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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2121
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dc.contributor.authorAnas, S-
dc.contributor.authorSajisha, V S-
dc.contributor.authorJubi John-
dc.contributor.authorNayana Joseph, J-
dc.contributor.authorSholly, C G-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2016-01-18T07:07:57Z-
dc.date.available2016-01-18T07:07:57Z-
dc.date.issued2008-
dc.identifier.citationTetrahedron 64(41):9689-9697;06 Oct 2008en_US
dc.identifier.issn0040-4020-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/2121-
dc.description.abstractA facile synthesis of substituted alkylidene cyclopentenes through a palladium catalyzed ring opening of fulvene derived bicyclic hydrazines with various organometallic reagents is described. The products are versatile synthons with multiple points for functionalization and can be used in the synthesis of a number of biologically active molecules.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPentafulvenesen_US
dc.subjectAlkylidene cyclopentenesen_US
dc.subjectFulveneen_US
dc.subjectPalladiumen_US
dc.subjectBicyclic hydrazinesen_US
dc.subjectEnantioselective total-synthesisen_US
dc.subjectFischer carbene complexesen_US
dc.subjectLinearly fused tricyclopentanoidsen_US
dc.subjectCycloadditionen_US
dc.subjectFunctionalized cyclopentenesen_US
dc.subjectStereoselective-synthesisen_US
dc.subjectOrganoindium reagentsen_US
dc.subjectEfficient synthesisen_US
dc.subjectAsymmetric-synthesisen_US
dc.subject3-oxidopyrylium betaineen_US
dc.titleFacile synthesis of alkylidene cyclopentenes via palladium catalyzed ring opening of fulvene derived bicyclic hydrazinesen_US
dc.typeArticleen_US
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