Suzuki-Miyaura cross-coupling reaction of aryl chlorides with aryl boronic acids catalyzed by a palladium dichloride adduct of N-diphenylphosphanyl-2-aminopyridine

被引：24
|
作者：
Xu, Lin-Yan [1 ]
Liu, Chun-Yu [1 ]
Liu, Shi-Yuan [1 ]
Ren, Zhi-Gang [1 ,2 ]
Young, David James [3 ,4 ]
Lang, Jian-Ping [1 ,2 ]
机构：
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 210032, Peoples R China
[3] Monash Univ Malaysia, Sch Sci, Jalan Lagoon Selatan, Bandar Sunway 47500, Selangor Darul, Malaysia
[4] Univ Sunshine Coast, Fac Sci Hlth Educ & Engn, Maroochydore, Qld 4558, Australia
来源：
TETRAHEDRON | 2017年 / 73卷 / 22期
基金：
中国国家自然科学基金;
关键词：
Aryl chloride; Aryl boronic acid; Suzuki-Miyaura coupling; P-N donor ligand; Palladium(II); ROOM-TEMPERATURE; AQUEOUS-MEDIUM; C-C; STRUCTURAL-CHARACTERIZATION; ORGANOBORON COMPOUNDS; EFFICIENT CATALYSTS; ARYLBORONIC ACIDS; PHOSPHINE-LIGANDS; COMPLEXES; WATER;
D O I：
10.1016/j.tet.2017.04.034
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
One palladium dichloride adduct of a phosphine-pyridine ligand N-diphenylphosphanyl-2-aminopyridine (L-1) [(L-1)PdCl2] (1) has been prepared and structurally characterized. Compound 1 can be used as an effective catalyst for the Suzuki-Miyaura cross-coupling reactions of unreactive aryl chlorides with aryl boronic acids, and worked much better than its mono- or bidentate phosphine ligands. The reactions with a wide scope of substrates proceeded to give desired products in good to excellent yields. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码：3125 / 3132
页数：8
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