Issue 24, 1994

Enantio-and stereo-selective route to the taxol side chain via asymmetric epoxidation of trans-cinnamyl alcohol and subsequent expoxide ring opening

Abstract

The first route to the side chain of Taxol and Taxotere, employing asymmetric epoxidation (AE) of trans-cinnamyl alochol and a new highly regio- and stereo-selective opening to the epoxide ring with MgBr2, is described.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 2767-2768

Enantio-and stereo-selective route to the taxol side chain via asymmetric epoxidation of trans-cinnamyl alcohol and subsequent expoxide ring opening

C. Bonini and G. Righi, J. Chem. Soc., Chem. Commun., 1994, 2767 DOI: 10.1039/C39940002767

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