Synthesis of novel functionalized 3-spiropyrrolizidine and 3-spiropyrrolidine oxindoles from Baylis-Hillman adducts of isatin and heteroaldehydes with azomethine ylides via [3+2]- cycloaddition

dc.contributor.author	Shanmugam, P
dc.contributor.author	Baby Viswambharan
dc.contributor.author	Suchithra, M
dc.date.accessioned	2011-03-15T11:18:46Z
dc.date.available	2011-03-15T11:18:46Z
dc.date.issued	2007-10-11
dc.identifier.citation	Organic Letters 9(21):4095-4098;11 Oct 2007	en_US
dc.identifier.other	145-2007
dc.identifier.uri	http://hdl.handle.net/123456789/65
dc.description.abstract	A novel regioselective synthesis of a number of functionalized 3-spiropyrrolizidine and 3-spiropyrrolidine oxindoles from Baylis-Hillman adducts of isatin and heteroaldehydes via [3+2] cycloaddition of azomethine ylides in excellent yields has been reported.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society, USA	en_US
dc.title	Synthesis of novel functionalized 3-spiropyrrolizidine and 3-spiropyrrolidine oxindoles from Baylis-Hillman adducts of isatin and heteroaldehydes with azomethine ylides via [3+2]- cycloaddition	en_US
dc.type	Article	en_US