Derivation of Benzothiadiazine-1,1-dioxide Scaffolds via Transition Metal-Catalyzed C-H Activation/Annulation

被引:6
|
作者
Lai, Ruizhi [1 ,2 ]
Xu, Shuran [1 ,2 ]
Zhang, Qingyao [1 ,2 ]
Zhou, Hui [1 ,2 ]
Luo, Cankun [1 ,2 ]
Wang, Yuerong [1 ,2 ]
Hai, Li [1 ,2 ]
Wu, Yong [1 ,2 ]
机构
[1] Sichuan Univ, Sichuan Engn Lab Plant Sourced Drug, West China Sch Pharm, Key Lab Drug Targeting & Drug Delivery Syst,Educ M, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, Sichuan Res Ctr Drug Precis Ind Technol, Chengdu 610041, Sichuan, Peoples R China
来源
CHINESE JOURNAL OF CHEMISTRY | 2023年 / 41卷 / 16期
关键词
C-H activation; Annulation; Ruthenium; Rhodium; Heterocycles; Fused-ring systems; Spiro compounds; Diazo compounds; CONSTRUCTION; 1,1-DIOXIDES; STRATEGY; TANDEM;
D O I
10.1002/cjoc.202300095
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Comprehensive SummaryBenzothiadiazine-1,1-dioxide scaffold is bioactive framework with wild utility and applications. Synthesis of benzothiadiazine-fused isoquinoline derivatives and spiro benzothiadiazine derivatives through transition metal-catalyzed C-H activation/annulation was reported. 3-Phenyl-2H-benzothiadiazine-1,1-dioxide was used as the reaction substrate, and vinylene carbonate and 4-diazopyrazolone were used as the coupling reagents, respectively. This strategy provides straightforward access to complex N-heterocycles in a highly efficient and simple manner.
引用
收藏
页码:1973 / 1978
页数:6
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