A Synthetic Route to Tetrahydro-1 H -azepino[4,3,2- cd ]indoles via Ring-Opening Cyclization of Activated Azetidines with 4-Bromoindole: Toward a Vasopressin V2 Receptor Antagonist
A simple one-pot, two-step strategy for the synthesis of tetrahydro-1 -azepino[4,3,2- ]indoles via Lewis acid-catalyzed S 2-type ring opening of activated azetidines with 4-bromoindole, followed by a Pd-catalyzed intramolecular C-N cyclization reaction, with good to excellent yields is described. Ut...
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Veröffentlicht in: | Journal of organic chemistry 2024-08, Vol.89 (16), p.11576-11587 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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