Synthesis of N-heterocyclic carbene-PdCl2-(iso)quinoline complexes and their application in arylamination at low catalyst loadings

被引:32
作者
Liu, Feng [1 ]
Zhu, Yi-Ran [1 ]
Song, Lu-Gan [1 ]
Lu, Jian-Mei [1 ]
机构
[1] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
CROSS-COUPLING REACTIONS; BUCHWALD-HARTWIG AMINATION; TEMPERATURE SUZUKI-MIYAURA; ARYL CHLORIDES; C-N; ARYLBORONIC ACIDS; BOND FORMATION; VERSATILE CATALYST; EFFICIENT CATALYST; CARBENE LIGANDS;
D O I
10.1039/c6ob00013d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new type of N-heterocyclic carbene-PdCl2-(iso)quinoline complexes 3 were successfully achieved in acceptable to good yields from easily available starting materials under mild conditions, and their structures were unambiguously confirmed using X-ray single crystal diffraction. Furthermore, their catalytic activity toward Buchwald-Hartwig arylamination of aryl chlorides with primary and secondary amines was fully tested. Under the optimal reaction conditions, the expected arylated amines can be obtained in high to excellent yields at low catalyst loadings (0.005-0.05 mol%). It may be worth noting here that comparison of these complexes with other well-defined and easily available NHC-Pd(II) complexes bearing different N-containing ancillary ligands was also carried out, showing their superior catalytic activity over all others.
引用
收藏
页码:2563 / 2571
页数:9
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