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Enantioselective Allylic Oxidation of Olefins Using Chiral Quinolinyl‐oxazoline Copper Complex Catalysts
Author(s) -
Li ZhiPeng,
Wu XinYan,
Zhou QiLin,
Chan WingLai
Publication year - 2001
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.20010190107
Subject(s) - chemistry , allylic rearrangement , oxazoline , enantioselective synthesis , catalysis , copper , enantiomer , acetone , organic chemistry , medicinal chemistry , enantiomeric excess
Copper complexes of chiral quinolinyl‐oxazoline have been studied as the catalysts for enantioselective allylic oxidation of cycloalkenes with tert ‐butyl perbenzoate. Using 5 mol% of these chiral catalysts, optical active allylic benzoates were obtained in moderate enantiomeric excesses. CuOTf prepared in situ , CuClO 4 and CuPF 6 were found to be good precatalysts in acetone.
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