| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274378 | Tetrahedron Letters | 2008 | 5 Pages |
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).
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hirofumi Shiigi, Hiroyuki Mori, Tomoaki Tanaka, Yosuke Demizu, Osamu Onomura,