Novel nucleophilic heterocyclic carbene mediated stereoselective conjugate addition of enals to nitrostyrenes via homoenolate

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DC Field	Value	Language
dc.contributor.author	Vijay Nair, G	-
dc.contributor.author	Sinu, C R	-
dc.contributor.author	Beneesh, P B	-
dc.contributor.author	Varghese, V	-
dc.contributor.author	Anu Jose	-
dc.contributor.author	Suresh, E	-
dc.date.accessioned	2014-03-28T05:51:04Z	-
dc.date.available	2014-03-28T05:51:04Z	-
dc.date.issued	2009	-
dc.identifier.citation	Organic Letters 11(24):5570-5573;17 Dec 2009	en_US
dc.identifier.issn	1523-7060	-
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1240	-
dc.description.abstract	A stereoselective Michael addition of homoenolate, generated from enals by nucleophilic heterocyclic carbene (NHC) catalysis, to beta-nitrostyrenes is reported for the first time. The products of this reaction obtained in good yields are of potential value in the synthesis of a variety of acyclic and heterocyclic compounds.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Bond forming reactions	en_US
dc.subject	Gamma butyrolactones	en_US
dc.subject	Michael additions	en_US
dc.subject	Enantioselective synthesis	en_US
dc.subject	Carbonyl compounds	en_US
dc.subject	Silyl ether	en_US
dc.subject	Nitroalkenes	en_US
dc.title	Novel nucleophilic heterocyclic carbene mediated stereoselective conjugate addition of enals to nitrostyrenes via homoenolate	en_US
dc.type	Article	en_US
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