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- W1969997208 abstract "Abstract An enantioselective synthesis of the trideoxy sugar 4-O- acetyl- l -rhodinopyranose ( 7 ) is described. A key feature of the synthetic strategy is a Sharpless asymmetric dihydroxylation followed by a lipase-mediated mono-esterification of the resultant diol ( 3→4→6 )." @default.
- W1969997208 created "2016-06-24" @default.
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- W1969997208 date "2010-08-17" @default.
- W1969997208 modified "2023-09-26" @default.
- W1969997208 title "ChemInform Abstract: Synthesis of 4-O-Acetyl-L-rhodinopyranose via a Tandem Sharpless Asymmetric Dihydroxylation/Lipase-Catalyzed Transesterification." @default.
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- W1969997208 doi "https://doi.org/10.1002/chin.199539237" @default.
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