Iron-catalyzed synthesis of arylsulfinates through radical coupling reaction

2016 ◽  
Vol 52 (14) ◽  
pp. 2980-2983 ◽  
Author(s):  
Weixi Zhang ◽  
Meiming Luo

A novel iron-catalyzed synthesis of arylsulfinates from diaryliodonium salts and rongalite through radical coupling reaction is described. Desired products can be prepared in good yields in air at room temperature in 20 minutes without the need for any ligands and additives.

2020 ◽  
Vol 22 (2) ◽  
pp. 336-341 ◽  
Author(s):  
Shulei Pan ◽  
Min Jiang ◽  
Jinjin Hu ◽  
Ruigang Xu ◽  
Xiaofei Zeng ◽  
...  

A general and efficient visible-light photoredox-catalyzed decarboxylative radical coupling reaction of N-aryl amino acids with aldehydes or ketones for the synthesis of 1,2-amino alcohols in water at room temperature is described.


2017 ◽  
Vol 359 (20) ◽  
pp. 3551-3554 ◽  
Author(s):  
Wen-Ting Wei ◽  
Wen-Ming Zhu ◽  
Wei-Wei Ying ◽  
Yi-Ning Wang ◽  
Wen-Hui Bao ◽  
...  

2021 ◽  
Vol 23 (2) ◽  
pp. 774-779
Author(s):  
Pengfei Niu ◽  
Jingya Yang ◽  
Yong Yuan ◽  
Yongxin Zhang ◽  
Chenxing Zhou ◽  
...  

A redox-neutral decarboxylative radical–radical coupling reaction of heteroaryl methylamines with NHPI esters has been developed by employing a copper complex as a photocatalyst with blue LED irradiation.


Synlett ◽  
2017 ◽  
Vol 28 (16) ◽  
pp. 2153-2156 ◽  
Author(s):  
Wen-Ting Wei ◽  
Hongze Liang ◽  
Wen-Ming Zhu ◽  
Weida Liang ◽  
Yi Wu ◽  
...  

A radical–radical cross-coupling reaction of phenols with tert-butyl nitrite has been developed with the use of water as an additive. This method allows the construction of C–N bonds under an air atmosphere at room temperature, providing the ortho-nitrated phenol derivative in moderate to good yields.


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