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Collect. Czech. Chem. Commun. 1986, 51, 2158-2166
https://doi.org/10.1135/cccc19862158

An unusual effect of exo-endo configuration on the quantum yield Φ of photochemical rearrangement of 4-R-substituted 8-phenyl-3,5,10-trioxa-9-azabicyclo-[5,3,0]-8-decenes

Lubor Fišeraa, Vladimír Oremusa, Hans-Joachim Timpeb, Ladislav Štibrányia and Peter Zálupskýa

a Department of Organic Chemistry, Slovak Institute of Technology, 812 37 Bratislava, Czechoslovakia
b Department of Photochemistry, Technical University, DDR-4200 Merseburg, G.D.R.

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  • Ghosh Arun K., Belcher Miranda R.: Lewis Acid-Catalyzed Vinyl Acetal Rearrangement of 4,5-Dihydro-1,3-dioxepines: Stereoselective Synthesis of cis- and trans-2,3-Disubstituted Tetrahydrofurans. J. Org. Chem. 2020, 85, 10399. <https://doi.org/10.1021/acs.joc.0c00390>
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  • Timpe H.‐J., Schmidt M., Fišera L'.: Photochemie und Photophysik von 3‐(2‐Isoxazolinyl)‐phenylketonen. J. Prakt. Chem. 1988, 330, 735. <https://doi.org/10.1002/prac.19883300508>