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Oligosaccharides unsaturated

The dipping unit can also be employed to impregnate adsorbent layers. It is easy in this way to produce tungstate- [127] or silver nitrate-impregnated layers for separating oligosaccharides or unsaturated compounds. [Pg.86]

As impressive as the oligosaccharide domain is, calicheamici-none, the aglycon sector 7 (see Scheme 3) is the most striking substructure of calicheamicin y. The rigid bicyclic framework of 7 accommodates an unusual allylic methyl trisulfide and a novel pattern of unsaturation that had not been encountered in natural products before. [Pg.527]

All oligosaccharides containing this group (5) at their nonreducing end will be termed unsaturated. ... [Pg.355]

Carbohydrates Ceiiuiose Starch 1 Hemiceiiuiose Lignin J ( monosaccharides "j ( hexoses "j Cx(H20)y < oligosaccharides > pentoses > [ chitin J ( glucosamine J (C2H20)4 unsaturated aromatic alcohols —> polyhydroxy carboxylic aoids HPOy, GO2, CH4, glucose, fructose, galactose, arabinose, ribose, xylose... [Pg.625]

Eur. J. Biochem. (1980) 111, 295-298 Nomenclature of unsaturated monosaccharides Eur. J. Biochem. (1981) 119, 1-3 Nomenclature of branched-chain monosaccharides Eur. J. Biochem. (1981) 119, 5-8 Abbreviated terminology of oligosaccharide chains /. Biol Chem. (1982) 257, 3347-3351 Polysaccharide nomenclature /. Biol Chem. (1982) 257, 3352-3354 Symbols for specifying the conformation of polysaccharide chains... [Pg.83]

Compounds 1-10. c-x " c-x represent 05 and Cl of cyclic and acyclic carbohydrate, respectively, in which the carbohydrate moiety may be any mono or oligosaccharide, a or ano-mer (cyclic forms) C Hjn+, is a saturated aliphatic chain, while alkyl maybe either a saturated or an unsaturated aliphatic chain... [Pg.283]

XXXVI. The Nature of the Unsaturated Residue in Some Oligosaccharides Produced by the Action of Sodium Hydroxide-Sodium Borohydride on Blood Group A, B, and H Substances, Carbohydrate Res. (1967) 4,165. [Pg.367]

The IUPAC-IUBMB short form symbolism18 2-Carb-38.5 is used here and elsewhere in this chapter for designation of oligosaccharide structures. Parent monosaccharide residues are the d enantiomers except for IdoA, which is the l enantiomer. Uronic acid residues modified by 44-unsaturation are prefixed by A4tS, and the associated anomeric symbol relates to the configuration at the 5-position of that residue before 4,5-elimination. The abbreviation HexA is used to denote either d-G1cA or L-IdoA. [Pg.202]

See other pages where Oligosaccharides unsaturated is mentioned: [Pg.525]    [Pg.527]    [Pg.88]    [Pg.785]    [Pg.785]    [Pg.78]    [Pg.103]    [Pg.4]    [Pg.40]    [Pg.65]    [Pg.457]    [Pg.291]    [Pg.189]    [Pg.212]    [Pg.1155]    [Pg.191]    [Pg.192]    [Pg.199]    [Pg.200]    [Pg.204]    [Pg.205]    [Pg.210]    [Pg.211]    [Pg.211]    [Pg.244]    [Pg.321]    [Pg.105]    [Pg.208]    [Pg.186]    [Pg.234]    [Pg.49]    [Pg.60]    [Pg.29]    [Pg.542]    [Pg.604]   
See also in sourсe #XX -- [ Pg.24 , Pg.253 ]

See also in sourсe #XX -- [ Pg.253 ]



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Oligosaccharides unsaturated, synthesis

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