An N-heterocyclic carbene-catalyzed [8+3] annulation of tropone and enals via homoenolate

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DC Field	Value	Language
dc.contributor.author	Vijay Nair, G	-
dc.contributor.author	Manojkumar, P	-
dc.contributor.author	Sreekumar, V	-
dc.contributor.author	Suresh, E	-
dc.contributor.author	Rajasekaran, T	-
dc.date.accessioned	2014-06-17T05:48:28Z	-
dc.date.available	2014-06-17T05:48:28Z	-
dc.date.issued	2006	-
dc.identifier.citation	Journal of Organic Chemistry 71(23):8964-8965;10 Nov 2006	en_US
dc.identifier.issn	0022-3263	-
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1536	-
dc.description.abstract	A novel protocol for the annulation of tropone to enals involving nucleophilic heterocyclic carbene (NHC) catalyzed homoenolate formation has been developed. Interestingly, the reaction led to bicyclic delta-lactones instead of the expected gamma-spirolactones, presumably by the uncommon [8 + 3] annulation pathway. The strategy works well with a variety of enals.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Gamma butyrolactones	en_US
dc.subject	Alpha,beta-unsaturated aldehydes	en_US
dc.subject	Nucleophilic carbenes	en_US
dc.subject	Cycloaddition	en_US
dc.subject	Umpolung	en_US
dc.title	An N-heterocyclic carbene-catalyzed [8+3] annulation of tropone and enals via homoenolate	en_US
dc.type	Article	en_US
Appears in Collections:	2006

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