Photochemical Rearrangement of 2,3-Dihydroisoxazoles. Formation of Stable Azomethine Ylides via Acyl Aziridines as Intermediates

DOI: 10.1039/c39940000301

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Journal of the Chemical Society. Chemical communications p. 301 - 302 (1994)

Update date:2022-08-11

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Authors:

Lopez-Calle, Eloisa

Eberbach, Wolfgang

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Article abstract of DOI:10.1039/c39940000301

Irradiation of the 2,3-annulated 2,3-dihydroisoxazoles 3 affords azomethine ylides 4 as isolable compounds, which on heating are transformed into the tetrahydroindolizines 7 and 8.

Full text of DOI:10.1039/c39940000301

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