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• W2010843655 startingPage "1096" @default.
• W2010843655 abstract "Competitive glycosylation experiments with a galactofuranosyl trichloroacetimidate donor were performed with glucosamine acceptors having a free 4-OH group and carrying different protecting groups at N-2, O-3, and O-6. The most reactive acceptor is the N-dimethylmaleimido 3,6-di-O-benzylated derivative (6c), which reacts even faster than the oxazolidinone 1a. Molecular orbital calculations have helped to rationalize these experimental facts in terms of a hard–hard reaction occurring between the donor and the acceptor." @default.
• W2010843655 created "2016-06-24" @default.
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• W2010843655 date "2006-07-01" @default.
• W2010843655 modified "2023-10-14" @default.
• W2010843655 title "A comparative study of the influence of some protecting groups on the reactivity of d-glucosamine acceptors with a galactofuranosyl donor" @default.
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• W2010843655 doi "https://doi.org/10.1016/j.carres.2006.03.030" @default.
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