DIELS-ALDER REACTION OF TETRACYCLONE WITH SOME MALEIMIDES

Tetracyclone I reacts with N-substituted maleimides II to give the adducts III a–f. Dehydrogenation of III c, e, f gave IV a–c. In a similar manner III adds another molecule of either maleic anhydride or N-substituted maleimide to give V a–b and VI a–e respectively. On the other hand, VI b dehydroge...

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Veröffentlicht in:Current science (Bangalore) 1975-11, Vol.44 (22), p.797-800
Hauptverfasser: Khalifa, M. A. E., Abdou, Sadek E. I., Ezzat, M. Zayed
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Sprache:eng
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Zusammenfassung:Tetracyclone I reacts with N-substituted maleimides II to give the adducts III a–f. Dehydrogenation of III c, e, f gave IV a–c. In a similar manner III adds another molecule of either maleic anhydride or N-substituted maleimide to give V a–b and VI a–e respectively. On the other hand, VI b dehydrogenates readily to VII.
ISSN:0011-3891