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- W1946388854 abstract "Enantioselective synthesis of highly potent 5-oxo-ETE receptor antagonists 5a and 6a with a high level of enantiomeric purity is described. The main feature of this work is the simple and efficient synthesis of the bi-functionalized 3-(S)-methyl-pentanedioic acid monomethyl ester (24) with the enantiomeric ratio of S/R:98.4/1.6. We investigated the asymmetric conjugate addition of MeMgBr to 5-Benzyloxy-pent-2-enoic acid methyl ester (23) catalyzed by the CuBr/(S)-Tol-BINAP system, and optimized the reaction conditions toward regioselectivity and high enantioselectivity." @default.
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- W1946388854 date "2015-12-01" @default.
- W1946388854 modified "2023-10-01" @default.
- W1946388854 title "Stereoselective synthesis of two highly potent 5-oxo-ETE receptor antagonists" @default.
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- W1946388854 doi "https://doi.org/10.1016/j.tetlet.2015.10.097" @default.
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