Manganese()-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters
A Mn( iii )-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc) 3 ·2H 2 O as the promotor, a broad range of thioesters were...
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Veröffentlicht in: | Organic & biomolecular chemistry 2021-11, Vol.19 (44), p.9654-9658 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
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Zusammenfassung: | A Mn(
iii
)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc)
3
·2H
2
O as the promotor, a broad range of thioesters were synthesized in good to excellent yields
via
radical intermediates.
A Mn(
iii
)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. |
---|---|
ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/d1ob01960k |