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- W2080387356 abstract "The enantioselective total synthesis of idesolide has been accomplished in 20% overall yield from a known allylic alcohol by a nine-step sequence involving the Sharpless asymmetric epoxidation as the source of chirality and an efficient NaHCO3-promoted dimerization of the monomeric form of idesolide as the key transformation." @default.
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- W2080387356 date "2010-07-01" @default.
- W2080387356 modified "2023-09-25" @default.
- W2080387356 title "Enantioselective total synthesis of idesolide via NaHCO3-promoted dimerization" @default.
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- W2080387356 doi "https://doi.org/10.1016/j.tet.2010.05.034" @default.
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