Title of article
Chiral azabicyclo-N-oxyls mediated enantioselective electrooxidation of sec-alcohols
Author/Authors
Shiigi، نويسنده , , Hirofumi and Mori، نويسنده , , Hiroyuki and Tanaka، نويسنده , , Tomoaki and Demizu، نويسنده , , Yosuke and Onomura، نويسنده , , Osamu، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2008
Pages
5
From page
5247
To page
5251
Abstract
Enantiomerically pure azabicyclo-N-oxyls were prepared from l-hydroxyproline. They mediated enantioselective electrooxidation of racemic sec-alcohols to afford optically active sec-alcohols with moderate to high s value (up to 21).
Keywords
Chiral nitroxyl radical , enantioselective oxidation , Optically active alcohol , Electrooxidation
Journal title
Tetrahedron Letters
Serial Year
2008
Journal title
Tetrahedron Letters
Record number
1860735
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