Design, synthesis and application of triazole ligands in suzuki miyaura cross coupling reaction of aryl chlorides

2020 ◽  
Vol 1206 ◽  
pp. 127753 ◽  
Author(s):  
Sobia Jabeen ◽  
Rasheed Ahmad Khera ◽  
Javed Iqbal ◽  
Muhammad Asgher
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Design Synthesis ◽  
Aryl Chlorides ◽  
Cross Coupling Reaction

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
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Aryl Chlorides ◽  
Cross Coupling Reaction

Suzuki-Miyaura Cross-Coupling Towards 4-Amino Biphenyl Intermediates

2019 ◽  
Author(s):  
Tomasz Jastrząbek ◽  
Artur Ulikowski ◽  
Rafał Lisiak
Keyword(s):  
Chemical Industry ◽  
Short Communication ◽  
Phenylboronic Acid ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Amino Groups ◽  
Aryl Chlorides ◽  
Cross Coupling Reaction ◽  
Direct Cross

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>

Room temperature Stille cross-coupling reaction of unreactive aryl chlorides and heteroaryl chlorides

2010 ◽  
Vol 46 (3) ◽  
pp. 478-480 ◽  
Author(s):  
Dong-Hwan Lee ◽  
Abu Taher ◽  
Wha-Seung Ahn ◽  
Myung-Jong Jin
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Aryl Chlorides ◽  
Cross Coupling Reaction
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