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Enantioselective epoxidation by an optically active hydroperoxide
Authors:Hans-Jü  rgen Hamann,Eugen H  ft,Marek Chmielewski,Sylvester Maciejewski
Affiliation:Hans-Jürgen Hamann,Eugen Höft,Marek Chmielewski,Sylvester Maciejewski
Abstract:Enantioselective epoxidation of prochiral allylic alcohols with optically active 4,6-di-O-acetyl-2,3-dideoxy-α-D -threo-hex-2-enopyranosyl hydroperoxide in the presence of Ti(O-i-Pr)4 gives chiral epoxy alcohols with moderate enantiomeric excess. © 1993 Wiley-Liss, Inc.
Keywords:asymmetric induction  capillary gas chromatography  cyclodextrin stationary phases
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