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- W2950204893 abstract "Photolysis of the azepinone (2) gives the bicyclic photoproduct (5) in 64% yield; this compound reverts cleanly to the starting material (2) on thermolysis in toluene. Cycloaddition reactions of the azepinones (1) or (2) with maleic anhydride generate the endo adducts (7) or (8), respectively, whereas treatment of (1) with acetylenic dienophiles gives rise to benzenoid compounds after cleavage of the three-atom bridge." @default.
- W2950204893 created "2019-06-27" @default.
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- W2950204893 date "2010-08-23" @default.
- W2950204893 modified "2023-09-25" @default.
- W2950204893 title "ChemInform Abstract: Azepinones. Part 4. Electrocyclic and Cycloaddition Reactions of Simple 1H-Azepin-3(2H)-ones." @default.
- W2950204893 cites W2046348362 @default.
- W2950204893 doi "https://doi.org/10.1002/chin.199107164" @default.
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