NHC-catalysed annulation of enals to tethered dienones: efficient synthesis of bicyclic dienes

dc.contributor.author	Vijay Nair, G
dc.contributor.author	Sreekumar, V
dc.contributor.author	Bineesh, P B
dc.contributor.author	Vimal Varghese
dc.contributor.author	Paul, R R
dc.contributor.author	Suresh, E
dc.date.accessioned	2014-05-22T10:13:54Z
dc.date.available	2014-05-22T10:13:54Z
dc.date.issued	2010
dc.identifier.citation	Organic & Biomolecular Chemistry 8(21):4861-4866;24 Aug 2010	en_US
dc.identifier.issn	1477-0520
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1439
dc.description.abstract	Homoenolates generated from alpha,beta-unsaturated aldehydes using NHC catalysis underwent facile addition to dibenzylidene cyclohexanone to afford bicyclic cyclopentenes as single diastereomers.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	N-heterocyclic carbenes	en_US
dc.subject	Gamma-butyrolactones	en_US
dc.subject	Multicomponent reactions	en_US
dc.subject	Stereoselective-synthesis	en_US
dc.subject	Stetter reaction	en_US
dc.subject	Conjugate umpolung	en_US
dc.subject	Aldehydes	en_US
dc.subject	Homoenolate	en_US
dc.subject	chalcones	en_US
dc.title	NHC-catalysed annulation of enals to tethered dienones: efficient synthesis of bicyclic dienes	en_US
dc.type	Article	en_US