4.7 Article

Nickel-catalyzed selective C-5 fluorination of 8-aminoquinolines with NFSI

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 4, Issue 8, Pages 1528-1532

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7qo00211d

Keywords

-

Funding

  1. Department of Science & Technology of Jilin Province [20170414052GH]
  2. National Natural Science Foundation of China (NSFC) [51573069]

Ask authors/readers for more resources

The first nickel-catalyzed C-H selective fluorination of 8-aminoquinoline derivatives at the C-5 position was achieved using NFSI (N-fluorobenzenesulfonimide) as the F source and NiSO4 as the catalyst. This method demonstrated broad substrate tolerance under mild conditions and a plausible SET (single electron transfer) mechanism was suggested in the proposal of a radical process.

Authors

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

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available