| Literature DB >> 29446875 |
Shang-Zheng Sun1, Ruben Martin1,2.
Abstract
A nickel-catalyzed reductive arylation of ambiphilic α-bromoalkyl boronic esters with aryl halides is described. This platform provides an unrecognized opportunity to promote the catalytic umpolung reactivity of ambiphilic reagents with aryl halides, thus unlocking a new cross-coupling strategy that complements existing methods for the preparation of densely functionalized alkyl-substituted organometallic reagents from simple and readily accessible precursors.Entities:
Keywords: C−C bond formation; boron; cross-coupling; nickel; umpolung
Year: 2018 PMID: 29446875 DOI: 10.1002/anie.201712428
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336