scholarly journals Palladium-Catalyzed Borylation of Primary Alkyl Bromides

2012 ◽  
Vol 77 (15) ◽  
pp. 6629-6633 ◽  
Author(s):  
Amruta Joshi-Pangu ◽  
Xinghua Ma ◽  
Mohamed Diane ◽  
Sidra Iqbal ◽  
Robert J. Kribs ◽  
...  
2017 ◽  
Vol 139 (33) ◽  
pp. 11595-11600 ◽  
Author(s):  
Alexander R. O. Venning ◽  
Megan R. Kwiatkowski ◽  
Joan E. Roque Peña ◽  
Brendan C. Lainhart ◽  
Akil A. Guruparan ◽  
...  

2017 ◽  
Vol 13 ◽  
pp. 2610-2616 ◽  
Author(s):  
Tao Fan ◽  
Wei-Dong Meng ◽  
Xingang Zhang

An efficient palladium-catalyzed Heck-type reaction of secondary trifluoromethylated alkyl bromides has been developed. The reaction proceeds under mild reaction conditions with high efficiency and excellent functional group tolerance, even towards formyl and hydroxy groups. Preliminary mechanistic studies reveal that a secondary trifluoromethylated alkyl radical is involved in the reaction.


2017 ◽  
Vol 56 (49) ◽  
pp. 15683-15687 ◽  
Author(s):  
Wen-Jun Zhou ◽  
Guang-Mei Cao ◽  
Guo Shen ◽  
Xing-Yong Zhu ◽  
Yong-Yuan Gui ◽  
...  

Synthesis ◽  
2018 ◽  
Vol 50 (15) ◽  
pp. 2908-2914 ◽  
Author(s):  
Rui Shang ◽  
Yao Fu ◽  
Guang-Zu Wang

A palladium catalyst in combination with two types of phosphine ligands efficiently catalyzes direct C–H alkylation of heteroarenes with secondary and tertiary alkyl bromides under irradiation conditions. Irradiation of blue light-emitting diodes (blue LEDs) effectively excites phosphine-ligated palladium catalyst to facilitate oxidative addition with alkyl bromides, and also excites the alkylpalladium species to enable the generation of alkyl radicals to react with heteroarenes.


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