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4-O-Methyl-D-galactose

A methylation analysis of S14, performed in the authors laboratory,44 gave 2,3,4,6-tetra-O-methyl-D-galactose, 2,4,6-tri-O-methyl-D-galactose, and 2,3,6-tri-O-methyl-D-glucose in the proportions 1 1 1. Although these are the same components as previously reported, the proportions are different. In addition to these sugars, 2-deoxy-3-0-methyl-2-(methylamino)-D-glucose was also obtained. [Pg.313]

Methylation and hydrolysis of lactose gives a tetra-O-methyl-D-galactose and 2,3,6-tri-O-methyl-D-glucose. The same galactose derivative can be obtained from the methylation and hydrolysis of D-galactopyranose. [Pg.932]

Tri-O-methyl-D-galactose-(6 —> 1) 2,3,4-tri-O-methyl-D-glucosiduronic acid Acacia pycnantha gum B 0 70c... [Pg.142]

As part of his monumental study20 on stachyose, Onuki converted manninotrionic acid into its completely methylated derivative, which he hydrolyzed, to obtain methylated D-galactoses and methylated D-gluconic acid. These products were isolated and identified by Onuki as 2,3,4,6-tetra-O-methyl-D-galactose, 2,3,4-tri-O-methyl-D-galactose and 2,3,5,6-tetra-O-methyl-D-gluconic acid. From these findings, Onuki proposed that manninotriose is... [Pg.172]

Methylation of stachyose and subsequent hydrolysis, by Onuki,20 gave 2,3,4,6-tetra-O-methyl-D-galactose (identified as the crystalline anilide), a tri-O-methyl-D-galactose and a tri-O-methyl-D-glucose (which were converted into the 2,3,4,6-tetra-O-methyl derivatives, and characterized as the crystalline anilides), and 1,3,4,6-tetra-O-methyl-D-fructose, a sirup which agreed in properties with the authentic material. [Pg.178]

Complete structural analysis of galactinol by the methylation method was reported66 by Kabat and associates in 1953. On hydrolysis, completely methylated galactinol gives 2,3,4,6-tetra-O-methyl-D-galactose (identified as the anilide) and 2,3,4,5,6-penta-O-methyl-D-myo-inositol (identified by oxidation to the penta-O-methylinosose, reduction, and demethylation, to give mpo-inositol and L-inositol). [Pg.182]

Recently, Putman and Hassid have confirmed93 the structural formula given by Colin and Gueguen. Methylation of floridoside, followed by hydrolysis, gave 2,3,4,6-tetra-O-methyl-D-galactose and 1,3-di-O-methyl-glyceritol (identified by its lack of optical rotation, and by mixed melting point of its p-nitrobenzoate with the authentic ester). Periodate-oxidation studies on floridoside also confirmed the earlier formula. [Pg.182]

Di-O-methyl-D-galactose, 4-O-methyl-D-mannose, methyl /3-L-arabinoside 0.32... [Pg.351]


See other pages where 4-O-Methyl-D-galactose is mentioned: [Pg.29]    [Pg.351]    [Pg.129]    [Pg.251]    [Pg.132]    [Pg.279]    [Pg.168]    [Pg.29]    [Pg.351]    [Pg.129]    [Pg.251]    [Pg.132]    [Pg.279]    [Pg.168]    [Pg.257]    [Pg.301]    [Pg.304]    [Pg.308]    [Pg.309]    [Pg.310]    [Pg.312]    [Pg.315]    [Pg.316]    [Pg.147]    [Pg.263]    [Pg.264]    [Pg.265]    [Pg.266]    [Pg.484]    [Pg.29]    [Pg.332]    [Pg.19]    [Pg.137]    [Pg.138]    [Pg.139]    [Pg.141]    [Pg.141]    [Pg.141]    [Pg.165]    [Pg.178]    [Pg.351]    [Pg.351]    [Pg.352]    [Pg.352]    [Pg.176]   
See also in sourсe #XX -- [ Pg.132 ]




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2.3.4.6- Tetra-O-methyl-D-galactose

2.4- Di-O-methyl-D-galactose

2.4.6- Tri-O-methyl-D-galactose

D Galactose

Galactose methylation

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