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Synthesis 2009(17): 2935-2953
DOI: 10.1055/s-0029-1216930
DOI: 10.1055/s-0029-1216930
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Total Synthesis of (+)-Fostriecin and (+)-Phoslactomycin B
Further Information
Received
29 May 2009
Publication Date:
07 August 2009 (online)
Publication History
Publication Date:
07 August 2009 (online)
Abstract
(+)-Fostriecin and (+)-phoslactomycin 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 Δ¹²-double bond.
Key words
antibiotics - fostriecin - phoslactomycin - total synthesis
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