babu Adhikari, Shafiq Alam&lt;br/&gt;Effective recovery of gold from aqueous acidic chloride media was achieved with different kinds of polysaccharides with different structures by treating with concentrated sulfuric acid.&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/plJwUY6RTs8" height="1" width="1"/&gt;</description><a10:updated>2012-04-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bimala Pangeni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hari Paudyal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minoru Abe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katsutoshi Inoue</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hidetaka Kawakita</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Keisuke Ohto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Birendra Babu Adhikari</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shafiq Alam</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35321K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35126A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35126A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/9jV8PV68Xgg/C2GC35126A</link><title>An insight into solvent-free diimide porphyrin reduction: a versatile approach for meso-aryl hydroporphyrin 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=C2GC35126A" /&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/C2GC35126A, Paper&lt;/div&gt;&lt;div&gt;Mariette M. Pereira, Artur R. Abreu, Nuno P. F. Goncalves, Mario J. F. Calvete, Ana V. C. Simoes, Carlos J. P. Monteiro, Luis G. Arnaut, Maria Ermelinda Eusebio, Joao Canotilho&lt;br/&gt;Environmentally sustainable synthetic method for the preparation of &lt;em&gt;meso&lt;/em&gt;-aryl hydroporphyrins, &lt;em&gt;via&lt;/em&gt; reduction of porphyrins with diimide, in the total absence of solvents and bases. Thermomicroscopy studies clearly showed that the process is a typical solvent-free reaction.&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/~4/9jV8PV68Xgg" height="1" width="1"/&gt;</description><a10:updated>2012-03-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mariette M. Pereira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Artur R. Abreu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nuno P. F. Goncalves</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mario J. F. Calvete</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ana V. C. Simoes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carlos J. P. Monteiro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luis G. Arnaut</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maria Ermelinda Eusebio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joao Canotilho</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35126A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35401B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35401B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/NJjtZl1g1mw/C2GC35401B</link><title>An efficient protocol for palladium-catalyzed ligand-free Suzuki-Miyaura coupling in water</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35401B, Communication&lt;/div&gt;&lt;div&gt;Manoj Mondal, Utpal Bora&lt;br/&gt;An in situ generated catalytic system based on PdCl2 and sodium sulfate exhibited excellent catalytic activity in the Suzuki-Miyaura cross-coupling reactions of aryl halides with arylboronic acids at room temperature...&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/NJjtZl1g1mw" height="1" width="1"/&gt;</description><a10:updated>2012-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Manoj Mondal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Utpal Bora</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35401B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35445D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35445D</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/99JNHvIKOhI/C2GC35445D</link><title>Aromatic C-N bond formation via simultaneous activation of C-H and N-H bonds: direct oxyamination of benzene to aniline</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35445D, Communication&lt;/div&gt;&lt;div&gt;Bin Guo, Qian Zhang, Guiying Li, Junyi Yao, Changwei Hu&lt;br/&gt;We develop a new method to directly synthesize aniline from benzene and aqueous ammonia with hydrogen peroxide over Cu/TS-1 catalyst. Formation of Cu-O-Ti species on catalyst promotes the chemical adsorption...&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/~4/99JNHvIKOhI" height="1" width="1"/&gt;</description><a10:updated>2012-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qian Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guiying Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junyi Yao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Changwei Hu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35445D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35457H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35457H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/E1wh3lIh7Zk/C2GC35457H</link><title>Iron-catalyzed arylation of benzoazoles with aromatic aldehydes using oxygen as oxidant</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=C2GC35457H" /&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/C2GC35457H, Communication&lt;/div&gt;&lt;div&gt;Saiwen Liu, Ru Chen, Xiangyu Guo, Huiqiong Yang, Guojun Deng, Chao-Jun Li&lt;br/&gt;Iron-catalyzed oxidative arylation of benzoazoles with aromatic aldehydes.&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/E1wh3lIh7Zk" height="1" width="1"/&gt;</description><a10:updated>2012-04-25T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Saiwen Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ru Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangyu Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huiqiong Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guojun Deng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chao-Jun Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35457H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35318K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35318K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/8eaGvSGrNb8/C2GC35318K</link><title>Different ionic liquids favor different lignocellulosic biomass particle sizes during pretreatment to function efficiently</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=C2GC35318K" /&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/C2GC35318K, Paper&lt;/div&gt;&lt;div&gt;Erinc Bahcegul, Serpil Apaydin, Nazife Isik Haykir, Emre Tatli, Ufuk Bakir&lt;br/&gt;Cotton stalks were ground to four different particle sizes and subjected to preteatment &lt;em&gt;via&lt;/em&gt; two different ionic liquids. The optimum particle size was different for each ionic liquid in terms of the glucose yields obtained upon the enzymatic hydrolysis of pretreated cotton stalks.&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/~4/8eaGvSGrNb8" height="1" width="1"/&gt;</description><a10:updated>2012-04-25T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Erinc Bahcegul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Serpil Apaydin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nazife Isik Haykir</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emre Tatli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ufuk Bakir</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35318K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35219B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35219B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/_RBkcqMU-GI/C2GC35219B</link><title>Transforming animal fats into biodiesel using charcoal 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=C2GC35219B" /&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/C2GC35219B, Paper&lt;/div&gt;&lt;div&gt;Eilhann E. Kwon, Jaegun Seo, Haakrho Yi&lt;br/&gt;This study confirmed that the main driving force of biodiesel conversion through the non-catalytic transesterification reaction is temperature rather than 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/_RBkcqMU-GI" height="1" width="1"/&gt;</description><a10:updated>2012-04-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Eilhann E. Kwon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jaegun Seo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haakrho Yi</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35219B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35246J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35246J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/u_KO5_c1UMM/C2GC35246J</link><title>An environmentally friendlier approach to hydrometallurgy: highly selective separation of cobalt from nickel by solvent extraction with undiluted phosphonium 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=C2GC35246J" /&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/C2GC35246J, Paper&lt;/div&gt;&lt;div&gt;Sil Wellens, Ben Thijs, Koen Binnemans&lt;br/&gt;Cobalt can efficiently be separated from nickel by solvent extraction with the ionic liquid tri(hexyl)tetradecylphosphonium chloride.&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/u_KO5_c1UMM" height="1" width="1"/&gt;</description><a10:updated>2012-04-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sil Wellens</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ben Thijs</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koen Binnemans</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35246J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35289C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35289C</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/5ZyebEHJN9k/C2GC35289C</link><title>A comparative study of different metal acetylacetonates covalently anchored onto amine functionalized silica: a study of the oxidation of aldehydes and alcohols to corresponding acids 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=C2GC35289C" /&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/C2GC35289C, Paper&lt;/div&gt;&lt;div&gt;Ravinderpal Kour Sodhi, Satya Paul, J. H. Clark&lt;br/&gt;A series of different supported metal acetylacetonates were prepared and their catalytic activity was evaluated for the oxidation of aldehydes and benzyl alcohols to the corresponding carboxylic acids in aqueous medium.&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/~4/5ZyebEHJN9k" height="1" width="1"/&gt;</description><a10:updated>2012-04-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ravinderpal Kour Sodhi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Satya Paul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">J. H. Clark</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35289C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35293A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35293A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/FIxISPKULzo/C2GC35293A</link><title>Gold-catalyzed tandem reaction in water: an efficient and convenient synthesis of fused polycyclic indoles</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=C2GC35293A" /&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/C2GC35293A, Paper&lt;/div&gt;&lt;div&gt;Enguang Feng, Yu Zhou, Fei Zhao, Xianjie Chen, Lei Zhang, Hualiang Jiang, Hong Liu&lt;br/&gt;This "on water" protocol proceeds in high atom economy and leads to the generation of two rings, together with the formation of one new C-C bond and two new C-N bonds in a single operation.&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/FIxISPKULzo" height="1" width="1"/&gt;</description><a10:updated>2012-04-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Enguang Feng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fei Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xianjie Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hualiang Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35293A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35222B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35222B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/2Z5RPpM40ZE/C2GC35222B</link><title>Efficient removal of gold complexes from water by precipitation or liquid-liquid extraction using ionic liquids</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35222B, Paper&lt;/div&gt;&lt;div&gt;Nicolas Papaiconomou, Ghislain Vite, Nicolas Goujon, Jean-Marc LEVEQUE, Isabelle Billard&lt;br/&gt;Extraction of tetrachloroaurate or tetrabromoaurate anions has been carried out at pH (1 and 3 to 4) with several ionic liquids bearing halide or bis(trifluoromethanesulfonyl)imide NTf2- anions and 1-octyl-3-methylimidazolium, 1-octylpyridinium...&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/~4/2Z5RPpM40ZE" height="1" width="1"/&gt;</description><a10:updated>2012-05-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nicolas Papaiconomou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ghislain Vite</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicolas Goujon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Marc LEVEQUE</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Isabelle Billard</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35222B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35270B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35270B</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/AOOvonKvWNI/C2GC35270B</link><title>Magnetic separation of fatty acids with iron oxide nanoparticles and application to extractive deacidification of vegetable oils</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=C2GC35270B" /&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/C2GC35270B, Paper&lt;/div&gt;&lt;div&gt;Manuel Cano, Kamal Sbargoud, Emmanuel Allard, Chantal Larpent&lt;br/&gt;Facile, eco-friendly removal of free fatty acids from vegetable oils using magnetite nanoparticles: a cheap, non-toxic, easy to separate and recyclable adsorbent.&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/AOOvonKvWNI" height="1" width="1"/&gt;</description><a10:updated>2012-04-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Manuel Cano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kamal Sbargoud</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emmanuel Allard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chantal Larpent</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35270B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35243E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35243E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/ZJaHyDpoTh8/C2GC35243E</link><title>Solvent- and catalyst-free synthesis of new hydroxylated trisubstituted pyridines under microwave irradiation</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=C2GC35243E" /&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/C2GC35243E, Paper&lt;/div&gt;&lt;div&gt;Guodong Yin, Qiong Liu, Junrui Ma, Nengfang She&lt;br/&gt;New hydroxylated pyridine derivatives were synthesized under solvent-free, catalyst-free and microwave irradiation conditions without protection of the hydroxyl group.&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/ZJaHyDpoTh8" height="1" width="1"/&gt;</description><a10:updated>2012-04-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guodong Yin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiong Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junrui Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nengfang She</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35243E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35306G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35306G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/vrjvaspQ_vY/C2GC35306G</link><title>Effective saccharification of lignocellulosic biomass over hydrolysis residue derived solid acid under microwave irradiation</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35306G, Paper&lt;/div&gt;&lt;div&gt;Yijun Jiang&lt;br/&gt;A green and effective approach for comprehensive component utilization of lignocellulosic biomass has been described, based on the hydrolysis of lignocellulosic biomass with a carbonaceous solid acid (CSA) derived 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/vrjvaspQ_vY" height="1" width="1"/&gt;</description><a10:updated>2012-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yijun Jiang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35306G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35098J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35098J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/Z0Fen_OmjBk/C2GC35098J</link><title>Eco-friendly synthesis of carbon fiber precursor polymers and their molecular characteristics</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=C2GC35098J" /&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/C2GC35098J, Paper&lt;/div&gt;&lt;div&gt;G. Santhana Krishnan, A. Burkanudeen, N. Murali, Hemant Phadnis&lt;br/&gt;A new process for the synthesis of PAC has been developed using template assisted solid phase polymerization techniques.&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/Z0Fen_OmjBk" height="1" width="1"/&gt;</description><a10:updated>2012-04-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">G. Santhana Krishnan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. Burkanudeen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">N. Murali</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hemant Phadnis</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35098J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35328H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35328H</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/F2dSyg0qogs/C2GC35328H</link><title>Microwave-assisted transition metal free reaction of aryl diazonium fluoroborate and diaryl dichalcogenides in dimethylcarbonate: A green procedure for the synthesis of unsymmetrical diaryl chalcogenides</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35328H, Paper&lt;/div&gt;&lt;div&gt;Brindaban Ranu, Debasish Kundu, Sabir Ahammed&lt;br/&gt;A convenient general and efficient procedure for the synthesis of unsymmettrical diaryl chalcogenides has been developed by the reaction of aryl diazonium fluoroborates and diaryl dichalcogenides in presence of Zinc...&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/F2dSyg0qogs" height="1" width="1"/&gt;</description><a10:updated>2012-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Brindaban Ranu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Debasish Kundu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sabir Ahammed</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35328H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35503E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35503E</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/U8HgkH9ckIs/C2GC35503E</link><title>Efficient catalytic hydrogenation of levulinic acid: a key step in biomass conversion</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35503E, Paper&lt;/div&gt;&lt;div&gt;Jozsef M Tukacs, David Kiraly, Andrea Stradi, Gyula Novodarszki, Zsuzsanna Eke, Gabor Dibo, Tamas Kegl, Laszlo T. Mika&lt;br/&gt;This is an Accepted Manuscript, which has been through the RSC Publishing peer review process and has been accepted for publication. Accepted manuscripts are published online shortly after acceptance. This version of the article will be replaced by the fully edited, formatted and proof read Advance Article as soon as this is available.&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/U8HgkH9ckIs" height="1" width="1"/&gt;</description><a10:updated>2012-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jozsef M Tukacs</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Kiraly</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrea Stradi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gyula Novodarszki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zsuzsanna Eke</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gabor Dibo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tamas Kegl</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laszlo T. Mika</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35503E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35277J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35277J</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/yKcOU6XS9qE/C2GC35277J</link><title>Catalytic procedures for multicomponent synthesis of imidazoles: selectivity control during the competitive formation of tri- and tetra-substituted imidazoles</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35277J, Paper&lt;/div&gt;&lt;div&gt;Asit Chakraborti&lt;br/&gt;The catalytic potential of different fluoroboric acid derived catalyst systems viz; aqueous fluoroboric acid, solid supported fluoroboric acid, metal tetrafluoroborates (inorganic salts), solid supported metal tetrafluoroborates, and tetraflouroborate based ionic...&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/yKcOU6XS9qE" height="1" width="1"/&gt;</description><a10:updated>2012-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Asit Chakraborti</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35277J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16378K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16378K</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/gPe7MdGmvT8/C2GC16378K</link><title>Screening of nickel catalysts for selective hydrogen production using supercritical water gasification of glucose</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=C2GC16378K" /&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/C2GC16378K, Paper&lt;/div&gt;&lt;div&gt;Pooya Azadi, Elie Afif, Faraz Azadi, Ramin Farnood&lt;br/&gt;The activity and selectivity of several heterogeneous nickel catalysts for the supercritical water gasification of biomass are reported.&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/gPe7MdGmvT8" height="1" width="1"/&gt;</description><a10:updated>2012-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Pooya Azadi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elie Afif</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Faraz Azadi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ramin Farnood</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC16378K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35147A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35147A</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/8D3vUhHGMmY/C2GC35147A</link><title>A more direct way to make catalysts: one-pot ligand-assisted aerobic stripping and electrodeposition of copper on graphite</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=C2GC35147A" /&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/C2GC35147A, Paper&lt;/div&gt;&lt;div&gt;Jose Casaban, Christopher Hardacre, Stuart L. James, M. Cristina Lagunas&lt;br/&gt;Aerobic oxidation followed by electrodeposition in one pot provides a simple and direct way to make supported catalysts with no nitrate waste.&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/~4/8D3vUhHGMmY" height="1" width="1"/&gt;</description><a10:updated>2012-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jose Casaban</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher Hardacre</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stuart L. James</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M. Cristina Lagunas</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35147A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35449G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35449G</guid><link>http://feeds.rsc.org/~r/rss/GC/~3/nlhxka13Dgs/C2GC35449G</link><title>Relationship between flash point of ionic liquids and their thermal decomposition</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Green Chem.&lt;/b&gt;&lt;/i&gt;, 2012, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2GC35449G, Paper&lt;/div&gt;&lt;div&gt;Horng-Jang Liaw, Chan-Cheng Chen, Yi-Chien Chen, Jenq-Renn Chen, Shih-Kai Huang, Sheng-Nan Liu&lt;br/&gt;Recently, ionic liquids were verified to be combustible instead of nonflammable; the contrary was thought to be true due their extremely low vapor pressure. Flash point is one of 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/nlhxka13Dgs" height="1" width="1"/&gt;</description><a10:updated>2012-04-27T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Horng-Jang Liaw</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chan-Cheng Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi-Chien Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jenq-Renn Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shih-Kai Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sheng-Nan Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/GC/C2GC35449G</feedburner:origLink></item></channel></rss>

