Issue 18, 1970

Photo-oxidation of carbanions: the reactivity of singlet oxygen with 9-benzenesulphonylfuoren-9-yl anion

Abstract

The oxidation of 9-substituted fluoren-9-yl anions to fluorenone by molecular oxygen in t-butyl alcohol is markedly accelerated by irradiation of added dye sensitisers (e.g., rose bengal) or by direct excitation of the carbanion, singlet oxygen being involved in both cases.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1178-1179

Photo-oxidation of carbanions: the reactivity of singlet oxygen with 9-benzenesulphonylfuoren-9-yl anion

D. Bethell and R. G. Wilkinson, J. Chem. Soc. D, 1970, 1178 DOI: 10.1039/C29700001178

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