| Literature DB >> 31242342 |
Andrés García-Domínguez1, Rahul Mondal1, Cristina Nevado1.
Abstract
The potential of merging photoredox and nickel catalysis to perform multicomponent alkene difunctionalizations under visible-light irradiation is demonstrated here. Secondary and tertiary alkyl groups, as well as sulfonyl moieties can be added to the terminal position of the double bond with simultaneous arylation of the internal carbon atom in a single step under mild reaction conditions. The process, devoid of stoichiometric additives, benefits from the use of bench-stable and easy-to-handle reagents, is operationally simple, and tolerates a wide variety of functional groups.Entities:
Keywords: alkenes; multicomponent reactions; nickel; photochemistry; reaction mechanisms
Year: 2019 PMID: 31242342 DOI: 10.1002/anie.201906692
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336