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Chiral azabicyclo-N-oxyls mediated enantioselective electrooxidation of sec-alcohols


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Title: Chiral azabicyclo-N-oxyls mediated enantioselective electrooxidation of sec-alcohols
Authors: Shiigi, Hirofumi / Mori, Hiroyuki / Tanaka, Tomoaki / Demizu, Yosuke / Onomura, Osamu
Issue Date: 1-Sep-2008
Publisher: Elsevier
Citation: Tetrahedron Letters, 49(36), pp.5247-5251; 2008
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
URI: http://hdl.handle.net/10069/18792
ISSN: 00404039
DOI: 10.1016/j.tetlet.2008.06.112
Rights: Copyright (c) 2008 Elsevier Ltd All rights reserved.
Type: Journal Article
Text Version: author
Appears in Collections:Articles in academic journal

Citable URI : http://hdl.handle.net/10069/18792

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