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- W2177386985 abstract "An asymmetric synthesis of the C10C24 fragment of the potent antitumor macrolide, peloruside A is described. All three stereogenic centers have been enantioselectively constructed utilizing Evans alkylation, Brown asymmetric allylboration, and a substrate controlled epoxide formation. Other key reactions involved Grubbs's ring-closing olefin metathesis and Ando's Z-selective olefination reaction." @default.
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- W2177386985 date "2003-10-01" @default.
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- W2177386985 title "Synthetic studies of microtubule stabilizing agent peloruside A: an asymmetric synthesis of C10C24 segment" @default.
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- W2177386985 doi "https://doi.org/10.1016/j.tetlet.2003.08.023" @default.
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