Issue 1, 1978

Aromatic hydroxylation by O(3P) atoms on γ-radiolysis of liquid carbon dioxide solutions of alkylbenzenes

Abstract

Hydroxylated products have been produced by the attack of O(3P) atoms, generated by γ-radiolysis of liquid CO2, on alkylbenzene at the following sites: aromatic methine carbon, aromatic ring carbon bearing a substituent accompanied by 1,2-shift of the substituent (NIH shift) or removal of the substituent, and alkyl substituent.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 16-18

Aromatic hydroxylation by O(3P) atoms on γ-radiolysis of liquid carbon dioxide solutions of alkylbenzenes

A. Hori, H. Matsumoto, S. Takamuku and H. Sakurai, J. Chem. Soc., Chem. Commun., 1978, 16 DOI: 10.1039/C39780000016

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