| Literature DB >> 34342468 |
Andrew C Jones1, William I Nicholson1, Jamie A Leitch2, Duncan L Browne2.
Abstract
The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-milling is herein described. Under a mechanochemical manifold, the reductive C-C bond formation was achieved in the absence of bulk solvent and air/moisture sensitive setups, in reaction times of 2 h. The mechanical action provided by ball milling permits the use of a range of zinc sources to turnover the nickel catalytic cycle, enabling the synthesis of 28 cross-electrophile coupled products.Entities:
Year: 2021 PMID: 34342468 DOI: 10.1021/acs.orglett.1c02096
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005