4.8 Article

Synthesis of N-Azolylindoles by Copper-Catalyzed C-H/N-H Coupling-Annulation Sequence of o-Alkynylanilines

Journal

ORGANIC LETTERS
Volume 14, Issue 2, Pages 664-667

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol203392r

Keywords

-

Funding

  1. MEXT
  2. JSPS, Japan
  3. Grants-in-Aid for Scientific Research [22750040] Funding Source: KAKEN

Ask authors/readers for more resources

A wide range of o-alkynylanilines undergo a copper-catalyzed direct C-H/N-H coupling with azoles followed by benzannulation to form the corresponding N-azolylindoles in good yields. The domino reaction proceeds effectively with molecular oxygen as the sole oxidant and provides a new dehydrogenative access to the titled compounds of interest in pharmaceutical and material sciences.

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