Pd-PEPPSI: Pd-NHC Precatalyst for Suzuki-Miyaura Cross-Coupling Reactions of Amides

被引:108
|
作者
Lei, Peng [1 ,2 ]
Meng, Guangrong [2 ]
Ling, Yun [1 ]
An, Jie [1 ]
Szostak, Michal [2 ]
机构
[1] China Agr Univ, Coll Sci, Dept Appl Chem, Beijing 100193, Peoples R China
[2] Rutgers State Univ, Dept Chem, 73 Warren St, Newark, NJ 07102 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2017年 / 82卷 / 13期
关键词
N-HETEROCYCLIC CARBENES; BUCHWALD-HARTWIG; C CLEAVAGE; COMPLEXES; ACTIVATION; AMINATION; CATALYST; ANILINE; LIGANDS; IPENT;
D O I
10.1021/acs.joc.7b00749
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Pd-PEPPSI-IPr serves as a highly reactive precatalyst in the direct Suzuki-Miyaura cross-coupling of amides. An array of amides can be cross-coupled with a range of arylboronic acids in very good yields using a single, operationally simple protocol. The studies described represent the first use of versatile PEPPSI type of Pd-NHC complexes as catalysts for the cross-coupling of amides by N-C bond activation. The method is user-friendly, since it employs a commercially available, air- and moisture-stable Pd-PEPPSI-IPr complex. Pd-PEPPSI-IPr provides a significant improvement over all current Pd/phosphane catalysts for amide N-C bond activation. Mechanistic studies provide insight into the reaction rates of Pd-NHC-catalyzed cross-coupling of different amides, with Pd-PEPPSI-IPr being particularly effective for the cross-coupling of N-Boc carbamates under the developed conditions.
引用
收藏
页码:6638 / 6646
页数:9
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