Base-mediated [4 + 3] annulation of α-halogen hydroximate with o-QMs: Facile access to 1, 4-benzoxazepine scaffold
AN efficient and facile approach to 1, 4-benzoxazepine was developed from α-halogen hydroximate and o-QMs. This protocol underwent formal [4 + 3] annulation process smoothly under mild reaction conditions to afford the desired products in moderate to excellent yields. A plausible mechanism was propo...
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Veröffentlicht in: | Tetrahedron letters 2024-02, Vol.136, p.154911, Article 154911 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | AN efficient and facile approach to 1, 4-benzoxazepine was developed from α-halogen hydroximate and o-QMs. This protocol underwent formal [4 + 3] annulation process smoothly under mild reaction conditions to afford the desired products in moderate to excellent yields. A plausible mechanism was proposed
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An efficient and facile approach to 1, 4-benzoxazepine was developed from α-halogen hydroximate and o-QMs. This protocol underwent formal [4 + 3] annulation process smoothly under mild reaction conditions to afford the desired products in moderate to excellent yields. A plausible mechanism was proposed. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2024.154911 |