Claude S. Hudson, etc.'s Advances in Carbohydrate Chemistry, Vol. 5 PDF

By Claude S. Hudson, etc.

ISBN-10: 012007205X

ISBN-13: 9780120072057

Show description

Read or Download Advances in Carbohydrate Chemistry, Vol. 5 PDF

Similar biochemistry books

Download e-book for iPad: Biochemical Calculations: How to Solve Mathematical Problems by Irwin H. Segel

I obtained this e-book for the category. It valuable booklet for knowing and use normally principles for resolve biochemical difficulties.

Download e-book for kindle: Molecular Toxicology Protocols by David H. Phillips, Alan Hewer, Volker M. Arlt (auth.),

A set of state of the art options for examining genotoxic publicity and detecting the ensuing organic effects-including endogenous metabolites-up to and together with the advance of melanoma. The authors emphasize analytical tools that may be in particular utilized to human populations and sufferers.

Read e-book online Molecular Basis of Lysosomal Storage Disorders PDF

Molecular foundation of Lysosomal garage issues summary: Molecular foundation of Lysosomal garage issues

Additional resources for Advances in Carbohydrate Chemistry, Vol. 5

Example text

Chem. , in press. DESULFURIZATION BY RANEY NICKEL 19 Methanolysis of dihydrostreptomycin with subsequent acetylation of the products was found by Brink, Kuehl, Flynn and Folkers6' to give both anomeric forms of methyl pentaacetyldihydrostreptobiosaminide (LVI). Mercaptolysis of either of these anomers, followed by reacetylation, converted them into ethyl pentaacetylthiodihydrostreptobiosaminide (LVII) which was not isolated but immediately desulfurized to the acetylated anhydride LVIII, pentaacetyldihydrodesoxystreptobiosamine.

The crystals were filtered, washed with alcohol and ether and dried in vacm at 70". 8 g. c. -The synthetic sucrose1zobtained from a-D-glucose-1-phosphate and D-fructose through the action of the partially purified sucrose phosphorylase from Pseudomonas saccharophila possesses properties identical with those of natural sucrose. Its empirical formula obtained by elementary analysis is ClrHzaOll. The compound does not reduce Fehling solution before hydrolysis. ,After acid or enzymatic hydrolysis the phenylosaeone obtained from the inversion mixture is D-glucosaeone; the hydrolyzate also gives a positive Seliwanoff reaction for a ketose.

29 31 33 35 36 36 36 37 38 39 41 41 43 43 46 I. INTRODUCTION Sucrose is commercially the most important and quantitatively the most abundant sugar in the vegetable kingdom. It is readily formed as the result of the photosynthetic activity of practically all higher plants, constituting a reserve material used in cell respiration. The energy that is liberated in the latter process is utilized for metabolic activities of the plant such as in the synthesis of numerous organic compounds, including especially amino acids, proteins and fats.

Download PDF sample

Advances in Carbohydrate Chemistry, Vol. 5 by Claude S. Hudson, etc.

by Joseph

Rated 4.74 of 5 – based on 10 votes