THERMAL AND PHOTOCHEMICAL REACTIONS OF UNSATURATED BICYCLIC ENDOPEROXIDES

DOI: 10.1016/S0040-4039(00)89142-X

Source and publish data:

Tetrahedron Letters p. 803 - 806 (1985)

Update date:2022-08-16

Topics:

Authors:

Carless, Howard A. J.

Atkins, Robert

Fekarurhobo, G. K.

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Article abstract of DOI:10.1016/S0040-4039(00)89142-X

Thermal, and especially photochemical, rearrangement of the endoperoxides (1) and (5)-(11) gives βγ-epoxycycloalkanones as primary products, accompanied by the expected syn-diepoxides.

Full text of DOI:10.1016/S0040-4039(00)89142-X

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