Selenium Transfer from Secondary Phosphine Selenides to Aminoacetylenic Ketones: Access to 1,2-Dihydro‑3H‑pyrrole-3-selones with a Stable CSe Bond
Secondary phosphine selenides were found to react with γ-aminoacetylenic ketones (80–85 °C, MeCN, 17–40 h) to afford 1,2-dihydro-3H-pyrrole-3-selones in 48–80% yields, products of unprecedented selenium transfer from the PSe bond to replace the carbonyl oxygen and to form dihydro-3H-pyrrole-3-selon...
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Veröffentlicht in: | Organic letters 2024-09, Vol.26 (35), p.7336-7340 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Secondary phosphine selenides were found to react with γ-aminoacetylenic ketones (80–85 °C, MeCN, 17–40 h) to afford 1,2-dihydro-3H-pyrrole-3-selones in 48–80% yields, products of unprecedented selenium transfer from the PSe bond to replace the carbonyl oxygen and to form dihydro-3H-pyrrole-3-selones having a CSe bond stable under ambient conditions. |
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ISSN: | 1523-7060 1523-7052 1523-7052 |
DOI: | 10.1021/acs.orglett.4c02491 |