Chemoenzymatic enantioselective synthesis of 7-azabicyclo[2.2.1]heptane derivatives

Tetrahedron: Asymmetry(2011)

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摘要
The enantioselective acylation (desymmetrization) of meso-7-azabicyclo[2.2.1]heptanediol 2 by vinyl acetate in the presence of Candida antarctica lipase B gave the corresponding (1R,2R,3S,4S)-monoester 4 in high enantiomeric purity (ee⩾98%).
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