Oxidative cross-coupling between secondary phosphine selenides and thiols or dithiols: a facile regio-selective synthesis of thioselenophosphinic S-esters and S-diesters
Reactions between secondary phosphine selenides and a wide range of aliphatic, aromatic and heteroaromatic thiols or dithiols proceed in the Et3N/CCl4 oxidative system under mild conditions (rt 1–3h) to give thioselenophosphinic S-esters or S-diesters in 80–92% isolated yields.
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Veröffentlicht in: | Tetrahedron letters 2013-07, Vol.54 (27), p.3543-3545 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Reactions between secondary phosphine selenides and a wide range of aliphatic, aromatic and heteroaromatic thiols or dithiols proceed in the Et3N/CCl4 oxidative system under mild conditions (rt 1–3h) to give thioselenophosphinic S-esters or S-diesters in 80–92% isolated yields. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2013.04.117 |