A new electrochemical system for stereoselective allylic hydroxylation of cholesteryl acetate with dioxygen induced by iron picolinate complexes

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Abstract

The oxygenation reaction of cholesteryl acetate 1 was examined with the FeIII(PA)3/O2/MeCN system using an electrochemical method. The constant potential technique gave mainly the 7-hydroxylated product stereoselectively, along with the 7-oxo product. This oxygenation system is mechanistically unique, requiring iron catalyst, dioxygen, and both cathode and anode. © 2004 Pharmaceutical Society of Japan.

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Okamoto, I., Funaki, W., Nakaya, K., Kotani, E., & Takeya, T. (2004). A new electrochemical system for stereoselective allylic hydroxylation of cholesteryl acetate with dioxygen induced by iron picolinate complexes. Chemical and Pharmaceutical Bulletin, 52(6), 756–759. https://doi.org/10.1248/cpb.52.756

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