Carbon-13 spin-lattice relaxation studies for resonance assignment to specific, carbon positions of dextrans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference7 articles.
1. Structural analysis of dextrans containing 2-O-α-d-glucosylated α-d-glucopyranosyl residues at the branch points, by use of 13C-nuclear magnetic resonance spectroscopy and gas-liquid chromatography-mass spectrometry
2. Determination of the structure of dextran by 13C-nuclear magnetic resonance spectroscopy
3. High-temperature enhancement of 13C-N.M.R. chemical-shifts of unusual dextrans, and correlation with methylation structural analysis
4. Six unusual dextrans: methylation structural analysis by combined g.l.c.—m.s. of per-O-acetyl-aldononitriles
5. Methylation structural analysis of unusual dextrans by combined gas-liquid chromatography-mass spectrometry
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1. Microbial Polysaccharides;Kirk‐Othmer Encyclopedia of Chemical Technology;2000-12-04
2. Mechanism and action of glucansucrases;Enzymes for Carbohydrate Engineering;1996
3. Mechanisms in The Glucansucrase Synthesis of Polysaccharides and Oligosaccharides From Sucrose;Advances in Carbohydrate Chemistry and Biochemistry;1995
4. Carbon-13 Nuclear Magnetic Relaxation And Motional Behavior of Carbohydrate Molecules In Solution;Advances in Carbohydrate Chemistry and Biochemistry;1995
5. Mechanism and action of glucansucrases;Progress in Biotechnology;1995
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