Issue 0, 1971

Aromatic substitution of olefins. Part XI. Reaction of p-substituted dideuteriostyrenes with benzene in the presence of palladium(II) acetate: a mechanistic study

Abstract

The phenylation of [ββ-2H2]styrenes with benzene was carried out in the presence of palladium(II) acetate and acetic acid. From the deuterium analyses of the trans-stilbenes formed, it was confirmed that no hydride shift takes place in the reaction.

Article information

Article type
Paper

J. Chem. Soc. B, 1971, 196-198

Aromatic substitution of olefins. Part XI. Reaction of p-substituted dideuteriostyrenes with benzene in the presence of palladium(II) acetate: a mechanistic study

S. Danno, I. Moritani, Y. Fujiwara and S. Teranishi, J. Chem. Soc. B, 1971, 196 DOI: 10.1039/J29710000196

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