Title of article
Product selectivity in the electroreduction of thioesters
Author/Authors
M. Weïwer، نويسنده , , S. Olivero، نويسنده , , E. Du?ach، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
6
From page
1709
To page
1714
Abstract
The electroreduction of differently substituted aromatic and aliphatic thioesters (RCOSR′) led to regioselective reactions depending on the nature of the substituents. Thus, the cleavage between the carbonyl group and the SR′ group afforded α-diketones and the cleavage between the RCOS group and the alkyl R′ group afforded thiocarboxylic acids selectively.
Keywords
thioesters , Thioacids , ?-Diketone , Electroreductive homocoupling
Journal title
Tetrahedron
Serial Year
2005
Journal title
Tetrahedron
Record number
1088397
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