Issue 7, 1994

A flexible and rational synthesis of substituted triphenylenes by palladium-catalysed cross-coupling of arylzinc halides

Abstract

A new, flexible route to the substituted triphenylenes has been developed which involves the preparation of terphenyls using a palladium-catalysed cross-coupling of arylzinc halides with 1,2-dihalogenobenzenes, followed by oxidative cyclisation of these terphenyl using ferric chloride.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 845-846

A flexible and rational synthesis of substituted triphenylenes by palladium-catalysed cross-coupling of arylzinc halides

R. C. Borner and R. F. W. Jackson, J. Chem. Soc., Chem. Commun., 1994, 845 DOI: 10.1039/C39940000845

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