1287736-93-9Relevant 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
Synthesis of Polysubstituted Imidazoles and Pyridines via Samarium(III) Triflate-Catalyzed [2+2+1] and [4+2] Annulations of Unactivated Aromatic Alkenes with Azides
Wang, Yingchun,Li, Jiuling,He, Yan,Xie, Yuyang,Wang, Hengshan,Pan, Yingming
, p. 3229 - 3241 (2015/11/03)
Samarium(III) triflate-catalyzed [2+2+1] and [4+2] annulations have been identified for the preparation of fully substituted imidazoles and 2,3,5-trisubstituted pyridines from the readily available unactivated aromatic alkenes and azidomethyl aromatics. T
A metal-free decarboxylative cyclization from natural α-amino acids to construct pyridine derivatives
Wang, Qiang,Wan, Changfeng,Gu, Yang,Zhang, Jintang,Gao, Lingfeng,Wang, Zhiyong
supporting information; experimental part, p. 578 - 581 (2011/05/06)
A metal-free decarboxylative cyclization from natural α-amino acids was developed and applied in the preparation of pyridine derivatives. By virtue of this method, a series of pyridines containing the moiety of natural α-amino acids can be synthesized efficiently from the corresponding natural α-amino acids. The Royal Society of Chemistry.
