Cross-Coupling Reactions of Aryl Chlorides with Organochlorosilanes:  Highly Effective Methods for Arylation or Alkenylation of Aryl Chlorides

1996 ◽  
Vol 61 (21) ◽  
pp. 7232-7233 ◽  
Author(s):  
Ken-ichi Gouda ◽  
Emiko Hagiwara ◽  
Yasuo Hatanaka ◽  
Tamejiro Hiyama
2009 ◽  
Vol 87 (1) ◽  
pp. 171-175 ◽  
Author(s):  
Daniele Vinci ◽  
Nelson Martins ◽  
Ourida Saidi ◽  
John Bacsa ◽  
Amadeu Brigas ◽  
...  

A series of ferrocenyl oxazaphospholidine phosphines that differ electronically and sterically were investigated as ligands for the Suzuki–Miyaura cross-coupling reactions. One of these compounds, 1, was shown to be highly effective in the coupling reactions of bulky aryl bromides with boronic acids when combined with Pd(OAc)2, while another, 2, was capable of coupling aryl chlorides with boronic acids. However, these ligands were less effective in asymmetric induction.Key words: Suzuki–Miyaura coupling, ferrocenyl phosphines, aryl bromides, aryl chlorides, palladium.


2014 ◽  
Vol 136 (40) ◽  
pp. 14027-14030 ◽  
Author(s):  
Ling Li ◽  
Shibin Zhao ◽  
Amruta Joshi-Pangu ◽  
Mohamed Diane ◽  
Mark R. Biscoe

ChemInform ◽  
2015 ◽  
Vol 46 (16) ◽  
pp. no-no
Author(s):  
Ling Li ◽  
Shibin Zhao ◽  
Amruta Joshi-Pangu ◽  
Mohamed Diane ◽  
Mark R. Biscoe

2017 ◽  
Vol 41 (1) ◽  
pp. 372-376 ◽  
Author(s):  
Jinyi Song ◽  
Hongyan Zhao ◽  
Yang Liu ◽  
Huatao Han ◽  
Zhuofei Li ◽  
...  

A series of N,O-bidentate ligands were synthesized and studied as high activity ligands for palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl chlorides with arylboronic acids under mild conditions.


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