Copper acetate - Iodine co-mediated thiolation of 2-arylpyridines with thiophenol
Copper acetate - iodine co-mediated regioselective ortho-arylthiolation of 2-arylpyridines has been accomplished with inexpensive and convenient thiophenol as the arylthiolating reagent. This protocol features excellent functional group tolerance, generating thioarylated products in moderate-to-high...
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Veröffentlicht in: | Tetrahedron 2022-01, Vol.103, p.132552, Article 132552 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Copper acetate - iodine co-mediated regioselective ortho-arylthiolation of 2-arylpyridines has been accomplished with inexpensive and convenient thiophenol as the arylthiolating reagent. This protocol features excellent functional group tolerance, generating thioarylated products in moderate-to-high yields. © 2021 Elsevier Science. All rights reserved.
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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/j.tet.2021.132552 |