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- W1541640897 abstract "On triplet sensitization (E)-5 gives (Z)-5 and isomerizes via C(δ), O-bond cleavage to the cyclobutanone 6 and the conjugated γ-ketoester 7. - On singulet excitation 6 undergoes decarbonylation and yields the bicyclo [4.1.0]heptane 8. However, on triplet sensitization 6 is converted to the isomeric tricyclononane 9 by a stereospecific oxa-di-π-methane rearrangement. The structure of 9 is determined by X-ray analysis of the p-nitrobenzoate 15: a = 10.573, b = 14.707, c = 13.494 Å, β = 112.40°, P21/n, Z, = 4." @default.
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- W1541640897 date "1980-10-29" @default.
- W1541640897 modified "2023-09-25" @default.
- W1541640897 title "Photochemische Reaktionen. 112. Mitteilung [1] Zur Photochemie ?, ?-unges�ttigter ?, ?-Epoxyester. III. Erg�nzende Untersuchungen zur Triplettreaktivit�t" @default.
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- W1541640897 doi "https://doi.org/10.1002/hlca.19800630712" @default.
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