Palladacycle-catalyzed Suzuki-Miyaura reaction of aryl/heteroaryl halides with MIDA boronates in EtOH/H2O or H2O

被引：10

作者：

Li, Yabo ^{[1
]}

Wang, Jingran ^{[1
]}

Wang, Zhiwei ^{[1
]}

Huang, Mengmeng ^{[1
]}

Yan, Beiqi ^{[1
]}

Cui, Xiuling ^{[1
]}

Wu, Yusheng ^{[1
,2
]}

Wu, Yangjie ^{[1
]}

机构：

[1] Zhengzhou Univ, Coll Chem & Mol Engn, Henan Key Lab Chem Biol & Organ Chem, Key Lab Appl Chem Henan Univ, Zhengzhou 450052, Peoples R China

[2] Tetranov Biopharm LLC, Zhengzhou 450052, Peoples R China

来源：

RSC ADVANCES | 2014年 / 4卷 / 68期

基金：

中国国家自然科学基金;

关键词：

CROSS-COUPLING REACTION; BORONIC ACIDS; ARYL CHLORIDES; PALLADIUM; EFFICIENT; COMPLEX;

D O I：

10.1039/c4ra07486f

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

With good to excellent yields, a series of mono- or diheteroaryl compounds were synthesized via the palladacycle-catalyzed Suzuki-Miyaura reaction of various N-methyliminodiacetic acid (MIDA) boronates with aryl/heteroaryl halides in EtOH/H2O or H2O.

引用

页码：36262 / 36266

页数：5

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