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Journal ArticleDOI

Nuclear Magnetic Resonance Spectroscopy. Carbon-13 Spectra of Some Inositols and Their O-Methylated Derivatives

Douglas E. Dorman, +2 more
- 01 Mar 1970 - 
- Vol. 92, Iss: 5, pp 1351-1354
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TLDR
In this paper, the C nmr spectra of some inositols and their partially O-methylated derivatives are tabulated and discussed, and a system of empirical constants which can be used to estimate the spectral properties of the carbons of these ring systems is derived.
Abstract
The ^(13)C nmr spectra of some inositols and their partially O-methylated derivatives are tabulated and discussed. Methods of assignment are detailed. A system of empirical constants which can be used to estimate the spectra of the carbons of these ring systems is derived. The substituent effects are noted to conform generally to the notion that steric or proximity effects are very important sources of chemical-shift differences in these systems.

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Journal ArticleDOI

Carbon-13 nmr spectroscopy of tetrapyrroles*

TL;DR: In the present study, chlorophylls a and b uniformly labeled with I3C, and coproporphyrin 111 specifically labeled with 13C are prepared and the proton-noise decoupled CMR spectra have been obtained and interpreted for position assignment.
Journal ArticleDOI

Synthesis of allo- and epi-inositol via the NHC-catalyzed carbocyclization of carbohydrate-derived dialdehydes.

TL;DR: A synthesis of carbocyclic sugars from carbohydrate-derived dialdehydes using organocatalysis has been developed and stereospecifically reduced using sodium borohydride and deprotected to give allo- and epi-inositol in good yield that confirmed the structural and stereochemical assignments.
Journal ArticleDOI

Untersuchung der 13c-kernresonanz-spektren der acht isomeren 1,6-anhydro-β-D-hexopyranosen

TL;DR: In this article, the signals of the 13C-n.m.r. spectra of the 8 isomeric 1,6-anhydro-β-D -hexopyranoses having the 1C4 conformation were assigned by comparison with the spectrum of selectively deuterated derivatives and by observation of the substituent effect of the O-isopropylidene derivatives.
Journal ArticleDOI

Multinuclear magnetic resonance studies of boar seminal plasma

TL;DR: Multinuclear magnetic resonance studies were performed on aqueous solutions of lyophilisates of boar seminal plasma and confirmed the presence of GPC and revealed phosphorylcholine, glycerophosphorylserine and glycerophilelethanolamine as further components.
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