Abstract
AbstractCopper(I) catalyzed Grignard reaction of compound (II) and cyclohexene oxide (I) yields the racemic trans‐alcohol (III) which is separated by enantioselective saponification of its acetate (IV) using commercially avaible PLAP (pig liver acetone powder), producing pure enantiomeres (‐)‐(III) and (+)‐(III).
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