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Sugar glycosylation

Acid-catalyzed, Anomerization of O-Acylated Derivatives of Sugars, Glycosyl Halides,... [Pg.21]

Hydroxyproline and hydroxylysine occur most noticeably in collagen. These are formed by modification of proline and lysine residues by specific enzymes after synthesis of the collagen chains. It is interesting to note that proly/hydroxylase, which hydroxylates proline, requires ascorbate (vitamin C) as a coreactant. Other chemical modifications known to occur commonly are the attachment of sugars (glycosylation) to asparagine, serine, and threonine residues and the phosphorylation of serine. Chemical modifications are also associated with the transport of proteins out of the cells in which they are synthesized. [Pg.505]

In order to preserve the cyclic form of the sugar, glycosyl derivatives of 2-hydroxyacetaldehyde (192) have been proposed as precursors of thiosemicarbazone ligands343 (193, Scheme 60). The corresponding cop-per(II) and manganese(II) complexes exhibited superoxide dismutase mimetic activity, with IC50 values ranging from 0.2 to 0.8 fiM. [Pg.101]

Trichloroacetonitrile reacts with glycosidic hydroxy groups of protected sugars to form glycosyl trichloroacetimidates (R. R. Schmidt, 1980, 1984,1985,1986 B. Wegmann, 1988). The imidate is substituted by alcohols in the presence of trimethylsilyl trifluoromethanesulfonate... [Pg.270]

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]


See other pages where Sugar glycosylation is mentioned: [Pg.202]    [Pg.37]    [Pg.145]    [Pg.102]    [Pg.290]    [Pg.18]    [Pg.277]    [Pg.15]    [Pg.233]    [Pg.747]    [Pg.127]    [Pg.279]    [Pg.132]    [Pg.35]    [Pg.133]    [Pg.126]    [Pg.133]    [Pg.84]    [Pg.74]    [Pg.136]    [Pg.202]    [Pg.37]    [Pg.145]    [Pg.102]    [Pg.290]    [Pg.18]    [Pg.277]    [Pg.15]    [Pg.233]    [Pg.747]    [Pg.127]    [Pg.279]    [Pg.132]    [Pg.35]    [Pg.133]    [Pg.126]    [Pg.133]    [Pg.84]    [Pg.74]    [Pg.136]    [Pg.268]    [Pg.270]    [Pg.272]    [Pg.330]    [Pg.295]    [Pg.250]    [Pg.537]    [Pg.127]    [Pg.133]    [Pg.284]    [Pg.476]    [Pg.477]    [Pg.478]    [Pg.479]    [Pg.484]    [Pg.289]    [Pg.80]    [Pg.1014]    [Pg.227]    [Pg.284]    [Pg.368]    [Pg.829]    [Pg.7]    [Pg.31]    [Pg.49]   
See also in sourсe #XX -- [ Pg.150 , Pg.151 ]




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Anhydro Sugars as Glycosyl Donors

C-Glycosyl compounds sugar cobalamine

C-Glycosyl compounds tertiary nitro sugar

Free Sugars as Glycosyl Donors

Glycosyl donors 1,2-anhydro sugars

Glycosyl fluorides sugars

Glycosylation 1-hydroxy sugars

Glycosylation Methods Alkylations of Reducing Sugars

Glycosylation nucleotide sugars

Glycosylation sugar carbonates

Recycling of Sugar Nucleotides in Enzymatic Glycosylation

Special Problems in Glycosylation Reactions 2-Deoxy Sugars

Sugars glycosyl donors

Unprotected sugars Fischer glycosylation

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