Ir-catalyzed highly selective addition of pyridyl C-H bonds to aldehydes promoted by triethylsilane

被引:140
作者
Li, Bi-Jie [1 ,2 ,3 ]
Shi, Zhang-Jie [1 ,2 ,3 ,4 ]
机构
[1] Peking Univ, BNLMS, Beijing 100871, Peoples R China
[2] Peking Univ, Key Lab Bioorgan Chem & Mol Engn, Minist Educ, Coll Chem, Beijing 100871, Peoples R China
[3] Peking Univ, Green Chem Ctr, Beijing 100871, Peoples R China
[4] Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
关键词
INTERMOLECULAR DIRECT ARYLATION; DIRECTED ORTHO-METALATION; CARBON-HYDROGEN; HETEROAROMATIC-COMPOUNDS; UNSATURATED MOLECULES; AROMATIC HETEROCYCLES; IRIDIUM COMPLEXES; COUPLING REACTION; ARYL HALIDES; N-OXIDES;
D O I
10.1039/c0sc00419g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report herein an iridium-catalyzed activation of pyridine C-H bond and its nucleophilic addition to benzaldehydes. The reaction was applicable to various pyridine derivatives and aryl aldehydes. In contrast to most methods that selectively functionalize the C2 pyridine C-H bond, this reaction proceeded with unusual meta-selectivity. An independently synthesized silyl iridium complex was able to catalyze the reaction, indicating that a silyl iridium intermediate might be responsible for the novel reactivity and the unusual selectivity.
引用
收藏
页码:488 / 493
页数:6
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