 376. Aspects of stereochemistry. Part I. Stereospecificity in formation of epoxides from cyclic allylic alcohols by H. B. Henbest and R. A. L. Wilson

ID: 376-aspects-of-stereochemistry-part-i-stereospecificity-in-formation-of-epoxides-from-cyclic-allylic-alcohols-by-h-b-henbest-and-r-a-l-wilson

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376. Aspects of stereochemistry. Part I. Stereospecificity in formation of epoxides from cyclic allylic alcohols by H. B. Henbest and R. A. L. Wilson by

Codex  0 2026-10-20

doi.org/10.1039/JR9570001958

Journal of the Chemical Society, 1958–1965. Comparison of free allylic alcohols and derivatives demonstrates hydroxyl-directed peracid epoxidation; the cyclic examples support the directing principle rather than constituting a measurement on this exam substrate.

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