4.8 Article

Iridium(III)-Catalyzed One-Pot Access to 1,2-Disubstituted Benzimidazoles Starting from Imidamides and Sulfonyl Azides

Journal

ORGANIC LETTERS
Volume 19, Issue 16, Pages 4343-4346

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b02028

Keywords

-

Funding

  1. National Natural Science Foundation of China [21572072, 21602064]
  2. Xiamen Southern Oceanographic Center [15PYY052SF01]
  3. Science and Technology Bureau of Xiamen City [3502Z20150054]

Ask authors/readers for more resources

A novel Ir-catalyzed annulation of imidamides with sulfonyl azides has been developed. 1,2-Disubstituted benzimidazoles could be easily obtained in up to 99% yield for more than 40 examples. The products further streamline the synthesis of molecules that are important building blocks for organic synthesis and drug discovery. This strategy features high regioselectivity, efficieney, good tolerance of functional groups, and Mild reaction conditions.

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