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Journal ArticleDOI

Carbon-13 Magnetic Resonance Studies of Azoles. Tautomerism, Shift Reagent Effects, and Solvent Effects

José Elguero, +2 more
- 01 Feb 1974 - 
- Vol. 39, Iss: 20, pp 357-363
TLDR
The effects of substitution, lanthanide-shift reagents, solvent changes, and tautomerism were investigated in this article, where it was concluded that chemical shifts are of limited value to ascertain the positions of tautomers.
Abstract
The effects of substitution, lanthanide-shift reagents, solvent changes, and tautomerism were investigated on the ^(13)C chemical shifts of pyrrole, pyrazole, imidazole, s- and v-triazole, and tetrazole. It was concluded that ^(13)C chemical shifts are of limited value to ascertain the positions of tautomeric equilibrium for rapidly interconverting azole tautomers.

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Journal ArticleDOI

N‐polyazolylmethanes. 1. Synthesis and nmr study of N,N′‐diazolylmethanes

TL;DR: In this paper, the relative amounts of isomeric mixtures obtained with asymmetric azoles or with equimolar mixtures of azoles are compared with literature results on monoalkylation of azole.
Book ChapterDOI

Recent Advances in Tetrazole Chemistry

TL;DR: In this paper, the development of tetrazole chemistry from 1965 to 1975 is discussed, including the applications of modern physical techniques to tetrazoles derivatives and studies of pharmacologically active tetrazolines, particularly replacement of the carboxylic acid group in known active molecules by its analog.
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