Palladium-Catalyzed C-H Activation/Cross-Coupling of Pyridine N-Oxides with Nonactivated Secondary Alkyl Bromides

被引:221
|
作者
Xiao, Bin [1 ,2 ,3 ]
Liu, Zhao-Jing [1 ]
Liu, Lei [2 ,3 ]
Fu, Yao [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei 230026, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[3] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
基金
中国博士后科学基金;
关键词
SUZUKI CROSS-COUPLINGS; ARYL BOND FORMATION; HECK-TYPE REACTIONS; DIRECT ARYLATION; FUNCTIONALIZATION; CHLORIDES; LIGANDS; HALIDES; 2-ALKYLATION; DISCOVERY;
D O I
10.1021/ja3113752
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An unexpected C-H activation/C-C cross-coupling reaction has been found to occur between pyridine N-oxides and general nonactivated secondary and even tertiary alkyl bromides. It provides a practically useful approach for the synthesis of alkylated pyridine derivatives. Experimental observations indicated that the C-Br cleavage step involves a radical-type process. Thus, the title reaction provides a rather extraordinary example of Pd-catalyzed cross-coupling of secondary and tertiary aliphatic electrophiles.
引用
收藏
页码:616 / 619
页数:4
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