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dc.contributor.authorShanmugam, P-
dc.contributor.authorSuchithra, M-
dc.contributor.authorBaby Viswambharan-
dc.contributor.authorVaithiyanathan, V-
dc.date.accessioned2016-01-18T07:03:55Z-
dc.date.available2016-01-18T07:03:55Z-
dc.date.issued2008-
dc.identifier.citationIndian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry 47(7):1113-1116;Jul 2008en_US
dc.identifier.issn0376-4699-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/2113-
dc.description.abstractMontmorillonite K10 clay promoted one-pot synthesis of penta- and tetracyclic systems from Baylis-Hillman adduct of heteroaldehydes with azomethine ylides generated from ninhydrin and proline or sarcosine via [3+2] cycloaddition is reported.en_US
dc.language.isoenen_US
dc.publisherCSIRen_US
dc.subjectAzomethine ylideen_US
dc.subjectCycloadditionen_US
dc.subjectProlineen_US
dc.subjectSarcosineen_US
dc.subjectBaylis-Hillman adducten_US
dc.subjectNinhydrinen_US
dc.subjectVinyl radical cyclizationen_US
dc.subjectStereoselective-synthesisen_US
dc.subject1,3-dipolar cycloadditionsen_US
dc.subject3-component reactionen_US
dc.subjectEfficient synthesisen_US
dc.subjectAmino-Acidsen_US
dc.subjectL-Prolineen_US
dc.subjectIsatinen_US
dc.titleSynthesis of highly functionalised linear pentacyclic compounds from Baylis-Hillman adduct of heteroaldehydes with azomethine ylides via [3+2] cycloadditionen_US
dc.typeArticleen_US
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