Palladium(II)/Lewis Acid Cocatalyzed Oxidative Annulation of 2‑Alkenylanilines and Propargylic Esters: An Access to Benzo[b]azepines
An attractive approach to valuable yet synthetically challenging benzo[b]azepines was established via palladium(II)/Lewis acid cocatalyzed oxidative [5 + 2] annulation of readily available 2-alkenylanilines and propargylic esters. The protocol features mild reaction conditions and good functional...
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Veröffentlicht in: | Journal of organic chemistry 2019-09, Vol.84 (17), p.10843-10851 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | An attractive approach to valuable yet synthetically challenging benzo[b]azepines was established via palladium(II)/Lewis acid cocatalyzed oxidative [5 + 2] annulation of readily available 2-alkenylanilines and propargylic esters. The protocol features mild reaction conditions and good functional group tolerance, constituting an array of benzo[b]azepines in yields of 30–75%. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/acs.joc.9b01406 |