Issue 22, 1974

Synthesis and photochemical behaviour of 3H-1,2-benzodiazepines

Abstract

The previously unknown 3H-1,2-benzodiazepines (3) are prepared from the 1H-isomers (1) in high yields and the energy barriers to ring inversion are estimated from n.m.r. spectral data; irradiation of the diazepines (3) affords 3-vinylindazole and indenes.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 936-937

Synthesis and photochemical behaviour of 3H-1,2-benzodiazepines

J. Kurita and T. Tsuchiya, J. Chem. Soc., Chem. Commun., 1974, 936 DOI: 10.1039/C39740000936

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