<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fan, X. Y.</style></author><author><style face="normal" font="default" size="100%">Alza, E.</style></author><author><style face="normal" font="default" size="100%">Pericas, M. A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A highly active organocatalyst for the asymmetric alpha-aminoxylation of aldehydes and alpha-hydroxylation of ketones</style></title><secondary-title><style face="normal" font="default" size="100%">RSC AdvancesRSC Advances</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Rsc Adv</style></alt-title><short-title><style face="normal" font="default" size="100%">RSC Adv.</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">aldol</style></keyword><keyword><style  face="normal" font="default" size="100%">amino-acid</style></keyword><keyword><style  face="normal" font="default" size="100%">aminocatalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">carbonyl-compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">catalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">chemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">derivatives</style></keyword><keyword><style  face="normal" font="default" size="100%">mannich</style></keyword><keyword><style  face="normal" font="default" size="100%">proline</style></keyword><keyword><style  face="normal" font="default" size="100%">sulfonamide</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><number><style face="normal" font="default" size="100%">15</style></number><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">6164-6166</style></pages><isbn><style face="normal" font="default" size="100%">2046-2069</style></isbn><language><style face="normal" font="default" size="100%">English</style></language><abstract><style face="normal" font="default" size="100%">Enantiopure trans-3-trifluoromethylsulfonylamino-4-silyloxypyrrolidines efficiently catalyse the asymmetric alpha-aminoxylation of aldehydes. At 1% catalyst loading (solvent-free conditions) or at 2% catalyst loading (acetonitrile solution) aldehydes are completely converted in short reaction times leading to alpha-aminoxylation products with very high (96-99%) enantioselectivity.</style></abstract><accession-num><style face="normal" font="default" size="100%">WOS:000306216600008</style></accession-num><notes><style face="normal" font="default" size="100%">971PPTimes Cited:3Cited References Count:36</style></notes><auth-address><style face="normal" font="default" size="100%">Inst Chem Res Catalonia ICIQ, Tarragona 43007, SpainUniv Barcelona, Dept Quim Organ, E-08028 Barcelona, Spain</style></auth-address></record></records></xml>