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

Gogia, Santosh; Sirohi, Reenu; Gupta, Suman; Kishore, D; Joshi, B C

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Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21287

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DC Field	Value	Language
dc.contributor.author	Gogia, Santosh	-
dc.contributor.author	Sirohi, Reenu	-
dc.contributor.author	Gupta, Suman	-
dc.contributor.author	Kishore, D	-
dc.contributor.author	Joshi, B C	-
dc.date.accessioned	2013-09-20T10:51:25Z	-
dc.date.available	2013-09-20T10:51:25Z	-
dc.date.issued	2004-05	-
dc.identifier.issn	0975-0983(Online); 0376-4699(Print)	-
dc.identifier.uri	http://hdl.handle.net/123456789/21287	-
dc.description	1008-1011	en_US
dc.description.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.	en_US
dc.language.iso	en_US	en_US
dc.publisher	NISCAIR-CSIR, India	en_US
dc.relation.ispartofseries	Int.Cl.⁷ C 07 G 53/00	en_US
dc.rights	CC Attribution-Noncommercial-No Derivative Works 2.5 India	en_US
dc.source	IJC-B Vol.43B(05) [May 2004]	en_US
dc.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	en_US
dc.type	Article	en_US
Appears in Collections:	IJC-B Vol.43B(05) [May 2004]

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