Synthesis of novel bis(spirocyclic-2-oxindole)-tethered 10b-azachrysene or 10a-azaphenanthrene systems via a Hantzsch-like reaction

The effective synthesis of bis(spirocyclic-2-oxindole) tethered to 10b-azachrysene or 10a-azaphenanthrene moieties via the Hantzsch-like reaction of phenylenebis(methylene))bis(indoline-2,3-diones) and 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile with either 5,5-dimethylcyclohexane-1,3-...

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Veröffentlicht in:Tetrahedron 2024-08, Vol.162, p.134125, Article 134125
Hauptverfasser: Abdelmoniem, Amr M., Abdelhamid, Ismail A., Elwahy, Ahmed H.M., Abdelrahman, Mohamed G.M., Hassaneen, Hamdi M., Teleb, Mohamed A.Mohamed
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Sprache:eng
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Zusammenfassung:The effective synthesis of bis(spirocyclic-2-oxindole) tethered to 10b-azachrysene or 10a-azaphenanthrene moieties via the Hantzsch-like reaction of phenylenebis(methylene))bis(indoline-2,3-diones) and 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile with either 5,5-dimethylcyclohexane-1,3-dione or 3-aminocrotononitrile in acetic acid at reflux is reported. [Display omitted] •Hantzsch-like reaction.•Utility of phenylenebis(methylene))bis(indoline-2,3-diones) and 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile as precursors.•Synthesis of bis(spirocyclic-2-oxindole) tethered to 10b-azachrysene moiety.•Synthesis of bis(spirocyclic-2-oxindole) tethered to 10a-azaphenanthrene moiety.
ISSN:0040-4020
1464-5416
DOI:10.1016/j.tet.2024.134125