Synthesis of 1-Difluoroalkylated Isoquinolines via Palladium-Catalyzed Radical Cascade Difluoroalkylation-Cyclization of Vinyl Isocyanides with Bromodifluoroacetic Derivatives

被引:19
作者
Liu, Yingle [1 ]
Zhang, Ke [2 ]
Jiang, Weidong [1 ]
Yang, Yi [1 ]
Jiang, Yan [1 ]
Liu, Xiaoqiang [1 ]
Xie, Ying [1 ]
Wu, Jincai [1 ]
Cai, Junjie [1 ]
Xu, Xiu-Hua [3 ]
机构
[1] Sichuan Univ Sci & Engn, Sch Chem & Environm Engn, 180 Xueyuan St, Zigong 643000, Sichuan, Peoples R China
[2] Donghua Univ, Coll Chem Chem Engn & Biotechnol, 2999 North Renmin Rd, Shanghai 201620, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
关键词
difluoroalkylation; gem-difluoromethylene; isoquinolines; palladium; radical reactions; C-H ETHOXYCARBONYLDIFLUOROMETHYLATION; INTERNAL ALKYNES; BOND ACTIVATION; RECENT PROGRESS; BORONIC ACIDS; LIGHT; ALKENES; FLUOROALKYLATION; ACCESS; DIFLUOROACETAMIDATION;
D O I
10.1002/asia.201601645
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A general method was developed for the synthesis of 1-difluoroalkyl isoquinolines via the palladium-catalyzed radical cascade difluoroalkylation-cyclization of vinyl isocyanides with bromodifluoroacetic derivatives. The difluoroalkylated cyclization products were readily converted to various other valuable gem-difluoro-containing compounds.
引用
收藏
页码:568 / 576
页数:9
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