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- W2085884893 abstract "The compound 2 comprises a southern-half subunit of the fungicidal macrolide soraphen A 1. It was prepared by a Meinwald reaction of the enolate of S-7 with the lactone S-8. Its enantiomer and diastereomers were synthesized in a similar manner. The lactone S-8 and its enantiomer R-8 were prepared by three different routes, including the enantioselective catalytic reduction of the β-keto ester 17. These lactones are new and potentially useful as C-5 asymmetric building blocks." @default.
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- W2085884893 date "1995-03-01" @default.
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- W2085884893 title "The enantioselective synthesis of simplified southern-half fragments of soraphen A" @default.
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- W2085884893 doi "https://doi.org/10.1016/0040-4020(95)00098-s" @default.
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