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- W2095659816 abstract "By the action of NBS in aq. DME, dl-19-bromo-20-hydroxy-DHA methyl ester 5 was prepared, which was effectively resolved by lipase PS and vinyl acetate in the presence of a thiacrown ether to give 7 and 8, each being transformed into the corresponding epoxides, 1 and 2, respectively. The absolute configuration of 8 was established by the Kusumi–Moscher method. For the purpose of biological evaluation, both epoxides were converted to the γ-lactones 3 and their 4-hydroxy derivatives 4." @default.
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- W2095659816 date "2000-03-01" @default.
- W2095659816 modified "2023-09-26" @default.
- W2095659816 title "Preparation of the enantiomers of 19-epoxy docosahexaenoic acids and their 4-hydroxy derivatives" @default.
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- W2095659816 doi "https://doi.org/10.1016/s0957-4166(00)00015-x" @default.
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