1073486-93-7Relevant articles and documents
Nickel-Catalyzed Annulation of o-Haloarylamidines with Aryl Acetylenes: Synthesis of Isoquinolone and 1-Aminoisoquinoline Derivatives
Xie, Hao,Xing, Qiaoyan,Shan, Zhifei,Xiao, Fuhong,Deng, Guo-Jun
, p. 1896 - 1901 (2019/03/07)
An efficient method for the synthesis of substituted 1(2H)-isoquinolone derivatives via nickel-catalyzed annulation of substituted 2-halobenzamidines with aryl alkynes in the presence of water is described. Benzo[4,5]imidazo[2,1-a]isoquinolines were formed as the dominated products when dry dimethyl sulfoxide was used as the solvent. Furthermore, when benzyl substituted amidines were used as the substrates, debenzylation reaction occured to provide various 1-aminoisoquinoline products. (Figure presented.).
Palladium-catalyzed carbonylation-decarboxylation of diethyl(2-iodoaryl) malonates with imidoyl chlorides: An efficient route to substituted isoquinolin-1(2H)-ones
Zheng, Zhaoyan,Alper, Howard
supporting information; experimental part, p. 4903 - 4906 (2009/05/07)
(Chemical Equation Presented) A wide variety of substituted isoquinolin-1(2H)-ones were synthesized in reasonable to good yields by the palladium-catalyzed cyclization of diethyl(2-iodoaryl)malonates with imidoyl chlorides and carbon monoxide in tetrahydrofuran. A palladium-catalyzed carbonylation-decarboxylation process may be involved in the one-step synthesis of the isoquinolin-1(2H)-ones.