4.7 Article

Synthesis of Isoquinolones by Sequential Suzuki Coupling of 2-Halobenzonitriles with Vinyl Boronate Followed by Cyclization

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 86, Issue 12, Pages 8479-8488

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.1c00472

Keywords

-

Funding

  1. NIH [R35CA197589, F31CA232477, 5T32GM067543]
  2. American Cancer Research Professorship

Ask authors/readers for more resources

A novel and facile two-step synthesis method for 3,4-unsubstituted isoquinolin-1(2H)-ones is described, involving a Suzuki cross-coupling reaction and platinum-catalyzed nitrile hydrolysis and cyclization.
A novel, facile, and expeditious two-step synthesis of 3,4-unsubstituted isoquinolin-1(2H)-ones from a Suzuki cross-coupling between 2-halobenzonitriles and commercially available vinyl boronates followed by platinum-catalyzed nitrile hydrolysis and cyclization is described.

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