4.5 Article

Synthesis of Oxindoles through Silver-Catalyzed Trifluoromethylation-, Difluoromethylation- and Arylsulfonylation-Cyclization Reaction of N-Arylacrylamides

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2014, Issue 15, Pages 3196-3202

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201400087

Keywords

Synthetic methods; Homogenous catalysis; Nitrogen heterocycles; Silver

Funding

  1. National Natural Science Foundation of China (NSFC) [21072051]
  2. NCET program [NCET-09-0334]
  3. Fundamental Research Funds for the Central Universities, Hunan University

Ask authors/readers for more resources

Efficient synthesis of trifluoromethyl and difluoromethyl-substituted oxindoles was achieved by reacting Langlois reagent or Baran reagent with N-arylacrylamides. However, the reaction of aryl sulfinic acid sodium salts with N-arylacrylamides did not give the desulfinative products, instead, aryl sulfonated products were produced.

Authors

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

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available