4.3 Article Proceedings Paper

Synthesis of Xanthones by Palladium-Catalyzed Tandem Carbonylation/C-H Activation via 2-Iodo Diaryl Ethers

Journal

JOURNAL OF THE CHINESE CHEMICAL SOCIETY
Volume 65, Issue 1, Pages 28-32

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jccs.201700125

Keywords

Xanthone; Palladium-catalyzed reaction; Heterocycle synthesis

Funding

  1. National Natural Science Foundation of China [31301712, 31270388]
  2. Opening Funds of Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

Ask authors/readers for more resources

The ring closure of 2-iodo diaryl ether in the presence of a palladium catalyst to xanthone under carbon monoxide atmosphere is studied. A series of xanthones could be successfully obtained through this protocol, with Pd(OAc)(2) as the catalyst, P(Cy)(3) as ligand, PivONa center dot H2O as base, and PivOH and tetrabutylamonium bromide as additives in DMSO, in moderate to good yields.

Authors

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

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available