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C-aryl glucosides

C-aryl glucosides, structure, 86/ 94/ C-aryl mannosides, structure, 85/ synthesis... [Pg.179]

This classification still left out many monomeric ellagitannins the structures of many of which result from chemical transformations other than those strictly mediated by oxidative processes. In this vein, some important structural modifications have to do with the opening of the o-glucopyranose core, the formation of C-aryl glucosidic bonds, and condensation reactions taking place at the glucose C-1 locus. As these ellagitannins still... [Pg.84]

Pissarra, J., Louren o, S., Gonzalez-Paramas, A.M., Mateus, N., Santos-Buelga, C., Silva, A.M.S., De Freitas, V. (2004). Structural characterization of new malvidin-3-glucoside-catechin aryl/alkyl pigments. J. Agric. Food Chem. 52, 5519-5526. [Pg.460]

Pissarra J, Lourenco S, Gonzales-Paramas AM, Mateus N, Santos-Buelga C, Silva AMS, De Freitas V (2004) Stmctural characterization of new malvidin 3-glucoside-catechin aryl/ alkyl-linked pigments. J Agric Food Chem 52 5519-5526... [Pg.2008]

See other pages where C-aryl glucosides is mentioned: [Pg.83]    [Pg.86]    [Pg.83]    [Pg.86]    [Pg.331]    [Pg.81]    [Pg.85]    [Pg.1490]    [Pg.124]    [Pg.336]    [Pg.47]    [Pg.136]    [Pg.172]    [Pg.287]    [Pg.47]    [Pg.52]    [Pg.83]    [Pg.28]    [Pg.66]    [Pg.896]    [Pg.311]    [Pg.293]    [Pg.102]    [Pg.493]    [Pg.169]    [Pg.490]    [Pg.497]    [Pg.498]    [Pg.33]    [Pg.84]    [Pg.140]    [Pg.935]    [Pg.296]    [Pg.47]    [Pg.493]    [Pg.110]    [Pg.20]    [Pg.43]    [Pg.43]    [Pg.200]    [Pg.180]    [Pg.85]    [Pg.45]    [Pg.95]   
See also in sourсe #XX -- [ Pg.86 , Pg.94 ]



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