Total Synthesis of (+)-Fostriecin and (+)-Phoslactomycin B

[摘要]：(+)-Fostriecin and (+)-phoslactornycin B, which are potent and selective inhibitors of protein phosphatase, were synthesized by a highly enantio- and stereoselective approach that enabled us to prepare all possible isomers at both the C11 secondary alcohol position and the Delta(12)-double bond.

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