Issue 9, 1988

Anomalous hydrolysis behaviour of [n.n] paracyclophanediazonium salts: a new route to bridged benzobarrelenes

Abstract

The hydrolysis of diazotized 5-amino-[3.3]paracyclophane and anti-4-amino[2.2](1,4)naphthalenoparacyclophane gives products having a barrelene structure, presumably via an aryne mechanism.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 575-576

Anomalous hydrolysis behaviour of [n.n] paracyclophanediazonium salts: a new route to bridged benzobarrelenes

N. Mori, T. Takemura and K. Tsuchiya, J. Chem. Soc., Chem. Commun., 1988, 575 DOI: 10.1039/C39880000575

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