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	<channel rdf:about="http://xlink.rsc.org/jumptojournal.cfm?journal_code=GC"><title>RSC - Green Chem. latest articles</title>
		<description>RSC - Green Chem. latest articles</description>
		<link>http://xlink.rsc.org/jumptojournal.cfm?journal_code=GC</link>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
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		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
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		<prism:issn>1463-9262</prism:issn><prism:eIssn>1463-9270</prism:eIssn><prism:publisher>The Royal Society of Chemistry</prism:publisher>
		<dc:creator>The Royal Society of Chemistry</dc:creator>
		<dc:description>Royal Society of Chemistry - Green Chem. latest articles</dc:description>
		<dc:title>RSC - Green Chem. latest articles </dc:title>
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			<rdf:Seq><rdf:li rdf:resource="http://xlink.rsc.org/?DOI=b918140g&amp;RSS=1"/>
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	<item rdf:about="http://xlink.rsc.org/?DOI=b918140g&amp;RSS=1"><title>Green-light photocatalytic reduction using dye-sensitized TiO2 and transition metal nanoparticles</title>
		<link>http://xlink.rsc.org/?DOI=b918140g&amp;RSS=1</link>
		<description>Very clean green light photoreductions of nitrobenzenes are achieved by Ru(bipy)3/TiO2 photocatalysts if small amounts of transition metal salts are added, which form metal particles of a narrow size distribution under experimental conditions.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b918140g-ga.gif"/&gt;
	&lt;/p&gt;Stefan Fuldner, Ralph Mild, Heiko Ingo Siegmund, Josef A. Schroeder, Michael Gruber, Burkhard Konig &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Stefan Fuldner, Green Chem., 2010, DOI: 10.1039/b918140g&lt;br/&gt;
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		<dc:title>Green-light photocatalytic reduction using dye-sensitized TiO2 and transition metal nanoparticles</dc:title>
		<dc:creator>Stefan Fuldner</dc:creator>
		<dc:creator>Ralph Mild </dc:creator><dc:creator>Heiko Ingo Siegmund </dc:creator><dc:creator>Josef A. Schroeder </dc:creator><dc:creator>Michael Gruber </dc:creator><dc:creator>Burkhard Konig </dc:creator><dc:identifier>10.1039/b918140g</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b918140g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918140g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915681j&amp;RSS=1"><title>Environmentally benign metal-free decarboxylative aldol and Mannich reactions</title>
		<link>http://xlink.rsc.org/?DOI=b915681j&amp;RSS=1</link>
		<description>Malonic acid half esters were used as the equivalent of ester carbanions for the practical one-step synthesis of [small beta]-hydroxy and [small beta]-amino esters from aryl aldehydes and arylimines via decarboxylative aldol and Mannich type reactions. Two mechanisms were unveiled depending on the substitution of the malonyl substrate.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b915681j-ga.gif"/&gt;
	&lt;/p&gt;Jerome Baudoux, Pierre Lefebvre, Remi Legay, Marie-Claire Lasne, Jacques Rouden &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Jerome Baudoux, Green Chem., 2010, DOI: 10.1039/b915681j&lt;br/&gt;
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		<dc:title>Environmentally benign metal-free decarboxylative aldol and Mannich reactions</dc:title>
		<dc:creator>Jerome Baudoux</dc:creator>
		<dc:creator>Pierre Lefebvre </dc:creator><dc:creator>Remi Legay </dc:creator><dc:creator>Marie-Claire Lasne </dc:creator><dc:creator>Jacques Rouden </dc:creator><dc:identifier>10.1039/b915681j</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b915681j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915681j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918713h&amp;RSS=1"><title>Optimised microwave-assisted synthesis of methylcarbonate salts: a convenient methodology to prepare intermediates for ionic liquid libraries</title>
		<link>http://xlink.rsc.org/?DOI=b918713h&amp;RSS=1</link>
		<description>The synthesis of methylcarbonate salts, which have utility as clean ionic liquid precursors, has been optimised; for example, 1-butyl-1-methylpyrrolidinium methylcarbonate was obtained in 100% yield in 1 h.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b918713h-ga.gif"/&gt;
	&lt;/p&gt;John D. Holbrey, Robin D. Rogers, Saloni S. Shukla, Cecilia D. Wilfred &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
John D. Holbrey, Green Chem., 2010, DOI: 10.1039/b918713h&lt;br/&gt;
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		<dc:title>Optimised microwave-assisted synthesis of methylcarbonate salts: a convenient methodology to prepare intermediates for ionic liquid libraries</dc:title>
		<dc:creator>John D. Holbrey</dc:creator>
		<dc:creator>Robin D. Rogers </dc:creator><dc:creator>Saloni S. Shukla </dc:creator><dc:creator>Cecilia D. Wilfred </dc:creator><dc:identifier>10.1039/b918713h</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b918713h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-18</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918713h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b918176h&amp;RSS=1"><title>One-step, size-controlled synthesis of gold nanoparticles at room temperature using plant tannin</title>
		<link>http://xlink.rsc.org/?DOI=b918176h&amp;RSS=1</link>
		<description>Preparation of BT-stabilized gold nanoparticles (BT-stabilized AuNPs).</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b918176h-ga.gif"/&gt;
	&lt;/p&gt;Xin Huang, Hao Wu, Xuepin Liao, Bi Shi &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Xin Huang, Green Chem., 2010, DOI: 10.1039/b918176h&lt;br/&gt;
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		<dc:title>One-step, size-controlled synthesis of gold nanoparticles at room temperature using plant tannin</dc:title>
		<dc:creator>Xin Huang</dc:creator>
		<dc:creator>Hao Wu </dc:creator><dc:creator>Xuepin Liao </dc:creator><dc:creator>Bi Shi </dc:creator><dc:identifier>10.1039/b918176h</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b918176h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b918176h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917010c&amp;RSS=1"><title>Ligand-free iron/copper cocatalyzed N-arylations of aryl halides with amines under microwave irradiation</title>
		<link>http://xlink.rsc.org/?DOI=b917010c&amp;RSS=1</link>
		<description>Ligand-free iron/copper cocatalyzed cross-coupling reactions of aryl halides with amines were carried out efficiently, which display broad substrate scope, and are convenient, rapid, low-cost and environmentally friendly.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b917010c-ga.gif"/&gt;
	&lt;/p&gt;Diliang Guo, He Huang, Yu Zhou, Jinyi Xu, Hualiang Jiang, Kaixian Chen, Hong Liu &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Diliang Guo, Green Chem., 2010, DOI: 10.1039/b917010c&lt;br/&gt;
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		<dc:title>Ligand-free iron/copper cocatalyzed N-arylations of aryl halides with amines under microwave irradiation</dc:title>
		<dc:creator>Diliang Guo</dc:creator>
		<dc:creator>He Huang </dc:creator><dc:creator>Yu Zhou </dc:creator><dc:creator>Jinyi Xu </dc:creator><dc:creator>Hualiang Jiang </dc:creator><dc:creator>Kaixian Chen </dc:creator><dc:creator>Hong Liu </dc:creator><dc:identifier>10.1039/b917010c</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b917010c</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-11</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917010c</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913215e&amp;RSS=1"><title>Access to a primary aminosporopollenin solid support from plant spores</title>
		<link>http://xlink.rsc.org/?DOI=b913215e&amp;RSS=1</link>
		<description>Sporopollenin was converted into a primary amine form via a primary amide form, and the amine groups were further reacted.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b913215e-ga.gif"/&gt;
	&lt;/p&gt;Sylvain Barrier, Andreas Lobbert, Alia J. Boasman, Andrew N. Boa, Mark Lorch, Stephen L. Atkin, Grahame Mackenzie &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Sylvain Barrier, Green Chem., 2010, DOI: 10.1039/b913215e&lt;br/&gt;
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		<dc:title>Access to a primary aminosporopollenin solid support from plant spores</dc:title>
		<dc:creator>Sylvain Barrier</dc:creator>
		<dc:creator>Andreas Lobbert </dc:creator><dc:creator>Alia J. Boasman </dc:creator><dc:creator>Andrew N. Boa </dc:creator><dc:creator>Mark Lorch </dc:creator><dc:creator>Stephen L. Atkin </dc:creator><dc:creator>Grahame Mackenzie </dc:creator><dc:identifier>10.1039/b913215e</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b913215e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-06</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913215e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b921126h&amp;RSS=1"><title>A simple approach to reduce the environmental impact of olefin metathesis reactions: a green and renewable solvent compared to solvent-free reactions</title>
		<link>http://xlink.rsc.org/?DOI=b921126h&amp;RSS=1</link>
		<description>Olefin metathesis reactions employing an environmentally-friendly solvent, or solvent-free conditions, with low catalyst loadings have been developed.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b921126h-ga.gif"/&gt;
	&lt;/p&gt;Manuela Kniese, Michael A. R. Meier &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Manuela Kniese, Green Chem., 2010, DOI: 10.1039/b921126h&lt;br/&gt;
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		<dc:title>A simple approach to reduce the environmental impact of olefin metathesis reactions: a green and renewable solvent compared to solvent-free reactions</dc:title>
		<dc:creator>Manuela Kniese</dc:creator>
		<dc:creator>Michael A. R. Meier </dc:creator><dc:identifier>10.1039/b921126h</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b921126h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-05</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b921126h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b921203p&amp;RSS=1"><title>In vitro biocompatibility of nanoscale zerovalent iron particles (NZVI) synthesized using tea polyphenols</title>
		<link>http://xlink.rsc.org/?DOI=b921203p&amp;RSS=1</link>
		<description>A "green" protocol was developed for the rapid generation of nanoscale zerovalent iron (NZVI) particles using tea polyphenols and they were found to be nontoxic in the human keratinocyte cell (HaCaT) line.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b921203p-ga.gif"/&gt;
	&lt;/p&gt;Mallikarjuna N. Nadagouda, Alicia B. Castle, Richard C. Murdock, Saber M. Hussain, Rajender S. Varma &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Mallikarjuna N. Nadagouda, Green Chem., 2010, DOI: 10.1039/b921203p&lt;br/&gt;
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		<dc:title>In vitro biocompatibility of nanoscale zerovalent iron particles (NZVI) synthesized using tea polyphenols</dc:title>
		<dc:creator>Mallikarjuna N. Nadagouda</dc:creator>
		<dc:creator>Alicia B. Castle </dc:creator><dc:creator>Richard C. Murdock </dc:creator><dc:creator>Saber M. Hussain </dc:creator><dc:creator>Rajender S. Varma </dc:creator><dc:identifier>10.1039/b921203p</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b921203p</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-04</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b921203p</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b920195p&amp;RSS=1"><title>Exploring the possibility of using a thermostable mutant of [small beta]-glucosidase for rapid hydrolysis of quercetin glucosides in hot water</title>
		<link>http://xlink.rsc.org/?DOI=b920195p&amp;RSS=1</link>
		<description>Quercetin was produced in a rapid hydrolysis process by a thermostable [small beta]-glucosidase from a subcritical water extract of onion waste. Life cycle assessment proved the environmental benefits of this method.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b920195p-ga.gif"/&gt;
	&lt;/p&gt;Sofia Lindahl, Anna Ekman, Samiullah Khan, Christina Wennerberg, Pal Borjesson, Per J. R. Sjoberg, Eva Nordberg Karlsson, Charlotta Turner &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Sofia Lindahl, Green Chem., 2010, DOI: 10.1039/b920195p&lt;br/&gt;
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		<dc:title>Exploring the possibility of using a thermostable mutant of [small beta]-glucosidase for rapid hydrolysis of quercetin glucosides in hot water</dc:title>
		<dc:creator>Sofia Lindahl</dc:creator>
		<dc:creator>Anna Ekman </dc:creator><dc:creator>Samiullah Khan </dc:creator><dc:creator>Christina Wennerberg </dc:creator><dc:creator>Pal Borjesson </dc:creator><dc:creator>Per J. R. Sjoberg </dc:creator><dc:creator>Eva Nordberg Karlsson </dc:creator><dc:creator>Charlotta Turner </dc:creator><dc:identifier>10.1039/b920195p</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b920195p</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-04</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b920195p</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916882f&amp;RSS=1"><title>Effects of anionic structure and lithium salts addition on the dissolution of cellulose in 1-butyl-3-methylimidazolium-based ionic liquid solvent systems</title>
		<link>http://xlink.rsc.org/?DOI=b916882f&amp;RSS=1</link>
		<description>The anion structure of ILs and lithium salts added to the [C4mim][CH3COO] are found to significantly affect the solubility of the cellulose.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b916882f-ga.gif"/&gt;
	&lt;/p&gt;Airong Xu, Jianji Wang, Huiyong Wang &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Airong Xu, Green Chem., 2010, DOI: 10.1039/b916882f&lt;br/&gt;
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		<dc:title>Effects of anionic structure and lithium salts addition on the dissolution of cellulose in 1-butyl-3-methylimidazolium-based ionic liquid solvent systems</dc:title>
		<dc:creator>Airong Xu</dc:creator>
		<dc:creator>Jianji Wang </dc:creator><dc:creator>Huiyong Wang </dc:creator><dc:identifier>10.1039/b916882f</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b916882f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-04</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916882f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914628h&amp;RSS=1"><title>A facile synthesis of alkylated nitrogen heterocycles catalysed by 3D mesoporous aluminosilicates with cage type pores in aqueous medium</title>
		<link>http://xlink.rsc.org/?DOI=b914628h&amp;RSS=1</link>
		<description>A facile and efficient Friedel-Crafts alkylation of nitrogen heterocycles has been reported using mesoporous aluminosilicate AlKIT-5, with 3D cage-type pores, under environmentally benign and mild conditions in aqueous medium.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b914628h-ga.gif"/&gt;
	&lt;/p&gt;Rajashree Chakravarti, Pranjal Kalita, S. Tamil Selvan, Hamid Oveisi, V. V. Balasubramanian, M. Lakshmi Kantam, Ajayan Vinu &lt;br/&gt;
(Communication from Green Chem.)&lt;br/&gt;
Rajashree Chakravarti, Green Chem., 2010, DOI: 10.1039/b914628h&lt;br/&gt;
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		<dc:title>A facile synthesis of alkylated nitrogen heterocycles catalysed by 3D mesoporous aluminosilicates with cage type pores in aqueous medium</dc:title>
		<dc:creator>Rajashree Chakravarti</dc:creator>
		<dc:creator>Pranjal Kalita </dc:creator><dc:creator>S. Tamil Selvan </dc:creator><dc:creator>Hamid Oveisi </dc:creator><dc:creator>V. V. Balasubramanian </dc:creator><dc:creator>M. Lakshmi Kantam </dc:creator><dc:creator>Ajayan Vinu </dc:creator><dc:identifier>10.1039/b914628h</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b914628h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-04</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914628h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b917448f&amp;RSS=1"><title>An efficient approach to homocoupling of terminal alkynes: Solvent-free synthesis of 1,3-diynes using catalytic Cu(ii) and base</title>
		<link>http://xlink.rsc.org/?DOI=b917448f&amp;RSS=1</link>
		<description>An environmentally friendly, efficient method for transforming terminal acetylenes into 1,3-diynes based on catalytic amounts of a Cu(ii) salt and base under solvent-free conditions is developed; in addition, the catalyst can be recycled.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b917448f-ga.gif"/&gt;
	&lt;/p&gt;Dong Wang, Jihui Li, Na Li, Tingting Gao, Sihua Hou, Baohua Chen &lt;br/&gt;
(Communication from Green Chem.)&lt;br/&gt;
Dong Wang, Green Chem., 2010, DOI: 10.1039/b917448f&lt;br/&gt;
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		<dc:title>An efficient approach to homocoupling of terminal alkynes: Solvent-free synthesis of 1,3-diynes using catalytic Cu(ii) and base</dc:title>
		<dc:creator>Dong Wang</dc:creator>
		<dc:creator>Jihui Li </dc:creator><dc:creator>Na Li </dc:creator><dc:creator>Tingting Gao </dc:creator><dc:creator>Sihua Hou </dc:creator><dc:creator>Baohua Chen </dc:creator><dc:identifier>10.1039/b917448f</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b917448f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-30</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b917448f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915830h&amp;RSS=1"><title>Direct reduction of iron oxides based on steam reforming of bio-oil: a highly efficient approach for production of DRI from bio-oil and iron ores</title>
		<link>http://xlink.rsc.org/?DOI=b915830h&amp;RSS=1</link>
		<description>A green bio-oil-based DRI process with high efficiency, temperate operating conditions, competitive cost and real environmental benefits would be a useful route to produce DRI using renewable biomass in future.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2009/b915830h-ga.gif"/&gt;
	&lt;/p&gt;Feiyan Gong, Tongqi Ye, Lixia Yuan, Tao Kan, Youshifumi Torimoto, Mitsuo Yamamoto, Quanxin Li &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Feiyan Gong, Green Chem., 2009, DOI: 10.1039/b915830h&lt;br/&gt;
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		<dc:title>Direct reduction of iron oxides based on steam reforming of bio-oil: a highly efficient approach for production of DRI from bio-oil and iron ores</dc:title>
		<dc:creator>Feiyan Gong</dc:creator>
		<dc:creator>Tongqi Ye </dc:creator><dc:creator>Lixia Yuan </dc:creator><dc:creator>Tao Kan </dc:creator><dc:creator>Youshifumi Torimoto </dc:creator><dc:creator>Mitsuo Yamamoto </dc:creator><dc:creator>Quanxin Li </dc:creator><dc:identifier>10.1039/b915830h</dc:identifier>
		<dc:source>Green Chem., 2009, DOI: 10.1039/b915830h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-30</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915830h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916235f&amp;RSS=1"><title>Amidine-mediated delivery of CO2 from gas phase to reaction system for highly efficient synthesis of cyclic carbonates from epoxides</title>
		<link>http://xlink.rsc.org/?DOI=b916235f&amp;RSS=1</link>
		<description>A simple and energy-economic synthetic method for the efficient synthesis of cyclic carbonates under ambient conditions (1 atm, rt to 45 [degree]C) is reported by insertion of CO2 (g) into the corresponding epoxides by using a catalytic amount of reversible CO2 fixation-release system MTHP.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b916235f-ga.gif"/&gt;
	&lt;/p&gt;Balaka Barkakaty, Kazuhide Morino, Atsushi Sudo, Takeshi Endo &lt;br/&gt;
(Communication from Green Chem.)&lt;br/&gt;
Balaka Barkakaty, Green Chem., 2010, DOI: 10.1039/b916235f&lt;br/&gt;
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		<dc:title>Amidine-mediated delivery of CO2 from gas phase to reaction system for highly efficient synthesis of cyclic carbonates from epoxides</dc:title>
		<dc:creator>Balaka Barkakaty</dc:creator>
		<dc:creator>Kazuhide Morino </dc:creator><dc:creator>Atsushi Sudo </dc:creator><dc:creator>Takeshi Endo </dc:creator><dc:identifier>10.1039/b916235f</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b916235f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-29</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916235f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916825g&amp;RSS=1"><title>High performance magnetic separation of gold nanoparticles for catalytic oxidation of alcohols</title>
		<link>http://xlink.rsc.org/?DOI=b916825g&amp;RSS=1</link>
		<description>We here present the preparation of magnetically recoverable supported gold nanoparticles. The magnetic separation approach facilitates the recovery of gold nanoparticles for catalytic oxidation of alcohols.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b916825g-ga.gif"/&gt;
	&lt;/p&gt;Rafael L. Oliveira, Pedro K. Kiyohara, Liane M. Rossi &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Rafael L. Oliveira, Green Chem., 2010, DOI: 10.1039/b916825g&lt;br/&gt;
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		<dc:title>High performance magnetic separation of gold nanoparticles for catalytic oxidation of alcohols</dc:title>
		<dc:creator>Rafael L. Oliveira</dc:creator>
		<dc:creator>Pedro K. Kiyohara </dc:creator><dc:creator>Liane M. Rossi </dc:creator><dc:identifier>10.1039/b916825g</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b916825g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-29</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916825g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b915465e&amp;RSS=1"><title>Perfluoro-tagged, phosphine-free palladium nanoparticles supported on silica gel: application to alkynylation of aryl halides, Suzuki-Miyaura cross-coupling, and Heck reactions under aerobic conditions</title>
		<link>http://xlink.rsc.org/?DOI=b915465e&amp;RSS=1</link>
		<description>Perfluoro-tagged palladium nanoparticles immobilized on fluorous silica gel are efficient and reusable catalysts for the alkynylation of aryl halides, the Suzuki-Miyaura cross-coupling, as well as the Heck reaction.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b915465e-ga.gif"/&gt;
	&lt;/p&gt;Roberta Bernini, Sandro Cacchi, Giancarlo Fabrizi, Giovanni Forte, Francesco Petrucci, Alessandro Prastaro, Sandra Niembro, Alexandr Shafir, Adelina Vallribera &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Roberta Bernini, Green Chem., 2010, DOI: 10.1039/b915465e&lt;br/&gt;
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		<dc:title>Perfluoro-tagged, phosphine-free palladium nanoparticles supported on silica gel: application to alkynylation of aryl halides, Suzuki-Miyaura cross-coupling, and Heck reactions under aerobic conditions</dc:title>
		<dc:creator>Roberta Bernini</dc:creator>
		<dc:creator>Sandro Cacchi </dc:creator><dc:creator>Giancarlo Fabrizi </dc:creator><dc:creator>Giovanni Forte </dc:creator><dc:creator>Francesco Petrucci </dc:creator><dc:creator>Alessandro Prastaro </dc:creator><dc:creator>Sandra Niembro </dc:creator><dc:creator>Alexandr Shafir </dc:creator><dc:creator>Adelina Vallribera </dc:creator><dc:identifier>10.1039/b915465e</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b915465e</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-29</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b915465e</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919806g&amp;RSS=1"><title>A quantum-chemical-based guide to analyze/quantify the cytotoxicity of ionic liquids</title>
		<link>http://xlink.rsc.org/?DOI=b919806g&amp;RSS=1</link>
		<description>The Quantitative Structure-Activity Map (QSAM), a new concept developed here, was proposed as a quantum-chemical-based guide to analyze/quantify the cytotoxicity of ionic liquids, including the non-linear mixture effects of the toxicophores constituting the IL structure.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b919806g-ga.gif"/&gt;
	&lt;/p&gt;J. S. Torrecilla, J. Palomar, J. Lemus, F. Rodriguez &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
J. S. Torrecilla, Green Chem., 2010, DOI: 10.1039/b919806g&lt;br/&gt;
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		<dc:title>A quantum-chemical-based guide to analyze/quantify the cytotoxicity of ionic liquids</dc:title>
		<dc:creator>J. S. Torrecilla</dc:creator>
		<dc:creator>J. Palomar </dc:creator><dc:creator>J. Lemus </dc:creator><dc:creator>F. Rodriguez </dc:creator><dc:identifier>10.1039/b919806g</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b919806g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-28</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919806g</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914774h&amp;RSS=1"><title>Ruthenium-catalyzed synthesis of [small beta]-oxo esters in aqueous medium: Scope and limitations</title>
		<link>http://xlink.rsc.org/?DOI=b914774h&amp;RSS=1</link>
		<description>Selective synthesis of [small beta]-oxo esters, by addition of carboxylic acids to terminal propargylic alcohols, can be efficiently performed in water using hydrosoluble ruthenium(II) catalysts.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b914774h-ga.gif"/&gt;
	&lt;/p&gt;Victorio Cadierno, Javier Francos, Jose Gimeno &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Victorio Cadierno, Green Chem., 2010, DOI: 10.1039/b914774h&lt;br/&gt;
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		<dc:title>Ruthenium-catalyzed synthesis of [small beta]-oxo esters in aqueous medium: Scope and limitations</dc:title>
		<dc:creator>Victorio Cadierno</dc:creator>
		<dc:creator>Javier Francos </dc:creator><dc:creator>Jose Gimeno </dc:creator><dc:identifier>10.1039/b914774h</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b914774h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-28</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914774h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919807p&amp;RSS=1"><title>A highly efficient Cu/La2O3 catalyst for transfer dehydrogenation of primary aliphatic alcohols</title>
		<link>http://xlink.rsc.org/?DOI=b919807p&amp;RSS=1</link>
		<description>La2O3-supported Cu nanoparticles are highly active for transfer dehydrogenation of primary aliphatic alcohols to aldehydes. When used for 1-octanol, the yield of 1-octanal can be as high as 63%.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b919807p-ga.gif"/&gt;
	&lt;/p&gt;Ruijuan Shi, Fei Wang, Tana, Yong Li, Xiumin Huang, Wenjie Shen &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Ruijuan Shi, Green Chem., 2010, DOI: 10.1039/b919807p&lt;br/&gt;
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		<dc:title>A highly efficient Cu/La2O3 catalyst for transfer dehydrogenation of primary aliphatic alcohols</dc:title>
		<dc:creator>Ruijuan Shi</dc:creator>
		<dc:creator>Fei Wang </dc:creator><dc:creator>Tana </dc:creator><dc:creator>Yong Li </dc:creator><dc:creator>Xiumin Huang </dc:creator><dc:creator>Wenjie Shen </dc:creator><dc:identifier>10.1039/b919807p</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b919807p</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-27</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919807p</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916042f&amp;RSS=1"><title>Aerobic oxidative carboxylation of olefins with metalloporphyrin catalysts</title>
		<link>http://xlink.rsc.org/?DOI=b916042f&amp;RSS=1</link>
		<description>Dioxoruthenium porphyrin and tetrabutylammonium iodide were discovered as efficient catalyst systems for a three component reaction of olefin, O2, and CO2 at ambient temperature under low pressure.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b916042f-ga.gif"/&gt;
	&lt;/p&gt;Dongsheng Bai, Huanwang Jing &lt;br/&gt;
(Communication from Green Chem.)&lt;br/&gt;
Dongsheng Bai, Green Chem., 2010, DOI: 10.1039/b916042f&lt;br/&gt;
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		<dc:title>Aerobic oxidative carboxylation of olefins with metalloporphyrin catalysts</dc:title>
		<dc:creator>Dongsheng Bai</dc:creator>
		<dc:creator>Huanwang Jing </dc:creator><dc:identifier>10.1039/b916042f</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b916042f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-27</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916042f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b916852d&amp;RSS=1"><title>Highly efficient synthesis of thioesters in water</title>
		<link>http://xlink.rsc.org/?DOI=b916852d&amp;RSS=1</link>
		<description>Diverse thioesters were efficiently prepared via the reaction of tertiary thioamides with alkyl halides in the presence of catalytic amounts of NaI, hexadecyltrimethylammonium bromide (HTAB), and DABCO in water.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2009/b916852d-ga.gif"/&gt;
	&lt;/p&gt;Hassan Zali Boeini, Maryam Eshghi Kashan &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Hassan Zali Boeini, Green Chem., 2009, DOI: 10.1039/b916852d&lt;br/&gt;
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		<dc:title>Highly efficient synthesis of thioesters in water</dc:title>
		<dc:creator>Hassan Zali Boeini</dc:creator>
		<dc:creator>Maryam Eshghi Kashan </dc:creator><dc:identifier>10.1039/b916852d</dc:identifier>
		<dc:source>Green Chem., 2009, DOI: 10.1039/b916852d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-27</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b916852d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b914726h&amp;RSS=1"><title>Photooxygenation of furans in water and ionic liquid solutions</title>
		<link>http://xlink.rsc.org/?DOI=b914726h&amp;RSS=1</link>
		<description>The photooxygenation of various substituted furans in water and in ionic liquids proceeds selectively and leads to products in good yields depending mainly on the solvent polarity and/or nucleophilicity.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2009/b914726h-ga.gif"/&gt;
	&lt;/p&gt;Anna Astarita, Flavio Cermola, Marina DellaGreca, Maria Rosaria Iesce, Lucio Previtera, Maria Rubino &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Anna Astarita, Green Chem., 2009, DOI: 10.1039/b914726h&lt;br/&gt;
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		<dc:title>Photooxygenation of furans in water and ionic liquid solutions</dc:title>
		<dc:creator>Anna Astarita</dc:creator>
		<dc:creator>Flavio Cermola </dc:creator><dc:creator>Marina DellaGreca </dc:creator><dc:creator>Maria Rosaria Iesce </dc:creator><dc:creator>Lucio Previtera </dc:creator><dc:creator>Maria Rubino </dc:creator><dc:identifier>10.1039/b914726h</dc:identifier>
		<dc:source>Green Chem., 2009, DOI: 10.1039/b914726h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-27</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b914726h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b913398d&amp;RSS=1"><title>Catalyst-free silylation of alcohols and phenols by promoting HMDS in CH3NO2 as solvent</title>
		<link>http://xlink.rsc.org/?DOI=b913398d&amp;RSS=1</link>
		<description>A novel and efficient uncatalyzed method for the silylation of alcohols and phenols is developed. A variety of aromatic and aliphatic alcohols as well as phenols undergo the silylation in very short reaction time with excellent yield.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b913398d-ga.gif"/&gt;
	&lt;/p&gt;Santosh T. Kadam, Sung Soo Kim &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Santosh T. Kadam, Green Chem., 2010, DOI: 10.1039/b913398d&lt;br/&gt;
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		<dc:title>Catalyst-free silylation of alcohols and phenols by promoting HMDS in CH3NO2 as solvent</dc:title>
		<dc:creator>Santosh T. Kadam</dc:creator>
		<dc:creator>Sung Soo Kim </dc:creator><dc:identifier>10.1039/b913398d</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b913398d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-26</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b913398d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b919660a&amp;RSS=1"><title>New one-pot multistep process with multifunctional catalysts: decreasing the E factor in the synthesis of fine chemicals</title>
		<link>http://xlink.rsc.org/?DOI=b919660a&amp;RSS=1</link>
		<description>A series of fine chemicals has been synthesized in one pot using multifunctional base-acid-metal catalysts. The E factor is decreased by one order of magnitude with respect to the conventional routes.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/GC/2010/b919660a-ga.gif"/&gt;
	&lt;/p&gt;Maria J. Climent, Avelino Corma, Sara Iborra, Maria Mifsud, Alexandra Velty &lt;br/&gt;
(Paper from Green Chem.)&lt;br/&gt;
Maria J. Climent, Green Chem., 2010, DOI: 10.1039/b919660a&lt;br/&gt;
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		<dc:title>New one-pot multistep process with multifunctional catalysts: decreasing the E factor in the synthesis of fine chemicals</dc:title>
		<dc:creator>Maria J. Climent</dc:creator>
		<dc:creator>Avelino Corma </dc:creator><dc:creator>Sara Iborra </dc:creator><dc:creator>Maria Mifsud </dc:creator><dc:creator>Alexandra Velty </dc:creator><dc:identifier>10.1039/b919660a</dc:identifier>
		<dc:source>Green Chem., 2010, DOI: 10.1039/b919660a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-26</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b919660a</dc:identifier>
	</item>
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