Indium-mediated Coupling Reaction of Sulfonyl Chlorides with Alkyl Bromides in Water. A Facile Synthesis of Sulfones

1998 ◽  
pp. 588-589 ◽  
Author(s):  
Lei Wang ◽  
Yongmin Zhang
2016 ◽  
Vol 1 (15) ◽  
pp. 4721-4725 ◽  
Author(s):  
Bhaskaran Savitha ◽  
Ayyiliath M. Sajith ◽  
Eeda Koti Reddy ◽  
C. S. Ananda Kumar ◽  
M. Syed Ali Padusha

1976 ◽  
Vol 54 (3) ◽  
pp. 498-499 ◽  
Author(s):  
Richard F. Langler

Benzylic sulfides have been shown to furnish sulfonyl chlorides in excellent yields, upon reaction with molecular chlorine in aqueous acetic acid. The reaction most likely proceeds through the intermediacy of the corresponding sulfenyl chloride.


2020 ◽  
Vol 484 ◽  
pp. 110726 ◽  
Author(s):  
Xin Ge ◽  
Meng Ge ◽  
Xinzhi Chen ◽  
Chao Qian ◽  
Xuemin Liu ◽  
...  

2019 ◽  
Vol 55 (69) ◽  
pp. 10265-10268 ◽  
Author(s):  
Yao Zhou ◽  
Ya Wang ◽  
Yixian Lou ◽  
Qiuling Song

The first example of denitrogenative radical coupling with 3-aminoindazoles is presented. A diverse array of 1,2-thiobenzonitriles were obtained in good yields with wide substrate scope via oxidative C–N cleavage of 3-aminoindazoles.


2014 ◽  
Vol 50 (45) ◽  
pp. 5993-5996 ◽  
Author(s):  
Takashi Kippo ◽  
Ilhyong Ryu

A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields.


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