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- W218959220 abstract "Publisher Summary This chapter discusses the C-4 substitution of methyl d -glucosides and malto-oligosaccharides. Malto-oligosaccharides substituted at only one hydroxyl group of the nonreducing end-unit were prepared by a sequence of reactions, namely, perbenzylation of amylose to give tri- O -benzylamylose, methanolysis of tri- O -benzylamylose to give benzylated methyl malto-oligosaccharides having only the hydroxyl group at C-4 of the nonreducing end-unit unsubstituted, reaction at the unsubstituted hydroxyl group, and debenzylation to give methyl malto-oligosaccharides substituted only at C-4 of the nonreducing terminus. The method is a general one and can be used with other polysaccharides to give products modified—in the nonreducing terminus—at the hydroxyl group that was originally involved in the glycosidic linkage." @default.
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- W218959220 date "1972-01-01" @default.
- W218959220 modified "2023-10-16" @default.
- W218959220 title "C-4 Substitution of Methyl d-Glucosides and Malto-oligosaccharides" @default.
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- W218959220 doi "https://doi.org/10.1016/b978-0-12-746206-6.50076-x" @default.
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