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Reactivity of hydroxyl groups

Stacey, M. See also, Overend, W. G. Sugihara, James M., Relative Reactivities of Hydroxyl Groups of Carbohydrates, VIII, 1-44... [Pg.459]

That steric factors alone cannot account for the reactivity of hydroxyl groups was indicated by the unimolar p-toluenesulfonylation of l,4 3,6-dianhydro-D-glucitol.23 The major product, the 5-p-toluenesulfonate (45%), is derived by reaction at the sterically hindered endo-hydroxyl group, and the exo-2-p-toluenesulfonate was isolated in only 12% yield. Although the more reactive HO-5 (es-... [Pg.14]

See other pages where Reactivity of hydroxyl groups is mentioned: [Pg.94]    [Pg.242]    [Pg.460]    [Pg.13]    [Pg.15]    [Pg.17]    [Pg.19]    [Pg.21]    [Pg.23]    [Pg.23]    [Pg.25]    [Pg.26]    [Pg.27]    [Pg.29]    [Pg.29]    [Pg.31]    [Pg.33]    [Pg.35]    [Pg.37]    [Pg.38]    [Pg.39]    [Pg.41]    [Pg.43]    [Pg.43]    [Pg.45]    [Pg.47]    [Pg.49]    [Pg.51]    [Pg.53]    [Pg.55]    [Pg.57]    [Pg.59]    [Pg.61]    [Pg.61]    [Pg.63]    [Pg.63]    [Pg.65]    [Pg.67]    [Pg.69]    [Pg.71]    [Pg.73]    [Pg.75]    [Pg.77]    [Pg.79]    [Pg.81]    [Pg.83]    [Pg.85]   
See also in sourсe #XX -- [ Pg.497 ]



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