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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/36

Title: Convenient synthesis of substituted α-methylene--valerolactones in aqueous medium using Baylis-Hillman chemistry
Authors: Singh, Vijay
Batra, Sanjay
Keywords: Baylis-Hillman
α-methylene--valerolactone
nucleophilic substitution
aqueous medium
Issue Date: 2006
Citation: Synthesis ( 2006), 63-72
Series/Report no.: (1) CDRI Communication No. 6732
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.
URI: http://hdl.handle.net/123456789/36
Appears in Collections:Medicinal and Process Chemistry

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