Development of the Julia asymmetric epoxidation reaction. Part 1. Application of the oxidation to enones other than chalcones

DOI: 10.1039/P19960000343

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Journal of the Chemical Society. Perkin transactions I p. 343 - 348 (1996)

Update date:2022-08-02

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Authors:

Lasterra-Sanchez, M. Elena

Felfer, Ulfried

Mayon, Patrick

Roberts, Stanley M.

Thornton, Steven R.

Todd, Christine J.

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Article abstract of DOI:10.1039/P19960000343

Asymmetric epoxidation of a variety of enones 3, 6, 8, 10, 12, 14, 16, 18, 21, 22, 26, 28-30 and 36 gives the corresponding oxiranes in good to excellent yield and optical purity. The oxidation medium consists of basic peroxide or sodium perborate or sodi

Full text of DOI:10.1039/P19960000343

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