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- W2034384029 abstract "Abstract Both enantiomers of hydroxy γ-lactones have been prepared highly enantioselectively (92–99% ee) using either AD-mix-β or AD-mix-α with both β,γ- and γ,δ-unsaturated esters. The method is exemplified by the three-step synthesis of (−) and (+)-muricatacin in 74% yield and >99% ee." @default.
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- W2034384029 date "1992-10-01" @default.
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- W2034384029 title "A general approach to γ-lactones via osmium-catalyzed asymmetric dihydroxylation. Synthesis of (−)- and (+)-muricatacin." @default.
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- W2034384029 doi "https://doi.org/10.1016/s0040-4039(00)79001-0" @default.
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