4.8 Article

Selective, Intermolecular Alkylarylation of Alkenes via Photoredox/Nickel Dual Catalysis

Journal

ORGANIC LETTERS
Volume 21, Issue 12, Pages 4771-4776

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01658

Keywords

-

Funding

  1. National Natural Science Foundation of China [21702029]
  2. Thousand Plan Youth program
  3. Shanghai Sailing Program [17YF1400100]
  4. Fundamental Research Funds for the Central Universities

Ask authors/readers for more resources

A regioselective, intermolecular 1,2-alkylarylation of alkenes with aryl halides and alkyl oxalates has been developed via photoredox/nickel dual catalysis. This dual-catalytic protocol involves a radical relay process, where radical addition is followed by a nickel-assisted coupling, forging two consecutive C-C bonds in a single operation. The mild and redox-neutral conditions allow for good compatibility in the scope of olefins, (hetero)aryl halides, as well as alkyl oxalates.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available