Title of article
Indium(I) iodide promoted cleavage of dialkyl/diaryl disulfides and subsequent anti-Markovnikov addition to styrenes: a new route to linear thioethers
Author/Authors
Ranu، نويسنده , , Brindaban C. and Mandal، نويسنده , , Tanmay، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2006
Pages
4
From page
6911
To page
6914
Abstract
The reaction of thiolate anions, generated in situ by indium(I) iodide promoted cleavage of dialkyl/diaryl disulfides, with styrenes has been investigated. Thiolate anions add to a variety of styrenes in an anti-Markovnikov manner producing linear thioethers in high yields. This method provides a new route to the synthesis of thioethers.
Keywords
Indium(I) iodide , Zinc chloride , Thioether , Anti-Markovnikov addition , styrene , Dialkyl disulfide
Journal title
Tetrahedron Letters
Serial Year
2006
Journal title
Tetrahedron Letters
Record number
1852534
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