4.8 Article

Visible-Light Induced Radical Perfluoroalkylation/Cyclization Strategy To Access 2-Perfluoroalkylbenzothiazoles/Benzoselenazoles by EDA Complex

Journal

ORGANIC LETTERS
Volume 21, Issue 11, Pages 4019-4024

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01175

Keywords

-

Funding

  1. Centre of Advanced Analysis AMP
  2. Computational Science (Zhengzhou University)
  3. National Natural Science Foundation of China [21501010]
  4. Science and Technology Innovation Team in Henan Province [22120001]

Ask authors/readers for more resources

A novel and practical fluoroalkyl radical-initiated cascade reaction was developed to access diverse 2-fluoroalkylbenzothiazoles by reacting various fluoroalkyl radical sources, including perfluoroalkyl iodide (IC(n)F2(n+1), n = 3-8, 10), ICF(CF3)(2), ICF2COOEt, ICF2CF2Cl, or ICF2CF2Br, tetramethylethane-1,2-diamine (TMEDA), and 2-isocyanoaryl thioethers in tetrahydrofuran under nitrogen atmosphere and blue-light irradiation conditions. Furthermore, this one-pot protocol could well be expanded to access various 2-fluoroalkylbenzoselenazoles starting from (2-isocyanophenyl)(methyl)selane, perfluoroalkyl iodides (ICnF2n+1, n = 3-8) or ICF2COOEt and TMEDA.

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