Affiliation:
1. Department of Pharmaceutical and Biological Engineering, School of Chemical Engineering, Sichuan University
2. State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University
Abstract
A concise and efficient aerobic oxidation and oxygenation approach for the construction of 2-aroylquinolines has been developed through copper-catalyzed annulation of anilines, acetaldehydes, and dioxygen. 2,2,6,6-Tetramethylpiperidine-1-oxyl was employed to direct the selectivity toward the desired 2-aroyl products. Molecular oxygen was used in this transformation as an environmentally benign source of oxygen.
Funder
National Basic Research Program of China
Peking University Health Science Center
National Young Top-Notch Talent Support Program
Fundamental Research Funds for the Central Universities
National Natural Science Foundation of China
Cited by
10 articles.
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