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Issue 34, 2015
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An odorless thia-Michael addition using Bunte salts as thiol surrogates

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Abstract

A newly developed C–S bond formation process via acid-catalyzed thia-Michael addition has been demonstrated. The protocol, in which Bunte salts generated from odorless and inexpensive sodium thiosulfate and organic halides are used as the thiol precursors, provides an efficient approach for the synthesis of β-sulfido carbonyl compounds.

Graphical abstract: An odorless thia-Michael addition using Bunte salts as thiol surrogates

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Supplementary files

Article information


Submitted
23 Jan 2015
Accepted
06 Mar 2015
First published
09 Mar 2015

RSC Adv., 2015,5, 27107-27111
Article type
Paper

An odorless thia-Michael addition using Bunte salts as thiol surrogates

Y. Lin, G. Lu, C. Cai and W. Yi, RSC Adv., 2015, 5, 27107
DOI: 10.1039/C5RA01381J

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