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Gulose

Once the eight Fischer projections have been written they are named m order with the aid of the sentence All altruists gladly make gum m gallon tanks The words of the sentence stand for allose altrose glucose mannose gulose idose galactose talose... [Pg.1032]

There is another sugar (+) gulose that gives the same aldanc acid on oxidation as does (+) glucose... [Pg.1068]

Guinea worms Guimer-Preston zones Guinier radius L-Gulose [6027-89-0]... [Pg.457]

D-Allose D-Altrose D-Glucose -Mannose D-Gulose D-ldose -Galactose D-Talose... [Pg.474]

Most substrates, with the exception of hydroxypymvate, have a threo configuration of hydroxyl groups at the C-3 and C-4 positions (139). The new stereocenter formed in TK-catalyzed addition is formed in the threo configuration with high diastereo-selectivity (151). Using TK-catalyzed condensations of hydroxypymvic acid with a number of aldehydes a practical preparative synthesis of L-idose [5934-56-5], L-gulose [6027-89-0], 2-deoxy-L-xylohexose, and... [Pg.346]

The aldohexoses are allose, altrose, glucose, mannose, gulose, idose, galactose, and talose. The mnemonic All altruists gladly make gum in gallon tanks is helpful in writing the conect Fischer projection for each one. [Pg.1061]

Problem 25.18 I Reduction of L-gulose with NaBH4 leads to the same alditol (D-glucitol) as reduction of D-glucose. Explain. [Pg.992]

Problem 25.22 What aldopentose would give a mixture of L-gulose and L-idose on Kiliani-Fischer chain extension ... [Pg.995]

Y. pseudotuberculosis VB, however, the same sugar is a-furanosidic. The LPS from other species of Yersinia contain 6-deoxy-o-gulose, which is a-pyranosidic in the LPS from Y. enterocolitica serovar 0 6,31. [Pg.284]

Before 1983, branched-chain sugars had not been found in bacterial polysaccharides, but there are now five examples belonging to this class. The LPS from Coxiella burned phase I contains both 6-deoxy-3-C-methyl-L-gulose (L-virenose) as pyranoside (12) and 3-C-(hydroxymethyl)-L-lyxose as furan-oside (13). Another 6-deoxy-3-C-methylhexose, having the manno configuration, is a component of the Nitrobacter hamburgiensis 0-antigen. ... [Pg.287]

C13-0018. Gulose is a six-carbon sugar that differs from glucose in two positions. In gulose the hydroxyl... [Pg.932]

Carbon atom D-Gulose Me a-D-guIoside D-Mannose Me a-D-mannoside... [Pg.48]

C16H3oOsS2 2,3 4,5-Di-0-isopropylidene-D-gulose diethyl dithioacetal (IPGETA)97... [Pg.247]


See other pages where Gulose is mentioned: [Pg.18]    [Pg.18]    [Pg.196]    [Pg.204]    [Pg.1066]    [Pg.1250]    [Pg.1066]    [Pg.981]    [Pg.982]    [Pg.1011]    [Pg.1300]    [Pg.293]    [Pg.311]    [Pg.313]    [Pg.793]    [Pg.121]    [Pg.160]    [Pg.172]    [Pg.173]    [Pg.59]    [Pg.932]    [Pg.248]    [Pg.18]    [Pg.47]    [Pg.247]    [Pg.397]    [Pg.221]    [Pg.66]    [Pg.67]    [Pg.67]    [Pg.72]   
See also in sourсe #XX -- [ Pg.17 ]




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6-Deoxy-D-gulose

D Gulose

Gulose 2,6-dideoxy

Gulose 6-deoxy

Gulose Fischer projection

Gulose aqueous solution

Gulose derivatives, synthesis

Gulose preparation

Gulose pyranose form

Gulose solution

Gulose synthesis

Gulose, 2-amino-2-deoxy

Gulose, configuration

L-Gulose

N-Gulose

Of D-gulose

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