Visible-light-induced direct perfluoroalkylation/heteroarylation of [1.1.1]propellane to diverse bicyclo[1.1.1]pentanes (BCPs) under metal and photocatalyst-free conditions

被引:61
|
作者
Zhu, Jiashun [1 ]
Guo, Yirui [1 ]
Zhang, Yuru [1 ]
Li, Wanmei [1 ]
Zhang, Pengfei [1 ]
Xu, Jun [1 ]
机构
[1] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 311121, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOCHEMICAL ACTIVITY; ALPHA-ALKYLATION; QUINOXALIN-2(1H)-ONES; CATALYSIS; DRIVEN; PHOSPHONATION; FLUORINATION; CHEMISTRY; ELECTRON; DRUG;
D O I
10.1039/d2gc04521d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, a green and novel multi-component reaction for direct perfluoroalkylation/heteroarylation of [1.1.1]propellane with heteroarenes and perfluoroalkyl iodines has been described. This transformation is facilitated by visible light in the absence of any transition-metal catalysts and photocatalysts. Various heteroarenes and perfluoroalkyl iodines are well compatible, providing the corresponding products in moderate-to-good yields. The control experiments demonstrate that a radical-relay mechanism is responsible for the cascade reaction. Such a methodology offers an efficient and practical access to diverse 1-perfluoroalkyl-3-heteroaryl bicyclo[1.1.1]pentanes (BCPs) with the potential for various applications in organic synthesis.
引用
收藏
页码:986 / 992
页数:7
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