N‑Heterocyclic Carbene Catalyzed Reaction of Cinnamils Leading to the Formation of 2,3,8-Triaryl Vinyl Fulvenes: An Uncommon Transformation

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DC Field	Value	Language
dc.contributor.author	Sinu, C R	-
dc.contributor.author	Eringathodi, Suresh	-
dc.contributor.author	Vijay Nair	-
dc.date.accessioned	2016-12-30T06:00:37Z	-
dc.date.available	2016-12-30T06:00:37Z	-
dc.date.issued	2012-02-12	-
dc.identifier.citation	ORGANIC LETTERS ;2013 Vol. 15, No. 24 6230–6233	en_US
dc.identifier.uri	http://hdl.handle.net/123456789/2609	-
dc.description.abstract	In the general context of organocatalysis,1 N-heterocyclic carbenes (NHCs) occupy a prominent position. NHC catalysis2 originated as early as 1958 with Breslow’s demonstration3 that thiazolylidene was involved in the thiazolium catalyzed benzoin condensation.4 However, with the exception of its application in benzoin condensation 5 and the Stetter reaction,6 NHC catalysis received little attention for a long time. A significant change in this situation occurred in 2004, when Glorius7 and Bode8	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	An unexpected transformation	en_US
dc.subject	6-diarylhexa-1	en_US
dc.subject	5-diene-3,4-diones (cinnamils) to 2,3,8-triaryl vinyl fulvenes via N-Heterocyclic Carbene (NHC) catalysis is reported	en_US
dc.title	N‑Heterocyclic Carbene Catalyzed Reaction of Cinnamils Leading to the Formation of 2,3,8-Triaryl Vinyl Fulvenes: An Uncommon Transformation	en_US
dc.type	Article	en_US
Appears in Collections:	2013

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