Transition metal-catalyzed C-H activation/annulation approaches to isoindolo[2,1-b]isoquinolin-5(7H)-ones

被引:7
作者
Tang, Xiao [1 ]
Ding, Songtao [1 ]
Song, Liangliang [2 ]
Van der Eycken, Erik V. [3 ,4 ]
机构
[1] Nanjing Forestry Univ, Coll Sci, Nanjing 210037, Peoples R China
[2] Nanjing Forestry Univ, Coll Chem Engn, Jiangsu Coinnovat Ctr Efficient Proc & Utilizat Fo, Int Innovat Ctr Forest Chem & Mat,Jiangsu Prov Key, Nanjing 210037, Jiangsu, Peoples R China
[3] Katholieke Univ Leuven, Univ Leuven, Dept Chem, Lab Organ & Microwave Assisted Chem LOMAC, Celestijnenlaan 200F, B-3001 Leuven, Belgium
[4] RUDN Univ, Peoples Friendship Univ Russia, Miklukho Maklaya St 6, Moscow 117198, Russia
关键词
transition metal; C-H activation; annulation; isoindolo[2; 1-b]isoquinolin-5(7H)-one; NH ISOQUINOLONES; TOPOISOMERASE-I; DIRECTING GROUP; BOND-CLEAVAGE; ACTIVATION; CYCLIZATION; CAMPTOTHECIN; ROSETTACIN; ALKYNES; CYCLOCARBONYLATION;
D O I
10.1002/tcr.202200255
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The isoindolo[2,1-b]isoquinolin-5(7H)-one scaffold is widely present in lots of bioactive natural products. Diverse types of strategies have been developed to construct this scaffold. Recently, transition metal-catalyzed C-H activation/annulation is emerging as a powerful and straightforward method to construct diverse polyheterocycles with high atom- and step-economy. It also has been employed for the synthesis of the isoindolo[2,1-b]isoquinolin-5(7H)-one scaffold. This review provides an introduction to recent advances for the preparation of isoindolo[2,1-b]isoquinolin-5(7H)-ones by using transition metal-catalyzed C-H activation/annulation. It will help researchers to find hidden opportunities and accelerate the discovery of novel transformations based on C-H activation/annulation.
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页数:15
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