A highly stereoselective condensation process for the conversion of carbonyl compounds to α,β-unsaturated thiol esters.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Reformatzky reactions with s-methyl-bromothioacetate
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1. An efficient access to (Z)-β-fluoroallyl alcohols based on the two carbon homologation of aromatic aldehydes by Horner–Wadsworth–Emmons reaction with 2-(diethoxyphosphinyl)-2-fluoro-ethanethioic acid, S-ethyl ester followed by reduction with sodium borohydride;Tetrahedron;2012-04
2. Synthesis of α-silylcarboxylic acids;Tetrahedron;2011-02
3. A convenient method for the synthesis of α-silylacetic acids;Tetrahedron Letters;2008-05
4. Trimethylsilylacetyl chloride;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15
5. Trimethylsilylacetic Acid;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
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