Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/822
Full metadata record
DC FieldValueLanguage
dc.contributor.authorJubi John-
dc.contributor.authorIndu, U-
dc.contributor.authorSuresh, E-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2013-11-22T09:31:01Z-
dc.date.available2013-11-22T09:31:01Z-
dc.date.issued2009-
dc.identifier.citationJournal of the American Chemical Society 131(14):5042-5043;15 Apr 2009en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/822-
dc.description.abstractA 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 methodologyen_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectBicyclic hydrazinesen_US
dc.subjectFunctionilized cyclopentenesen_US
dc.subjectStereoselective synthesisen_US
dc.subjectCyclopentadieneen_US
dc.subjectProstacyclinen_US
dc.subjectArylationen_US
dc.subjectEnantioselective desymmetrizationen_US
dc.titlePalladium catalyzed tandem ring opening-ring closing reaction of diazabicyclic alkenes: A facile one pot strategy for cyclopentannulation of heterocyclesen_US
dc.typeArticleen_US
Appears in Collections:2009

Files in This Item:
File Description SizeFormat 
2009 _ 00068.pdf
  Restricted Access
111.3 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.