Issue 0, 1967

Proton magnetic resonance spectra of substituted 6,7-dimethoxycinnolines

Abstract

The n.m.r. spectra of 6- and 6,7-substituted cinnolines have been analysed; they confirm the chemical findings of other workers on the position of alkylation of 4-hydroxycinnolines, and the assignments of protons in the cinnolines. The relative values of chemical shifts in deuteriochloroform and other solvents are discussed.

Article information

Article type
Paper

J. Chem. Soc. B, 1967, 1285-1287

Proton magnetic resonance spectra of substituted 6,7-dimethoxycinnolines

A. W. Ellis and A. C. Lovesey, J. Chem. Soc. B, 1967, 1285 DOI: 10.1039/J29670001285

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