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Glucosan and derivs

These various possibilities for oxidation-resistant 1,2-diols demonstrate the need for caution in the interpretation of the results of periodate and lead tetraacetate oxidation. As in the studies of D-glucosan < 1,4 > 0-< 1,6> and D-galactosana, supporting evidence based on other chemical reactions and the formation of derivatives should be obtained for the choice between absence of adjacent hydroxyl groups and presence of resistant 1,2-diols. [Pg.52]

D-Glucosan (1,5)/3(1,6) and its 3-methyl derivative are believed to form low rotating complexes involving the hydroxyl groups on carbon atoms 2 and 4. Approximate calculations of the 02—04 distance indicates that such complexing might be expected provided the pyranoside... [Pg.129]


See other pages where Glucosan and derivs is mentioned: [Pg.725]    [Pg.455]    [Pg.457]    [Pg.725]    [Pg.456]    [Pg.458]    [Pg.725]    [Pg.455]    [Pg.457]    [Pg.725]    [Pg.456]    [Pg.458]    [Pg.40]    [Pg.356]    [Pg.227]    [Pg.189]    [Pg.207]    [Pg.463]    [Pg.14]    [Pg.192]    [Pg.176]    [Pg.39]    [Pg.462]    [Pg.377]    [Pg.463]    [Pg.89]    [Pg.228]    [Pg.91]    [Pg.250]    [Pg.527]   
See also in sourсe #XX -- [ Pg.6 , Pg.83 ]




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Glucosan

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