112116-67-3Relevant academic research and scientific papers
Oxidative Trimerization of Amino Acids: Selective Synthesis of 2,3,5-Trisubstituted Pyridines
Xiang, Jia-Chen,Cheng, Yan,Wang, Zi-Xuan,Ma, Jin-Tian,Wang, Miao,Tang, Bo-Cheng,Wu, Yan-Dong,Wu, An-Xin
supporting information, p. 2997 - 3000 (2017/06/07)
An oxidative trimerization of three amino acids has been realized to furnish 2,3,5-trisubstuitued pyridines in both cross- and homo-trimerization types. This method is capable of converting simple linear biomass material to heterocycles, which features in
Cu-Catalyzed concise synthesis of pyridines and 2-(1 H)-pyridones from acetaldehydes and simple nitrogen donors
Li, Ziyuan,Huang, Xiaoqiang,Chen, Feng,Zhang, Chun,Wang, Xiaoyang,Jiao, Ning
supporting information, p. 584 - 587 (2015/03/04)
A highly selective copper-catalyzed concise synthesis of 3,5-diarylpyridine and 2-(1H)-pyridone has been achieved through cascade Chichibabin-type cyclization, C(sp3)-C(sp3) cleavage, and aerobic oxidation. Azide, ceric ammonium nitrate (CAN), and 2-aminopyridine are disclosed as efficient nitrogen donors in this Cu-catalysis using O2 as the oxidant. Water and molecular oxygen were employed as the oxygen source in the case of oxygenation.
