Convenient synthesis of substituted α-methylene--valerolactones in aqueous medium using Baylis-Hillman chemistry

Singh, Vijay; Batra, Sanjay

dc.contributor.author	Singh, Vijay
dc.contributor.author	Batra, Sanjay
dc.date.accessioned	2007-12-06T10:33:46Z
dc.date.available	2007-12-06T10:33:46Z
dc.date.issued	2006
dc.identifier.citation	Synthesis ( 2006), 63-72	en
dc.identifier.uri	http://hdl.handle.net/123456789/36
dc.description.abstract	A mild and convenient synthesis of substituted α-methylene--valerolactones was achieved by SN2 nucleophilic substitution of the acetates of the Baylis-Hillman adducts with acetyl acetone followed by one-pot saponification of the ester, reduction of the keto group and subsequent intramolecular ring closure in aqueous medium.	en
dc.format.extent	293915 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	(1) CDRI Communication No. 6732	en
dc.subject	Baylis-Hillman	en
dc.subject	α-methylene--valerolactone	en
dc.subject	nucleophilic substitution	en
dc.subject	aqueous medium	en
dc.title	Convenient synthesis of substituted α-methylene--valerolactones in aqueous medium using Baylis-Hillman chemistry	en
dc.type	Article	en