PREFERENCE FOR PHOTODISSOCIATION OVER INTERNAL -CYCLOADDITION DURING IRRADIATION OF AN UNSATURATED α,β-ENONE

DOI: 10.1016/S0040-4039(00)75784-4

Source and publish data:

Tetrahedron Letters p. 663 - 664 (1994)

Update date:2022-08-03

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Authors:

Corey, E. J.

Wu, Laurence I.

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Article abstract of DOI:10.1016/S0040-4039(00)75784-4

Irradiation of 2, its trimethylsilyl ether or acetate ester using ultraviolet light of wavelength > 290 nm results not in internal olefin-α,β-enone cycloaddition, but exclusively in photodissociation either of the intercyclic bond (for 2 or the TMS ether)

Full text of DOI:10.1016/S0040-4039(00)75784-4

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