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C-Glycosylations

The naturally occurring C-nucleosides containing C-glycosyl linkages are shown in Table 1. [Pg.118]

C-Glycosyl compounds have a carbon atom ia place of the exocycHc oxygen atom of the acetal group and, therefore, are branched cycHc ethers. An example is the naturally occurring anthroquiaone dye, carminic acid [1260-17-9] (Cl Natural Red 4). [Pg.478]

Two- and three-component Hantzsch reactions using C-glycosylated reagents have been reported as an alternate method for conducting asymmetric syntheses of 1,4-dihydropyridines." ° Reaction of 109, 110 and 97 generate 111 with Ri = sugar. Alternatively, 112 and 113 produce 111 with Ri = sugar. While the yields were acceptable (60-90%), the diastereomeric ratio varied from 30-60%. [Pg.318]

Dondoni has elaborated this methodology to include C-glycosylated dihydro-pyrimidines/ The sugar residue can be a subunit in the aldehyde, 1,3-dicarbonyl, or urea consequently, substitution of the DHPM ring may occur in one of three places depending on which component originally contains the glycosidic residue. In the example... [Pg.516]

Fischer projection of acyclic form, 56-57 glycosides, 132-135 C-glycosyl compounds, 139-140 N-glycosyl derivatives, 137-139 glycosyl halides, 136-137 glycosyl residues, 125 isotopic substitution and isotopic labelling, 91 me so forms, 59 optical rotation, 59 parent structure choice, 53... [Pg.487]

C-Glycosyl derivatives may be prepared by utilizing glycosyl fluorides. Ishido and coworkers reported that the reaction of 2,3,5-tri-O-benzyl-a-(36a) or - -D-ribofuranosyl fluoride (36fi) with isopropenyl trimethylsilyl ether under BF3 catalysis (0.1 -0.05 mol. equiv. for the fluoride, in ether or acetonitrile) gave a mixture of 4,7-anhydro-5,6,8-tri-C)-benzyl-l,3-dideoxy-D-altro- (139, major) and -D-a//o-2-octulose (140) 139 was stated to isomerized to 140 (should be vice versa) under Lewis acid catalysis. Similar... [Pg.116]

The anion of nitromethane adds easily to the carbonyl functions of sugars. This is a useful strategy for extension of the carbon chain.100 2-Acetamido-2-deoxy-P-D-glucose (A-acetyl-D-glucosamine) is the carbohydrate unit of glycoproteins that occurs most often. The nitromethy-lation method provides a straightforward route to a series of C-glycosyl compounds with the acetamido functionality (Eq. 3.62).101... [Pg.49]

Scheme 10. C-Glycosylation of aromatic alcohols with olivoses and olivosides in the presence of Montmorillonite K-10. Scheme 10. C-Glycosylation of aromatic alcohols with olivoses and olivosides in the presence of Montmorillonite K-10.

See other pages where C-Glycosylations is mentioned: [Pg.329]    [Pg.49]    [Pg.509]    [Pg.510]    [Pg.510]    [Pg.512]    [Pg.514]    [Pg.519]    [Pg.519]    [Pg.789]    [Pg.793]    [Pg.46]    [Pg.139]    [Pg.485]    [Pg.488]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.118]    [Pg.119]    [Pg.10]    [Pg.87]    [Pg.198]    [Pg.219]    [Pg.276]    [Pg.296]    [Pg.213]    [Pg.213]    [Pg.559]    [Pg.560]    [Pg.95]    [Pg.40]    [Pg.41]    [Pg.42]    [Pg.44]    [Pg.45]    [Pg.45]    [Pg.49]    [Pg.91]   
See also in sourсe #XX -- [ Pg.74 ]




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C-Glycosylation

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