Nickel/Cobalt-Catalyzed C(sp3)–C(sp3) Cross-Coupling of Alkyl Halides with Alkyl Tosylates

The C­(sp3)–C­(sp3) cross-coupling of alkyl halides with alkyl tosylates has been developed by employing a combination of nickel and nucleophilic cobalt catalysts in the presence of a manganese reductant. This method provides a straightforward route to a diverse set of not only secondary–primary but...

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Veröffentlicht in:ACS catalysis 2019-10, Vol.9 (10), p.9285-9291
Hauptverfasser: Komeyama, Kimihiro, Michiyuki, Takuya, Osaka, Itaru
Format: Artikel
Sprache:eng
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Zusammenfassung:The C­(sp3)–C­(sp3) cross-coupling of alkyl halides with alkyl tosylates has been developed by employing a combination of nickel and nucleophilic cobalt catalysts in the presence of a manganese reductant. This method provides a straightforward route to a diverse set of not only secondary–primary but also primary–primary C­(sp3)–C­(sp3) linkages under mild conditions without using alkyl-metallic reagents. Mechanistic studies suggest the formation of alkyl radicals from both alkyl halides and alkyl tosylates. Additionally, cross-coupling could be applied to the short-step synthesis of a histone deacetylase inhibitor, Vorinostat.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.9b03352