| Literature DB >> 27990726 |
Hong Yi1, Linbin Niu1, Chunlan Song1, Yiying Li1, Bowen Dou1, Atul K Singh1, Aiwen Lei1,2.
Abstract
Direct cross-coupling between alkenes/R-H or alkenes/RXH is a dream reaction, especially without external oxidants. Inputting energy by photocatalysis and employing a cobalt catalyst as a two-electron acceptor, a direct C-H/X-H cross-coupling with H2 evolution has been achieved for C-O and C-N bond formation. A new radical alkenylation using alkene as the redox compound is presented. A wide range of aliphatic alcohols-even long chain alcohols-are tolerated well in this system, providing a new route to multi-substituted enol ether derivatives using simple alkenes. Additionally, this protocol can also be used for N-vinylazole synthesis. Mechanistic insights reveal that the cobalt catalyst oxidizes the photocatalyst to revive the photocatalytic cycle.Entities:
Keywords: C−N bond formation; C−O bond formation; oxidant-free; photocatalysis; radical alkenylation
Year: 2016 PMID: 27990726 DOI: 10.1002/anie.201609274
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336