Nucleophilic heterocyclic carbene catalyzed annulation of enals to chalcones in methanol: A stereoselective synthesis of highly functionalized cyclopentanes

dc.contributor.author	Vijay Nair, G
dc.contributor.author	Beneesh, P B
dc.contributor.author	Sreekumar, V
dc.contributor.author	Vimal Varghese
dc.contributor.author	Anabha, E R
dc.contributor.author	Suresh, E
dc.date.accessioned	2013-11-20T10:01:58Z
dc.date.available	2013-11-20T10:01:58Z
dc.date.issued	2009
dc.identifier.citation	Organic Letters 11(12):2507-2510;18 Jun 2009	en_US
dc.identifier.issn	1523-7060
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/782
dc.description.abstract	Homoenolates generated from enals by nucleophilic heterocyclic carbene (NHC) catalysis undergo annulation with chalcones in methanol to afford methyl beta-hydroxycyclopentanecarboxylates, stereoselectively. Construction of four contiguous stereocenters in a stereoselective manner is noteworthy.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Gamma-Butyrolactones	en_US
dc.subject	Homoenolate reagents	en_US
dc.subject	Carbonyl compounds	en_US
dc.subject	Stetter reaction	en_US
dc.subject	Organocatalysis	en_US
dc.subject	Esters	en_US
dc.subject	Deprotonation	en_US
dc.title	Nucleophilic heterocyclic carbene catalyzed annulation of enals to chalcones in methanol: A stereoselective synthesis of highly functionalized cyclopentanes	en_US
dc.type	Article	en_US