1238767-40-2Relevant academic research and scientific papers
An aerobic oxidative aza-[4+2] cycloaddition induced by radical cation salt: Synthesis of dihydroquinazoline derivatives
Luo, Liangliang,Zhao, Xiaolong,Zhang, Liang,Yuan, Yu,Lü, Shiwei,Jia, Xiaodong
supporting information, p. 5830 - 5833 (2016/12/03)
A facile and efficient radical cation salt-induced approach to dihydroquinazoline derivatives has been developed by sp3C[sbnd]H oxidation, and the method uses readily available glycine esters as the starting material under aerobic oxidation conditions without addition of any additive. The present method provides a convenient and practical route for construction of quinazoline skeleton.
Iron-catalyzed oxidative tandem reactions with TEMPO oxoammonium salts: Synthesis of dihydroquinazolines and quinolines
Rohlmann, Renate,Stopka, Tobias,Richter, Heinrich,Garcia Mancheno, Olga
, p. 6050 - 6064 (2013/07/26)
A straightforward iron-catalyzed divergent oxidative tandem synthesis of dihydroquinazolines and quinolines from N-alkylanilines using a TEMPO oxoammonium salt as a mild and nontoxic oxidant has been developed. Fe(OTf) 2 was the Lewis acid cata
A convenient synthesis of quinazoline derivatives via cascade imino-Diels-Alder and oxidation reaction
Chen, Xue Ming,Wei, Hui,Yin, Lu,Li, Xing Shu
experimental part, p. 782 - 786 (2011/11/12)
Quinazoline derivatives were synthesized from a-iminoesters via a cascade imino-Diels-Alder and then oxidation reaction catalyzed with CuBr2. This method provided a new strategy for preparing quinazoline derivatives which may be useful in the s
