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

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

Chemical & pharmaceutical bulletin (2004-06-10)
Iwao Okamoto, Wataru Funaki, Kyosuke Nakaya, Eiichi Kotani, Tetsuya Takeya
ABSTRAKT

The oxygenation reaction of cholesteryl acetate 1 was examined with the Fe(III)(PA)(3)/O(2)/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.

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Sigma-Aldrich
Cholesteryl acetate, 97%