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D-Monosaccharides

The designations D and L refer to the configuration of the stereocenter farthest from the aldehyde or ketone group on a monosaccharide chain. When the monosaccharide chain is drawn as a Fischer projection, a D-monosaccharide has the -OH on this carbon on the right an L monosaccharide has it on the left. [Pg.57]

The p anomer of a d monosaccharide has the OH group drawn up, cis to the CH2OH group at 05. The P anomer is called p-D-glucose, or p-D-glucopyranose (to emphasize the six-membered ring). [Pg.1037]

P Anomer (Section 27.6) The stereoisomer of a cyclic monosaccharide in which the anomerie OH and the CH2OH groups are eis. In a D monosaccharide, the hydroxy group on the anomeric carbon is drawn up. [Pg.1196]

D) monosaccharides are transported to adipose tissue via the lymphatic system. [Pg.29]

Monosaccharides contain at least one asymmetric C atom and are therefore capable of existing in D and L optically active forms (Chapter 13.2). In Table 10.2, the complete scheme of D-monosaccharides is shown, in shortened notation, for up to 6 C atoms. [Pg.831]

For a D-monosaccharide, the terminal —CH2OH points up in the Haworth projection. [Pg.591]

D-monosaccharide one that has the same configuration at its penultimate carbon as L-glyceraldehyde is called an L-monosaccharide. [Pg.607]

Which compounds are D-monosaccharides and which are L-monosaccharides (See Example 17.1)... [Pg.609]

Trehalose is found in young mushrooms and is the chief carbohydrate in the blood of certain insects. Trehalose is a disaccharide consisting of two D-monosaccharide units, each joined to the other by an a-1,1-glycosidic bond ... [Pg.612]

D-Monosaccharide A monosaccharide that, when written as a Fischer projection, has the —OH on its penultimate carbon to the right. [Pg.731]

What is the nature and relative proportion of the A, B, C, D monosaccharides involved in this oligomer, including ring size and their configuration (d- or L-) ... [Pg.6559]

Draw Fischer projections for the four aldotetroses. Which are D-monosaccharides, which are L-monosaccharides, and which are enantiomers Refer to Table 25.1 and write the name of each aldotetrose. [Pg.1094]

A monosaccharide that has the same configuration about its penultimate carbon as D-glyceraldehyde is classified as a D-monosaccharide. In this case, the —OH group is on the right side of the carbon atom in the Fischer projection. [Pg.1113]

Figure 6. Solvent dependence of the first Cotton effect (Xmax nm) of the polyacetylenes bearing pendants of D-monosaccharide acetonides. Data marked with was measured in a mixture ofTHF/CHCls (19 1 by volume). Figure 6. Solvent dependence of the first Cotton effect (Xmax nm) of the polyacetylenes bearing pendants of D-monosaccharide acetonides. Data marked with was measured in a mixture ofTHF/CHCls (19 1 by volume).

See other pages where D-Monosaccharides is mentioned: [Pg.58]    [Pg.305]    [Pg.57]    [Pg.293]    [Pg.184]    [Pg.185]    [Pg.1032]    [Pg.1037]    [Pg.1196]    [Pg.336]    [Pg.370]    [Pg.4]    [Pg.323]    [Pg.85]    [Pg.235]    [Pg.787]    [Pg.4]    [Pg.19]    [Pg.6]    [Pg.148]    [Pg.586]    [Pg.588]    [Pg.588]    [Pg.590]    [Pg.594]    [Pg.594]    [Pg.605]    [Pg.603]    [Pg.1092]    [Pg.1092]    [Pg.1117]    [Pg.1121]    [Pg.6]   
See also in sourсe #XX -- [ Pg.1060 , Pg.1061 ]




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Monosaccharides D-glucose

Monosaccharides d and L designations

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