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<title>Chiral Ureas and Thioureas Supported on Polystyrene for Enantioselective Aza-Henry Reaction in Solvent-free conditions</title>
<creator>Pedrosa Sáez, Rafael</creator>
<creator>Andrés García, José María</creator>
<creator>Ávila, Deisy P.</creator>
<creator>Ceballos, Miriam</creator>
<creator>Pindado Hernández, Rodrigo</creator>
<subject>Catalizadores</subject>
<subject>Química orgánica</subject>
<description>Producción Científica</description>
<description>Novel bifunctional ureas and thioureas inmovilized on sulfonylpystyrene have been prepared as recoverable and reusable organocatalysts and used in the stereoselective aza-Henry reaction under solvent-free conditions. The activity and stereoselection of the catalysts are dependent on the length of the tether bringing the active site and the polymer, being the catalyst derived from 1,6-hexane diamine the best one. It has been also demonstrated that the supported catalysts are more effective than the homologous soluble catalysts.</description>
<date>2016-12-05</date>
<date>2016-12-05</date>
<date>2015</date>
<type>info:eu-repo/semantics/article</type>
<identifier>Green Chemistry, 2015, vol.17, p. 2217-2225</identifier>
<identifier>1463-9262</identifier>
<identifier>http://uvadoc.uva.es/handle/10324/21447</identifier>
<identifier>10.1039/C4GC02474E</identifier>
<identifier>2217</identifier>
<identifier>17</identifier>
<identifier>2225</identifier>
<identifier>Green Chemistry</identifier>
<language>eng</language>
<relation>http://pubs.rsc.org/</relation>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</rights>
<rights>Attribution-NonCommercial-NoDerivatives 4.0 International</rights>
<publisher>Royal Society of Chemistry</publisher>
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