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Glucopyranosides alkaline hydrolysis

Madorsky and coworkers suggested that the reaction may proceed through a process similar to the formation of levoglucosan on alkaline hydrolysis of phenyl /3-D-glucopyranoside, a reaction shown to in-... [Pg.439]

Rates of the acidic hydrolysis of substituted phenyl a- and 8-mannopyranosldes showed that the a-anomers hydrolysed up to 2.7 times faster than did the 8-compounds, and up to 1.7 times faster than did the corresponding a-glucopyranosides. The work was extended to a study of the alkaline hydrolysis of these compounds and, as was to be expected, electron withdrawing groups in the aromatic rings facilitated reactions and a-compounds reacted 100-... [Pg.27]

See other pages where Glucopyranosides alkaline hydrolysis is mentioned: [Pg.236]    [Pg.110]    [Pg.70]    [Pg.61]    [Pg.13]    [Pg.16]    [Pg.194]    [Pg.64]    [Pg.1053]    [Pg.131]    [Pg.195]    [Pg.228]    [Pg.79]    [Pg.60]    [Pg.187]    [Pg.193]    [Pg.199]    [Pg.88]    [Pg.28]    [Pg.141]    [Pg.437]    [Pg.444]    [Pg.174]    [Pg.180]    [Pg.186]    [Pg.193]    [Pg.1490]    [Pg.62]    [Pg.80]    [Pg.317]    [Pg.118]    [Pg.444]    [Pg.662]    [Pg.64]    [Pg.255]    [Pg.88]    [Pg.166]   
See also in sourсe #XX -- [ Pg.46 ]



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Alkalinity, hydrolysis

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