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- W2997942623 abstract "An efficient α‐sialylation methodology for various primary, secondary, and tertiary alcohol acceptors has been developed. The sialic acid ethyl thioglycoside 1b , bearing a 4‐nitropicoloyl moiety as the stereodirecting group at the C4 position, was utilized as the glycosyl donor, and the sialylation reaction was activated with N ‐iodosuccinimide and catalytic triflic acid in a 1:1 mixture of dichloromethane/acetonitrile as solvent. The method was successfully applied to the stereocontrolled synthesis of protected trisaccharide 11 found in the repeating unit of serotype Ia Group B Streptococcus capsular polysaccharide." @default.
- W2997942623 created "2020-01-10" @default.
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- W2997942623 date "2020-01-27" @default.
- W2997942623 modified "2023-09-27" @default.
- W2997942623 title "A Highly α-Stereoselective Sialylation Method Using 4-<i>O</i> -4-Nitropicoloyl Thiosialoside Donor" @default.
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- W2997942623 doi "https://doi.org/10.1002/ejoc.201901587" @default.
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