Please use this identifier to cite or link to this item:
Full metadata record
DC FieldValueLanguage
dc.contributor.authorJaitak, Vikas-
dc.contributor.authorKaul, V K-
dc.contributor.authorDas, Pralay-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.description.abstractA regioselective Michael reaction between aryl methyl ketones and α,β-unsaturated compounds has been carried out using basic polyionic resin as a reusable reagent. Results indicate that the reaction proceeds in consecutive manner as double Michael (27-65%) and triple Michael (40-45%) products with overall yields of 55-80%. Moreover, A-2XMP resin has also been applied on Claisen Schmidt condensations of aromatic aldehydes and ketones (acyclic as well as cyclic) under different reaction conditions yielding dehydrated products in 82-94% yield. The reactions give an opportunity for easy separation, reusability of polyionic resin and easy purification of products in continuous or multiple processing of organic compounds. en_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.52B(08) [August 2013]en_US
dc.subjectAromatic aldehydesen_US
dc.subjectAryl methyl ketonesen_US
dc.subjectClaisen-Schmidt condensationen_US
dc.subjectMichael reactionen_US
dc.titleEnviornmentally benign Michael and Claisen Schmidt reaction of aromatic carbonyl compounds by alkaline polyionic resinen_US
Appears in Collections:IJC-B Vol.52B(08) [August 2013]

Files in This Item:
File Description SizeFormat 
IJCB 52B(8) 1137-1145.pdf162.18 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.