Palladium catalyzed 1, 8-conjugate addition to heptafulvene via bis-pi-allyl palladium complexes

dc.contributor.author	George, S C
dc.contributor.author	Sreeja, T
dc.contributor.author	Anas, S
dc.contributor.author	Radhakrishnan, K V
dc.contributor.author	Yamamoto, Y
dc.date.accessioned	2013-11-13T06:23:40Z
dc.date.available	2013-11-13T06:23:40Z
dc.date.issued	2011
dc.identifier.citation	Organic Letters 13(19):4984-4987;07 Oct 2011	en_US
dc.identifier.issn	1523-7060
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/737
dc.description.abstract	The palladium catalyzed 1, 8-conjugate addition of heptafulvene, an antiaromatic conjugated 8 pi-electron system, is discussed. The method is utilized for the concise synthesis of bis-functionalized cycloheptatriene (CHT) derivatives. This is the first report on the palladium catalyzed bisfunctionalization of a cyclic cross conjugated system.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Activated olefins	en_US
dc.subject	Cycloaddition reactions	en_US
dc.subject	Alpha-allylation	en_US
dc.subject	8-Cyanoheptafulvene	en_US
dc.subject	8, 8-Dicyano-3-(4'-N, N-Dimethylamino) Phenylheptafulvene	en_US
dc.subject	1, 6-Addition	en_US
dc.subject	Benzyne	en_US
dc.title	Palladium catalyzed 1, 8-conjugate addition to heptafulvene via bis-pi-allyl palladium complexes	en_US
dc.type	Article	en_US