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- W2032774475 abstract "The first synthesis of (10S,12R)-10-hydroxy-12-methyl-1-oxacyclododecane-2,5-dione and its C12 epimer is reported, thereby assigning the absolute stereochemistry of the natural product. The strategy utilizes a syn selective reduction, Yamaguchi esterification, and ring-closing metathesis as the key steps." @default.
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- W2032774475 date "2008-05-01" @default.
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- W2032774475 title "The first synthesis of a 12-membered macrolide natural product via a RCM protocol: determination of absolute stereochemistry" @default.
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- W2032774475 doi "https://doi.org/10.1016/j.tetasy.2008.04.016" @default.
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