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 |
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Format: | Artikel |
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.
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•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. |
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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/j.tet.2024.134125 |