Nickel-Catalyzed Reductive Coupling of Aryl Halides with Secondary Alkyl Bromides and Allylic Acetate
Shulin Wang, Qun Qian and Hegui Gong*
*Department of Chemistry, Shanghai University, 99 Shang-Da
Road, Shanghai 200444, China, Email: hegui_gong
shu.edu.cn
S. Wang, Q. Qian, H. Gong, Org. Lett., 2012, 14, 3352-3355.
DOI: 10.1021/ol3013342
see article for more reactions
Abstract
A room-temperature Ni-catalyzed reductive coupling of aryl bromides with secondary alkyl bromides provides products in good to excellent yields. Slight modification of this protocol allows efficient coupling of activated aryl chlorides with cyclohexyl bromide and aryl bromides with allylic acetate.
see article for more examples
Key Words
ID: J54-Y2012-2190
