Issue 0, 1971

Synthesis and proton magnetic resonance spectra of substituted biphenyls

Abstract

A series of new acylamino-, amino-, chloro-, and nitro-derivatives of 3,3′-dichlorobiphenyl have been prepared from 3,3′-dichlorobenzidine, and their structures have been confirmed by 1H n.m.r. spectroscopy. The electronic and steric effects of a nitro-group ortho to the internuclear linkage are discussed.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 762-764

Synthesis and proton magnetic resonance spectra of substituted biphenyls

P. W. Hickmott and A. T. Hudson, J. Chem. Soc. C, 1971, 762 DOI: 10.1039/J39710000762

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