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• W1986088064 abstract "An efficient route to two 3-O-acyl-2-deoxy-4,6-O-isopropylidene-2-trichloroacetamido-d-glucopyranosyl trichloroacetimidate donors is reported. As demonstrated for the 3-O-acetyl derivative, these building blocks are exquisite β-d-glucosamine donors when reacted either with simple alcohols or with complex oligosaccharides. Besides, their protection pattern is compatible with selective deprotection and subsequent chain elongation at O-3 of the newly incorporated glucosamine residue." @default.
• W1986088064 created "2016-06-24" @default.
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• W1986088064 date "2008-09-01" @default.
• W1986088064 modified "2023-10-16" @default.
• W1986088064 title "Efficient route to orthogonally protected precursors of 2-acylamino-2-deoxy-3-O-substituted-β-d-glucopyranose derivatives and use thereof" @default.
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• W1986088064 doi "https://doi.org/10.1016/j.tetlet.2008.06.052" @default.
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