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C-Glycosylation

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-Glycosylation 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.341 ]

See also in sourсe #XX -- [ Pg.10 , Pg.387 , Pg.429 , Pg.430 , Pg.513 , Pg.514 ]

See also in sourсe #XX -- [ Pg.177 ]

See also in sourсe #XX -- [ Pg.429 , Pg.430 , Pg.513 , Pg.514 ]

See also in sourсe #XX -- [ Pg.307 ]

See also in sourсe #XX -- [ Pg.594 ]

See also in sourсe #XX -- [ Pg.17 , Pg.20 ]




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C-Glycosyl amino acids

C-Glycosyl compounds 2,2-azobisisobutyronitrile

C-Glycosyl compounds 5-exo-trig cyclizations

C-Glycosyl compounds Barton decarboxylation

C-Glycosyl compounds N,O-protection

C-Glycosyl compounds P-bond cleavage

C-Glycosyl compounds SOMO-LUMO interactions

C-Glycosyl compounds acrylonitrile

C-Glycosyl compounds alkene reactivity

C-Glycosyl compounds alkoxyalkyl radicals

C-Glycosyl compounds allyl tin radical

C-Glycosyl compounds allylstannane

C-Glycosyl compounds anomeric effect

C-Glycosyl compounds anomeric phenyl sulfones

C-Glycosyl compounds anomeric radical

C-Glycosyl compounds cobalt method

C-Glycosyl compounds electron spin resonance

C-Glycosyl compounds fragmentation method

C-Glycosyl compounds hexopyranosyl radical

C-Glycosyl compounds hydrogen atom-transfer

C-Glycosyl compounds hydrostannylation

C-Glycosyl compounds intramolecular methods

C-Glycosyl compounds large-scale production

C-Glycosyl compounds naturally occurring

C-Glycosyl compounds one-electron reduction

C-Glycosyl compounds pentopyranosyl radical

C-Glycosyl compounds radical initiator

C-Glycosyl compounds reduction

C-Glycosyl compounds samarium diiodide

C-Glycosyl compounds stereochemistry

C-Glycosyl compounds stereoelectronic effets

C-Glycosyl compounds sugar cobalamine

C-Glycosyl compounds synthesis

C-Glycosyl compounds tertiary nitro sugar

C-Glycosyl compounds tethereD acceptors

C-Glycosyl compounds tin hydride method

C-Glycosyl compounds trialkyltin radical

C-Glycosyl compounds umpolung method

C-Glycosyl compounds unimolecular scission

C-Glycosyl compounds with linkages

C-Glycosyl derivative

C-Glycosyl phosphonates

C-Glycosyl-oxirans from acetobromoglucose

C-Glycosylation Reactions

C-Glycosylation of aromatic ring

C-Glycosylation of heterocyclic ring

C-Glycosylations

C-glycosyl compounds

C-glycosyl flavones

C-glycosyl flavonoid

C-glycosyl linkage

C«-Glycosylation procedures

Glycosyl donors with a C-2 heteroatom

Haynes, L. J., Naturally Occurring C-Glycosyl Compounds

Solution, C-glycosyl compound conformation with linkages

Stereoselective C-glycosylation

Stereoselective C-glycosylations

Synthesis of C-Glycosyl Compounds

Synthesis of C-glycosyl derivatives

Unsaturated C-glycoside from glycosyl fluoride

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