<?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%">Kulkarni, M. A.</style></author><author><style face="normal" font="default" size="100%">Pandurangi, V. R.</style></author><author><style face="normal" font="default" size="100%">Desai, Uday V.</style></author><author><style face="normal" font="default" size="100%">Wadgaonkar, P. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Practical and highly efficient protocol for multicomponent synthesis of beta-phosphonomalononitriles and 2-amino-4H-chromen-4-yl phosphonates using diethylamine as a novel organocatalyst</style></title><secondary-title><style face="normal" font="default" size="100%">Comptes Rendus Chimie</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">2-amino-4H-chromenes</style></keyword><keyword><style  face="normal" font="default" size="100%">beta-phosphonomalononitriles</style></keyword><keyword><style  face="normal" font="default" size="100%">diethylamine</style></keyword><keyword><style  face="normal" font="default" size="100%">multicomponent reactions</style></keyword><keyword><style  face="normal" font="default" size="100%">organocatalyst</style></keyword><keyword><style  face="normal" font="default" size="100%">Phospha-Michael reaction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">SEP</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">9</style></number><publisher><style face="normal" font="default" size="100%">ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER</style></publisher><pub-location><style face="normal" font="default" size="100%">23 RUE LINOIS, 75724 PARIS, FRANCE</style></pub-location><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">745-752</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Diethylamine has been demonstrated for the first time to be a highly efficient organocatalyst in the solvent-free synthesis of beta-phosphonomalononitriles by a three component condensation of aldehyde, malononitrile and dialkyl phosphite at ambient temperature. The applicability of the same catalyst in the synthesis of diethyl (2-amino-3-cyano-chromene-4-yl) phosphonic acid esters has also been described. (c) 2012 Published by Elsevier Masson SAS on behalf of Academie des sciences.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">9</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">1.98</style></custom4></record><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%">Kupwade, R. V.</style></author><author><style face="normal" font="default" size="100%">Khot, S. S.</style></author><author><style face="normal" font="default" size="100%">Lad, U. P.</style></author><author><style face="normal" font="default" size="100%">Desai, U. V.</style></author><author><style face="normal" font="default" size="100%">Wadgaonkar, P. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Catalyst-free oxidation of sulfides to sulfoxides and diethylamine catalyzed oxidation of sulfides to sulfones using oxone as an oxidant</style></title><secondary-title><style face="normal" font="default" size="100%">Research on Chemical Intermediates</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">diethylamine</style></keyword><keyword><style  face="normal" font="default" size="100%">organocatalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxone</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulfones</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulfoxides</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">DEC</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">43</style></volume><pages><style face="normal" font="default" size="100%">6875-6888</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;We describe here our journey from the failure of our attempts in controlled oxidation of sulfides to sulfoxides using an Oxone(A (R))-KBr combination to our success in the development of a catalyst-free protocol for the oxidation of sulfides to sulfoxides using Oxone as an oxidant. We also describe the failure of our attempts at the oxidation of sulfides to sulfones using an excess of Oxone-KBr as well as Oxone, and our success towards the development of a rapid, scalable and chromatography-free protocol for the oxidation of sulfides to sulfones using diethylamine-Oxone as an unprecedented catalyst-oxidant combination. [GRAPHICS] .&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">12</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">1.674</style></custom4></record></records></xml>