An active catalytic system for Suzuki-Miyaura cross-coupling reactions using low levels of palladium loading

被引：0

作者：

Yan M.-Q. ^{[1
]}

Yuan J. ^{[1
,2
]}

Lan F. ^{[1
]}

Zeng S.-H. ^{[1
]}

Gao M.-Y. ^{[1
]}

Liu S.-H. ^{[1
]}

Chen J. ^{[1
,2
]}

Yu G.-A. ^{[1
,2
]}

机构：

[1] Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, Central China Normal University, Wuhan

[2] Chemical Biology Center, College of Chemistry, Central China Normal University, Wuhan

来源：

| 1600年 / Royal Society of Chemistry卷 / 15期

基金：

中国国家自然科学基金;

关键词：

Chlorine compounds;

D O I：

10.1039/c7ob00178a

中图分类号：

学科分类号：

摘要：

An easily available Pd(OAc)2/(2-(anthracen-9-yl)-1H-inden-3-yl) dicyclohexylphosphine/toluene/iPrOH/water catalytic system was developed, which shows high catalytic activity in the Suzuki-Miyaura cross-coupling reactions of a diverse array of aryl and heteroaryl chlorides with Pd loadings down to 0.01 mol%. © The Royal Society of Chemistry 2017.

引用

页码：3924 / 3929

页数：5

共 50 条

[1] An active catalytic system for Suzuki Miyaura cross-coupling reactions using low levels of palladium loading
Yan, Meng-Qi
Yuan, Jia
Lan, Fang
Zeng, Si-Hao
Gao, Meng-Yue
Liu, Sheng-Hua
Chen, Jian
Yu, Guang-Ao
ORGANIC & BIOMOLECULAR CHEMISTRY, 2017, 15 (18) : 3924 - 3929
[2] Palladium Supported on Silk Fibroin for Suzuki-Miyaura Cross-Coupling Reactions
Rizzo, Giorgio
Albano, Gianluigi
Lo Presti, Marco
Milella, Antonella
Omenetto, Fiorenzo G.
Farinola, Gianluca M.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2020, 2020 (45) : 6992 - 6996
[3] A highly active catalytic system for Suzuki-Miyaura cross-coupling reactions of aryl and heteroaryl chlorides in water
Mao, Shu-Lan
Sun, Yue
Yu, Guang-Ao
Zhao, Cui
Han, Zhi-Jun
Yuan, Jia
Zhu, Xiaolei
Yang, Qihua
Liu, Sheng-Hua
ORGANIC & BIOMOLECULAR CHEMISTRY, 2012, 10 (47) : 9410 - 9417
[4] Homogeneous and Recyclable Palladium Catalysts: Application in Suzuki-Miyaura Cross-Coupling Reactions
King, Andrew K.
Brar, Aneelman
Li, Guigen
Findlater, Michael
ORGANOMETALLICS, 2023, 42 (17) : 2353 - 2358
[5] Suzuki-Miyaura cross-coupling reactions mediated by palladium/imidazolium salt systems
Grasa, GA
Viciu, MS
Huang, JK
Zhang, CM
Trudell, ML
Nolan, SP
ORGANOMETALLICS, 2002, 21 (14) : 2866 - 2873
[6] Arylcalixarenyl Phosphines in Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions
Elaieb, Fethi
Hedhli, Ahmed
Semeril, David
Matt, Dominique
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, 2016 (10) : 1867 - 1873
[7] New palladium-containing polymers for Suzuki-Miyaura cross-coupling reactions
Crawford, Katherine A.
Cowley, Alan H.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
[8] The Use of Palladium on Magnetic Support as Catalyst for Suzuki-Miyaura Cross-Coupling Reactions
Sydnes, Magne O.
CATALYSTS, 2017, 7 (01):
[9] Reactivity-Tunable Palladium Precatalysts with Favorable Catalytic Properties in Suzuki-Miyaura Cross-Coupling Reactions
Liang, Siou-Wei
Guo, Yingjie
Lee, Wan-Ching
Zeng, Pin-Rui
Lin, Tzu-Hao
Xie, Pei-Zhen
Kang, Hsuan-Hao
Lu, I-Chung
Chang, Yu-Chang
CHEMCATCHEM, 2022, 14 (16)
[10] Suzuki-miyaura cross-coupling reactions of potassium alkenyltrifluoroborates
Molander, GA
Bernardi, CR
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (24): : 8424 - 8429

← 1 2 3 4 5 →