4.6 Article

Efficient [5+1]-strategy for the assembly of 1,8-naphthyridin-4(1H)-ones by domino amination/conjugate addition reactions of 1-(2-chloropyridin-3-yl) prop-2-yn-1-ones with amines

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 10, Issue 15, Pages 2955-2959

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ob07030h

Keywords

-

Funding

  1. BMBF REMEDIS [03IS2081A]

Ask authors/readers for more resources

A facile synthetic approach for the synthesis of 1,8-naphthyridine-4(1H)-one derivatives via a catalyst free and Pd-supported tandem amination sequence is developed and described. In a case of aliphatic amines reaction proceeds in a catalyst free mode, however anilines demand Pd-supported 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

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available