Facile synthesis of aryl(het)cyclopropane catalyzed by palladacycle

被引:20
作者
Zhang, Min [1 ]
Cui, Xiuling [1 ]
Chen, Xiaopei [1 ]
Wang, Lianhui [1 ,2 ]
Li, Jingya [2 ]
Wu, Yusheng [2 ]
Hou, Lifen [1 ]
Wu, Yangjie [1 ]
机构
[1] Zhengzhou Univ, Dept Chem, Key Lab Appl Chem Henan Univ, Henan Key Lab Chem Biol & Organ Chem, Zhengzhou 450052, Peoples R China
[2] Tetranov Biopharm Inc, Zhengzhou 450052, Peoples R China
关键词
Palladacycle; Suzuki cross-coupling; Cyclopropylboronic acid; Arylcyclopropane; CROSS-COUPLING REACTIONS; CYCLOPROPYLBORONIC ACID; ARYL HALIDES; CYCLOPALLADATED FERROCENYLIMINE; DERIVATIVES; CYCLOPROPANES; ALKYNES;
D O I
10.1016/j.tet.2011.11.024
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Sphos (2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl) adduct of cyclopalladated ferrocenylimine (Ile) exhibited highly catalytic activity for the Suzuki cross-coupling reaction of cyclopropylboronic acid with aryl(het) halides with 1 mol % catalyst loading. This process was applied to both of aryl and heteroaryl halides (Br and Cl), and made the various arylcyclopropane and heteroarylcyclopropane to be easily synthesized. A variety of substituents on the aryl halides, such as alkyl, acetyl, benzoyl, ether, formyl, carboxylate, methoxy, nitro and cyano were tolerated. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:900 / 905
页数:6
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