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Glycuronic acids preparation

Several electrochemical oxidations have also been described for preparing glycuronic acids. A nickel hydroxide electrode in alkaline solution has been particularly useful because of its selectivity, as secondary alcohols... [Pg.218]

Bromine (hypobromite) and hypoiodite oxidations are particularly useful for the preparation of aldonic acids from aldoses and of aldaric acids from glycuronic acids. Primary alcohol groups also undergo oxidation by these reagents, although this conversion is of less value glycosides can thus be converted into glycosiduronic acids, and alditols into aldoses and aldonic acids. [Pg.313]

The literature on /3-D-glucosiduronic acids is particularly voluminous, and the subject has been extensively reviewed from several aspects. Section III, dealing with this class of compounds, is devoted more to a general overview of their preparation, characterization, and reactions than to individual members. On the other hand, the categories of 1-esters of glycuronic acids and of (glycosylamine)uronic acids, which appear not to have been treated previously as separate topics, receive relatively more attention. [Pg.58]


See other pages where Glycuronic acids preparation is mentioned: [Pg.374]    [Pg.3]    [Pg.4]    [Pg.218]    [Pg.220]    [Pg.223]    [Pg.233]    [Pg.260]    [Pg.268]    [Pg.126]    [Pg.176]    [Pg.351]    [Pg.155]    [Pg.298]   
See also in sourсe #XX -- [ Pg.216 , Pg.217 , Pg.218 , Pg.219 , Pg.220 ]




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Glycuronic acids

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