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

页码：3125 / 3132

页数：8

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