Issue 5, 1984

Sterically protected hemins with electronegative substituents: efficient catalysts for hydroxylation and epoxidation

Abstract

Meso-tetra(2,6-dichlorophenyl)porphinatoiron(III)chloride and meso-tetra(pentachlorophenyl)porphinatioiron(III)chloride, which resist µ-oxo dimmer formation and oxidative destruction, are found to be unusually efficient catalysts for high-turnover, high-yield alkene epoxidation and alkane hydroxylation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 279-280

Sterically protected hemins with electronegative substituents: efficient catalysts for hydroxylation and epoxidation

P. S. Traylor, D. Dolphin and T. G. Traylor, J. Chem. Soc., Chem. Commun., 1984, 279 DOI: 10.1039/C39840000279

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