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
Hauptverfasser: Chen, Bo, Wu, Xiao-Feng
Format: Artikel
Sprache:eng
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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