An efficient synthesis of 2-trifluoromethyl quinolines via gold-catalyzed cyclization of trifluoromethylated propargylamines
-
Add time:09/10/2019 Source:sciencedirect.com
A highly efficient cyclization reaction of trifluoromethylated propargylamines leading to 2-trifluoromethyl-4-aryl quinolines was developed by using gold(I) as a catalyst under extremely mild conditions.
We also recommend Trading Suppliers and Manufacturers of 4-CHLORO-2-METHYL-7-(TRIFLUOROMETHYL)QUINOLINE (cas 18529-09-4). Pls Click Website Link as below: cas 18529-09-4 suppliers
Prev:Facilely accessible quinoline derivatives as potent antibacterial agents
Next:Observation of ψ(3686)→η′e+e−) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Facilely accessible quinoline derivatives as potent antibacterial agents09/09/2019
- C5-selective trifluoromethylation of 8-amino quinolines via photoredox catalysis09/08/2019
- 3-Substituted Quinolines as RORγt Inverse Agonists09/07/2019
- Design, Synthesis and Anticancer Evaluation of New Substituted Thiophene-Quinoline Derivatives09/06/2019
- Short communication2,8-bis(trifluoromethyl)quinoline analogs show improved anti-Zika virus activity, compared to mefloquine09/05/2019


