Chemoselective aerobic oxidation of 2-amino-N-benzylanilines into N-(2-aminophenyl)imines via a nitroxide-free copper catalysis
-
Add time:08/22/2019 Source:sciencedirect.com
Chemoselective oxidative synthesis of N-(2-aminophenyl)imines from 2-amino-N-benzylanilines was accomplished through combined use of O2(air) and copper salt. This transformation was performed at room temperature, and the mild oxidation was efficient and chemoselective without using nitroxyl radicals and ligands.
We also recommend Trading Suppliers and Manufacturers of N(2)-ethylguanine (cas 19545-00-7). Pls Click Website Link as below: cas 19545-00-7 suppliers
Prev:Spin-probe ESR and molecular modeling studies on calcium carbonate dispersions in overbased detergent additives
Next:A convenient synthesis of 2-acyl benzothiazoles/thiazoles from benzothiazole/thiazole and N,N'-carbonyldiimidazole activated carboxylic acids) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Data ArticleThermodynamic, DFT and molecular dynamics studies of intermolecular interactions between 2-methoxyaniline and N- substituted amide mixtures08/26/2019
- Production of N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid by BMED process using porous P84 co-polyimide membranes08/25/2019
- On the geometry of tensor network states of 2 × N grids08/24/2019
- A convenient synthesis of 2-acyl benzothiazoles/thiazoles from benzothiazole/thiazole and N,N'-carbonyldiimidazole activated carboxylic acids08/23/2019
