Issue 12, 1974

Conformation and stability of 1,1-diphenylmethyleneiminyl

Abstract

The magnitudes of ring-proton coupling in the title radical are consistent with those calculated for the conformation (III) which is also estimated to be the most stable rotamer.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 488-489

Conformation and stability of 1,1-diphenylmethyleneiminyl

R. F. Hudson, A. J. Lawson and K. A. F. Record, J. Chem. Soc., Chem. Commun., 1974, 488 DOI: 10.1039/C39740000488

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