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• W2949520022 abstract "Various anomerically pure isopropenyl α- and β-glycopyranosides have been synthesized and shown to undergo synthetically useful transglycosylation reactions with a variety of primary and secondary carbohydrate alcohols. Although stable when stored, isopropenyl glycosides are readily activated as glycosyl donors by a variety of electrophiles, including N-iodosuccinimide/triflic acid, trimethylsilyl triflate, and triflic anhydride. Under conditions that retard formation of the glycosyl cation, the reactivity of isopropenyl glycosides is diverted away from transglycosylation and toward electrophilic addition across the vinyl ether double bond." @default.
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• W2949520022 date "1996-01-01" @default.
• W2949520022 modified "2023-10-11" @default.
• W2949520022 title "The Chemistry of Isopropenyl Glycopyranosides. Transglycosylations and Other Reactions" @default.
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• W2949520022 doi "https://doi.org/10.1021/jo960190p" @default.
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