1532520-66-3Relevant academic research and scientific papers
Diethyl Azodicarboxylate-Promoted Oxidative [3 + 2] Cycloaddition for the Synthesis of Pyrrolo[2,1- a]isoquinolines
Xu, Ya-Wen,Wang, Jiankun,Wang, Guangji,Zhen, Le
, p. 91 - 102 (2021)
A novel metal-free protocol for the effective and efficient construction of pyrrolo[2,1-a]isoquinolines via a diethyl azodicarboxylate (DEAD)-promoted oxidative [3 + 2] cycloaddition/aromatization tandem reaction is described. Instead of the reported two-
A general, simple and green process to access pyrrolo[2,1-a]isoquinolines using a KI/TBHP catalytic system
Huang, Huan-Ming,Huang, Fang,Li, Yu-Jin,Jia, Jian-Hong,Ye, Qing,Han, Liang,Gao, Jian-Rong
, p. 27250 - 27258 (2014/07/21)
A novel KI/TBHP-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade reaction provided general, efficient and green access to biologically important pyrrolo[2,1-a]isoquinolines. The product pyrrolo[2,1-a]isoquinolines were obtained from rea
Iodine-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade with hydrogen peroxide as the terminal oxidant: General route to pyrrolo[2,1- a ]isoquinolines
Huang, Huan-Ming,Li, Yu-Jin,Ye, Qing,Yu, Wu-Bin,Han, Liang,Jia, Jian-Hong,Gao, Jian-Rong
, p. 1084 - 1092 (2014/03/21)
We report a novel molecular iodine-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade process with hydrogen peroxide as the terminal oxidant for the construction of pyrrolo[2,1-a]isoquinolines. The product pyrrolo[2,1-a]isoquinolines were
