Nickel-catalysed cross-coupling reaction of aryl(trialkyl)silanes with aryl chlorides and tosylates

2011 ◽  
Vol 47 (1) ◽  
pp. 307-309 ◽  
Author(s):  
Shi Tang ◽  
Masahide Takeda ◽  
Yoshiaki Nakao ◽  
Tamejiro Hiyama
2019 ◽  
Author(s):  
Tomasz Jastrząbek ◽  
Artur Ulikowski ◽  
Rafał Lisiak

The preparation of biphenyl derivatives bearing amino groups via direct cross-coupling reaction is being widely explored due to its importance for many branches of the chemical industry. One of the necessary components for such a transformation are halogenated arenes. In order to make the process more economical, we focus on inexpensive and easily available aryl chlorides which usually are not considered reagents of choice for catalytic couplings. In the following short communication, we report the results of the coupling of relatively unreactive chloroaniline with a fluorinated phenylboronic acid leading to the corresponding aminobiphenyl.<br>


2010 ◽  
Vol 46 (3) ◽  
pp. 478-480 ◽  
Author(s):  
Dong-Hwan Lee ◽  
Abu Taher ◽  
Wha-Seung Ahn ◽  
Myung-Jong Jin

2018 ◽  
Vol 1134 ◽  
pp. 1-7 ◽  
Author(s):  
Khalil Ahmad ◽  
Bilal Ahmad Khan ◽  
Bilal Akram ◽  
Jahanzeb Khan ◽  
Rashid Mahmood ◽  
...  

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