Sequential combination of Michael and acetalization reactions: Direct catalytic asymmetric synthesis of functionalized 4-nitromethyl-chromans as drug intermediates

dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Sakthidevi, Rajasekar
dc.date.accessioned 2022-03-27T09:40:45Z
dc.date.available 2022-03-27T09:40:45Z
dc.date.issued 2010-10-07
dc.description.abstract Functionalized chiral 4-nitromethyl-chromans as drug intermediates were achieved for the first time through sequential combination of Michael and acetalization reactions on 2-(2-nitro-vinyl)-phenols with acetone and alcohols in the presence of a catalytic amount of 9-amino-9-deoxyepiquinine and Ph 2CHCO2H followed by p-TSA. © 2010 The Royal Society of Chemistry.
dc.identifier.citation Organic and Biomolecular Chemistry. v.8(19)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c0ob00189a
dc.identifier.uri http://xlink.rsc.org/?DOI=c0ob00189a
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13188
dc.title Sequential combination of Michael and acetalization reactions: Direct catalytic asymmetric synthesis of functionalized 4-nitromethyl-chromans as drug intermediates
dc.type Journal. Article
dspace.entity.type
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