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Palladium-Catalyzed C-H Activation/Cross-Coupling of Pyridine N-Oxides with Nonactivated Secondary Alkyl Bromides
被引:222
|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.
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页码:616 / 619
页数:4
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