Synthesis of highly functionalised linear pentacyclic compounds from Baylis-Hillman adduct of heteroaldehydes with azomethine ylides via [3+2] cycloaddition

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Title:	Synthesis of highly functionalised linear pentacyclic compounds from Baylis-Hillman adduct of heteroaldehydes with azomethine ylides via [3+2] cycloaddition
Authors:	Shanmugam, P Suchithra, M Baby Viswambharan Vaithiyanathan, V
Keywords:	Azomethine ylide Cycloaddition Proline Sarcosine Baylis-Hillman adduct Ninhydrin Vinyl radical cyclization Stereoselective-synthesis 1,3-dipolar cycloadditions 3-component reaction Efficient synthesis Amino-Acids L-Proline Isatin
Issue Date:	2008
Publisher:	CSIR
Citation:	Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry 47(7):1113-1116;Jul 2008
Abstract:	Montmorillonite 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.
URI:	http://ir.niist.res.in:8080/jspui/handle/123456789/2113
ISSN:	0376-4699
Appears in Collections:	2008

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