Issue 6, 1995

A new electrosynthesis of 2,2-dimethylchromenes from 2-(1-bromo-1-methylethyl)benzofurans

Abstract

Electrolytic reduction of 2-(1-bromo-1-methylethyl)benzofurans in acetonitrile affords the corresponding 2,2-dimethylchromenes in good yields even in the absence of a proton donor and comprises the cleavage of a carbon–bromine bond followed by ring expansion.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 615-616

A new electrosynthesis of 2,2-dimethylchromenes from 2-(1-bromo-1-methylethyl)benzofurans

M. Tsukayama, H. Utsumi and A. Kunugi, J. Chem. Soc., Chem. Commun., 1995, 615 DOI: 10.1039/C39950000615

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