Issue 8, 1988

Epoxidation with pyridine–trifluoroacetic anhydride–molecular oxygen and its mechanistic aspects

Abstract

Epoxidation of cholesteryl acetate (3) with pyridine–trifluoroacetic anhydride–molecular oxygen afforded bis(trifluoroacetate)(4), β-epoxide (5], α-epoxide (6), hydroxy trifluoroacetates A (7) and B (9), and enone (8). An oxidation mechanism proceeding via the hydroperoxide intermediate (A) is presented.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1988, 2335-2337

Epoxidation with pyridine–trifluoroacetic anhydride–molecular oxygen and its mechanistic aspects

T. Harayama, O. Sakurai, H. Fukushi, Y. Tezuka and F. Yoneda, J. Chem. Soc., Perkin Trans. 1, 1988, 2335 DOI: 10.1039/P19880002335

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