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- W1991911730 abstract "The diphenol 1 was resolved into its antipodes and their absolute configuration was established. The levorotatory isomer R-(−)-1 was oxidized to the dienone R-(−)-6, which was rearranged to afford natural (−)-multifloramine (R-(−)-7), thus establishing that the latter has the R-configuration. By the same reaction sequences, the enantiomeric diphenol S-(+)-1 was transformed to provide (+)-multifloramine (S-(+)-7) of the S-configuration." @default.
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- W1991911730 date "1969-01-01" @default.
- W1991911730 modified "2023-09-24" @default.
- W1991911730 title "Totalsynthese und absolute Konfiguration von natürlichem Multifloramin" @default.
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- W1991911730 doi "https://doi.org/10.1002/hlca.19690520316" @default.
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