13C-N.m.r. relaxation times and chemical shifts of the exo and endo isomers of dioxolane-type benzylidene acetals of carbohydrates: determination of the absolute configuration-Reference-Cited by-同舟云学术

13C-N.m.r. relaxation times and chemical shifts of the exo and endo isomers of dioxolane-type benzylidene acetals of carbohydrates: determination of the absolute configuration

Published:1977-10 Issue:2 Volume:58 Page:C7-C9
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Neszmélyi András,Lipták András,Nánási Pál

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference11 articles.

1. A 13C NMR chemical shift study of trans-fused bicyclic hexopyranoside derivatives

2. Synthese und Impuls-Fourier-Transform-13C-NMR-Untersuchungen verzweigter Kohlenhydrate

3. Synthesis of macrolide antibiotics. I. Stereospecific addition of methyllithium and methylmagnesium iodide to methyl .alpha.-D-xylo-hexopyranosid-4-ulose derivatives. Determination of the configuration at the branching carbon atom by carbon-13 nuclear magnetic resonance spectroscopy

4. 616. Aspects of stereochemistry. Part XXI. Absolute configuration of benzylidene derivatives of some acyclic polyhydric alcohols

5. Hydrogenolysis of the dioxolan type - and - benzylidene derivatives of carbohydrates with the LiAlH4-AlCl3 reagent

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