Miyaura Borylation and One-Pot Two-Step Homocoupling of Aryl Chlorides and Bromides under Solvent-Free Conditions

Solvent‐free protocols for Miyaura borylation and the one‐pot, two‐step homocoupling of aryl halides are reported for the first time. Bis(dibenzylideneacetone)palladium(0) [Pd(dba)2] is an optimal source of palladium for Miyaura borylation, while for one‐pot two‐step homocoupling palladium(II) aceta...

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Veröffentlicht in:Advanced synthesis & catalysis 2016-03, Vol.358 (6), p.977-983
Hauptverfasser: Dzhevakov, Pavel B., Topchiy, Maxim A., Zharkova, Daria A., Morozov, Oleg S., Asachenko, Andrey F., Nechaev, Mikhail S.
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Sprache:eng
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Zusammenfassung:Solvent‐free protocols for Miyaura borylation and the one‐pot, two‐step homocoupling of aryl halides are reported for the first time. Bis(dibenzylideneacetone)palladium(0) [Pd(dba)2] is an optimal source of palladium for Miyaura borylation, while for one‐pot two‐step homocoupling palladium(II) acetate [Pd(OAc)2] gives highest yields. Aryl bromides are coupled most efficiently using the DPEphos ligand. Chlorides are coupled using XPhos. The developed protocols are robust, versatile and easily reproducible on a large scale.
ISSN:1615-4150
1615-4169
DOI:10.1002/adsc.201500844