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Rearrangement with saccharides

VII. Rearrangement of Saccharides with Other Lewis Acids. 192... [Pg.127]

Laboratory synthesis of P-substituted monosaccharides has been carried out (6.853) and (6.854). Interactions between saccharides and phosphonates have been studied and various derivatives isolated [15]. Aminoethylphosphonic acid reacts readily with d-glucose, for example, and undergoes rearrangement to give an aminoketose [16]. [Pg.1013]

In a novel approach to rare saccharides, cyclohexanones such as 63, accessible from Fertia rearrangements, could be manipulated as indicated in Scheme 10 similar chemistry could be carried out with 0-4 (cyclohexanone numbering) linked via a glycosidic bond to another sugar unit, to give a disaccharide analogue of 64. ... [Pg.191]

See other pages where Rearrangement with saccharides is mentioned: [Pg.147]    [Pg.338]    [Pg.411]    [Pg.288]    [Pg.69]    [Pg.235]    [Pg.87]    [Pg.433]    [Pg.192]    [Pg.196]    [Pg.381]    [Pg.357]    [Pg.49]    [Pg.397]    [Pg.142]    [Pg.178]    [Pg.187]    [Pg.719]    [Pg.231]    [Pg.704]    [Pg.58]    [Pg.49]    [Pg.20]    [Pg.322]    [Pg.20]    [Pg.322]   
See also in sourсe #XX -- [ Pg.44 ]



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