Iron Catalyzed Highly Enantioselective Epoxidation of Cyclic Aliphatic Enones with Aqueous H2O2

Publication date

2016-03-02

Authors

Cussó, Olaf
Cianfanelli, Marco
Ribas, Xavi
Klein Gebbink, R.J.M.ISNI 0000000388707889
Costas, Miquel

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Advisors

Supervisors

Document Type

Article
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taverne

Abstract

An iron complex with a C1-symmetric tetradentate N-based ligand catalyzes the asymmetric epoxidation of cyclic enones and cyclohexene ketones with aqueous hydrogen peroxide, providing the corresponding epoxides in good to excellent yields and enantioselectivities (up to 99% yield, and 95% ee), under mild conditions and in short reaction times. Evidence is provided that reactions involve an electrophilic oxidant, and this element is employed in performing site selective epoxidation of enones containing two alkene sites.

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Citation

Cussó, O, Cianfanelli, M, Ribas, X, Klein Gebbink, R J M & Costas, M 2016, 'Iron Catalyzed Highly Enantioselective Epoxidation of Cyclic Aliphatic Enones with Aqueous H2O2', Journal of the American Chemical Society, vol. 138, no. 8, pp. 2732–2738. https://doi.org/10.1021/jacs.5b12681