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Highly enantioselective epoxidation catalysts derived from 1,2-diaminocyclohexane

Eric N. Jacobsen, Wei Zhang, Alexander R. Muci, James R. Ecker and Li Deng

*Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, Email:

E. N. Jacobsen, W. Zhang, A. R. Muci, J. R. Ecker, L. Deng, J. Am. Chem. Soc., 1991, 113, 7063-7064.

DOI: 10.1021/ja00018a068


Readily available Mn(III) complexes catalyze alkene epoxidation by bleach in good yields. A highly enantioselective epoxidation catalyst was developed through a logical sequence of ligand modifications.

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Highly Enantioselective, Catalytic Epoxidation of Trisubstituted Olefins

B. D. Brandes, E. N. Jacobsen, J. Org. Chem., 1994, 59, 4378-4380.

Key Words

Jacobsen Epoxidation, Manganese, Bleach

ID: J48-Y1991-530