Palladium catalyzed tandem ring opening-ring closing reaction of diazabicyclic alkenes: A facile one pot strategy for cyclopentannulation of heterocycles

dc.contributor.author	Jubi John
dc.contributor.author	Indu, U
dc.contributor.author	Suresh, E
dc.contributor.author	Radhakrishnan, K V
dc.date.accessioned	2013-11-22T09:31:01Z
dc.date.available	2013-11-22T09:31:01Z
dc.date.issued	2009
dc.identifier.citation	Journal of the American Chemical Society 131(14):5042-5043;15 Apr 2009	en_US
dc.identifier.issn	0002-7863
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/822
dc.description.abstract	A novel palladium catalyzed protocol for the synthesis of cyclopentene fused heterocycles from diazabicyclic alkenes and ortho-functionalized aryliodides has been elaborated. The reaction can be tuned toward the formation of either 3,4-disubstituted cyclopentenes or cyclopentene fused heterocycles by careful manipulation of the reaction parameters. A number of cyclopentene fused benzofurans and indole derivatives were prepared in excellent yield by utilizing the developed methodology	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Bicyclic hydrazines	en_US
dc.subject	Functionilized cyclopentenes	en_US
dc.subject	Stereoselective synthesis	en_US
dc.subject	Cyclopentadiene	en_US
dc.subject	Prostacyclin	en_US
dc.subject	Arylation	en_US
dc.subject	Enantioselective desymmetrization	en_US
dc.title	Palladium catalyzed tandem ring opening-ring closing reaction of diazabicyclic alkenes: A facile one pot strategy for cyclopentannulation of heterocycles	en_US
dc.type	Article	en_US