Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21287
Title: Nickel chloride hexahydrate: A novel reagent for Michael addition on α,β-unsaturated acids — A facile one-step route to 3-arylmercaptopropionic acids from thiophenols and α,β-unsaturated acids
Authors: Gogia, Santosh
Sirohi, Reenu
Gupta, Suman
Kishore, D
Joshi, B C
Issue Date: May-2004
Publisher: NISCAIR-CSIR, India
IPC Code: Int.Cl.7 C 07 G 53/00
Abstract: Michael additions have been successfully carried out in presence of a base, but when an α,β-unsaturated acid is a substrate, it would be most unlikely for a carboxylate ion bearing α,β-unsaturated site to undergo a Michael addition. This problem has been circumvented in the present paper by carrying out a nickel chloride hexahydrate mediated Michael addition of thiophenols 1a-k on acrylic acid and on cinnamic acid to give 3-aryl mercaptopropionic acids 3a-k in excellent yield.
Page(s): 1008-1011
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.43B(05) [May 2004]

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