A practical synthesis of benzothiophenes via visible-light-promoted cyclization of disulfides and alkynes

2017 ◽  
Vol 15 (3) ◽  
pp. 550-554 ◽  
Author(s):  
Lin-Miao Ye ◽  
Lu Qian ◽  
Yan-Yan Chen ◽  
Xue-Jing Zhang ◽  
Ming Yan

Visible-light-promoted radical cyclization of disulfides and alkynes provided benzothiophenes in good yields.

2016 ◽  
Vol 18 (5) ◽  
pp. 1004-1007 ◽  
Author(s):  
Tiebo Xiao ◽  
Linyong Li ◽  
Yang Xie ◽  
Zong-Wan Mao ◽  
Lei Zhou

2019 ◽  
Vol 21 (12) ◽  
pp. 3362-3369 ◽  
Author(s):  
Long Zou ◽  
Pinhua Li ◽  
Bin Wang ◽  
Lei Wang

An efficient strategy for the preparation of trifluoromethylated dihydroisoquinolinones via visible-light induced radical cyclization of N-allylbenzamides with CF3SO2Na was developed.


2015 ◽  
Vol 51 (70) ◽  
pp. 13508-13510 ◽  
Author(s):  
Chuanhua Qu ◽  
Pan Xu ◽  
Wujiang Ma ◽  
Yixiang Cheng ◽  
Chengjian Zhu

A novel visible light mediated cyclization of enol lactones with difluoroacyl arenes via a free radical tandem difluoroalkylation and C–C coupling of butenolides is presented. This strategy provides a facile approach to potential biological fluorinated γ-butyrolactones with excellent diastereoselectivity.


2020 ◽  
Vol 1 (1) ◽  
pp. 42-51 ◽  
Author(s):  
Pengzi Wang ◽  
Quanqing Zhao ◽  
Wenjing Xiao ◽  
Jiarong Chen

2020 ◽  
Vol 85 (4) ◽  
pp. 2385-2394 ◽  
Author(s):  
Yu Liu ◽  
Zan Chen ◽  
Qiao-Lin Wang ◽  
Pu Chen ◽  
Jun Xie ◽  
...  

Synthesis ◽  
2021 ◽  
Author(s):  
Devaiah Vytla ◽  
Kumargurubaran Kaliyaperumal ◽  
Rajeswari Velayuthaperumal ◽  
Parinita Shaw ◽  
Raj Gautam ◽  
...  

AbstractA photocatalyzed and highly efficient trifluoromethylation of N-arylvinylsulfonamides using commercially available CF3SO2Cl as the trifluoromethyl radical source under blue LEDs is reported. The reaction proceeds through radical cyclization under mild conditions. An investigation of the substrate scope is performed to establish a general, synthetically useful protocol for the synthesis of novel trifluoromethylated 1,3-dihydrobenzo[c]isothiazole 2,2-dioxides in moderate to high yields. This method is also successfully applied for the synthesis of difluoromethylated and trifluoroethylated 1,3-dihydrobenzo[c]isothiazole 2,2-dioxides in good to excellent yields.


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