Issue 10, 1980

Photolysis of thieno-, furo-, and pyrrolo-[b]pyridine N-imides: formation of 3H-1,3-diazepines

Abstract

Photolysis of pyridine N-ethoxycarbonylimides condensed with thiophen, furan, and pyrrole rings on the b-side of the pyridine ring affords the corresponding novel 1H-1,2- and 3H-1,3-diazepines, respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 454-455

Photolysis of thieno-, furo-, and pyrrolo-[b]pyridine N-imides: formation of 3H-1,3-diazepines

T. Tsuchiya, M. Enkaku and S. Okajima, J. Chem. Soc., Chem. Commun., 1980, 454 DOI: 10.1039/C39800000454

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