4.6 Article

Cobalt-Catalyzed C-H Arylations with Weakly-Coordinating Amides and Tetrazoles: Expedient Route to Angiotensin-II-Receptor Blockers

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 15, Pages 5718-5722

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201500552

Keywords

amides; arylation; C-H activation; cobalt; tetrazoles

Funding

  1. European Research Council under the European Community/ERC [307535]
  2. Chinese Scholarship Program

Ask authors/readers for more resources

Cobalt-catalyzed C-H arylations enabled the synthesis of biaryl tetrazoles, which are key structural motifs in antihypertensive angiotensin-II-receptor blockers. Thus, weakly-coordinating benzamides were employed for step-economical C-H arylations with ample scope. Further, a low-valent NHC complex enabled first cobalt-catalyzed C-H functionalization by tetrazole assistance.

Authors

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

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available