Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/822
Title: Palladium catalyzed tandem ring opening-ring closing reaction of diazabicyclic alkenes: A facile one pot strategy for cyclopentannulation of heterocycles
Authors: Jubi John
Indu, U
Suresh, E
Radhakrishnan, K V
Keywords: Bicyclic hydrazines
Functionilized cyclopentenes
Stereoselective synthesis
Cyclopentadiene
Prostacyclin
Arylation
Enantioselective desymmetrization
Issue Date: 2009
Publisher: American Chemical Society
Citation: Journal of the American Chemical Society 131(14):5042-5043;15 Apr 2009
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
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/822
ISSN: 0002-7863
Appears in Collections:2009

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