4.3 Article

Copper-mediated One-pot Synthesis of Trifluorostyrene Derivatives from Tetrafluoroethylene and Arylboronate

Journal

CHEMISTRY LETTERS
Volume 44, Issue 7, Pages 1019-1021

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.150322

Keywords

-

Funding

  1. MEXT [25708018, 23105546]
  2. ACT-C program from the JST
  3. A-STEP program from the JST
  4. Grants-in-Aid for Scientific Research [15H05803, 25708018] Funding Source: KAKEN

Ask authors/readers for more resources

We developed the copper-mediated synthesis of trifluorostyrene derivatives. beta-Fluorine elimination of a 2-aryl-1,1,2,2-tetrafluoroethylcopper complex, generated in situ from aryl-boronate, copper tert-butoxide, and 1,10-phenanthroline with tetrafluoroethylene (TFE) via carbocupration, was promoted by the addition of a Lewis acid. The present reaction system was applied to the one-pot synthesis of various trifluorostyrene derivatives, through the transmetalation carbocupration-beta-fluorine elimination sequence.

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