Title of article
Convenient enantioselective synthesis of new 1,4-sulfanylalcohols from γ-lactones
Author/Authors
Filippi، نويسنده , , Jean-Jacques and Fernandez، نويسنده , , Xavier and Lizzani-Cuvelier، نويسنده , , Louisette and Loiseau، نويسنده , , Andre Michel، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
4
From page
6267
To page
6270
Abstract
A synthetic strategy based upon three basic reactions—enzymatic resolution, oxygen–sulfur exchange, reduction—allowed us to carry out an easy and useful synthesis of a series of new 1,4-sulfanylalcohols from aliphatic γ-lactones. Final products have been obtained in good yields with enantiomeric excesses in a 66–91% range.
Keywords
1 , 4-sulfanylalcohols , enzymatic resolution , Reduction , thionation reaction , ?-Lactones
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1653457
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