RETRACTED: The amine-catalysed Suzuki-Miyaura-type coupling of aryl halides and arylboronic acids (Retracted Article)

被引：17

作者：

Xu, Lei ^{[1
]}

Liu, Fu-Yue ^{[1
]}

Zhang, Qi ^{[1
]}

Chang, Wei-Jun ^{[1
]}

Liu, Zhong-Lin ^{[1
]}

Lv, Ying ^{[2
]}

Yu, Hai-Zhu ^{[2
]}

Xu, Jun ^{[1
]}

Dai, Jian-Jun ^{[1
]}

Xu, Hua-Jian ^{[1
]}

机构：

[1] Hefei Univ Technol, Anhui Prov Key Lab Adv Catalyt Mat & React Engn, Inst Ind & Equipment Technol, Sch Food & Biol Engn,Sch Chem & Chem Engn, Hefei, Peoples R China

[2] Anhui Univ, Dept Chem, Anhui Prov Key Lab Chem Inorgan Organ Hybrid Func, Hefei, Peoples R China

来源：

NATURE CATALYSIS | 2021年 / 4卷 / 01期

基金：

中国国家自然科学基金;

关键词：

PINCER COMPLEXES; METAL; PALLADIUM; DERIVATIVES; MECHANISMS; EFFICIENT; RECEPTOR; BIARYLS; ALKYNES;

D O I：

10.1038/s41929-020-00564-z

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

Suzuki-Miyaura coupling is a practical and attractive carbon-carbon bond formation reaction due to its high efficiency and wide functional group compatibility, but its industrial applications are limited because it is typically catalysed by expensive palladium-containing transition-metal complexes. Here we show a robust and chemoselective organocatalytic Suzuki-Miyaura-type coupling of aryl halides with arylboronic acids catalysed by amines. The utility and scope of this reaction were demonstrated by the synthesis of several commercially relevant small molecules and a selection of derivatives of pharmaceutical drugs.

引用

页码：71 / 78

页数：8

共 50 条

[41] Palladium-Catalyzed Suzuki-Miyaura Type Coupling Reaction of Aryl Halides with Triphenylborane-Pyridine
Yang Minghua
Gu Yongbing
Wang Yan
Zhao Xiyu
Yan Guobing
CHINESE JOURNAL OF CHEMISTRY, 2012, 30 (10) : 2581 - 2586
[42] RETRACTED: Schiff base transition metal complexes for Suzuki-Miyaura cross-coupling reaction (Retracted article. See vol. 134, 2022)
Ansari, Rasheeda M.
Bhat, Badekai Ramachandra
JOURNAL OF CHEMICAL SCIENCES, 2017, 129 (09) : 1483 - 1490
[43] Efficient palladium-catalyzed Suzuki-Miyaura coupling of aryl chlorides with arylboronic acids using benzoferrocenyl phosphines as supporting ligands
Thimmaiah, Muralidhara
Fang, Shiyue
TETRAHEDRON, 2007, 63 (29) : 6879 - 6886
[44] High Surface Area CeO2 Promoted Suzuki-Miyaura Cross-Coupling of Arylboronic Acids and Aryl Iodides
Graziano Mayer, Marilyn
Nador, Fabiana
Alicia Volpe, Maria
Radivoy, Gabriel
SYNLETT, 2013, 24 (03) : 338 - 342
[45] A highly active and recyclable homogeneous NHC-palladium catalyst with pH- and light-sensitive tags for the Suzuki-Miyaura coupling reactions of aryl halides with arylboronic acids
Liu, Guiyan
Liu, Chengxin
Zhao, Xia
Wang, Jianhui
RSC ADVANCES, 2016, 6 (50): : 44475 - 44479
[46] RETRACTED: Iron-Catalyzed Suzuki-Miyaura Cross-Coupling Reaction (Retracted article. See vol. 352, pg. 1081, 2010)
Bezier, David
Darcel, Christophe
ADVANCED SYNTHESIS & CATALYSIS, 2009, 351 (11-12) : 1732 - 1736
[47] Cooperative Photoredox and N-Heterocyclic Carbene Catalysis Suzuki-Miyaura-Type Reaction: Radical Coupling of Aroyl Fluorides and Alkyl Boronic Acids
Li, Shihao
Zhang, Chaoyang
Wang, Sheng
Yang, Wenqing
Fang, Xinru
Fan, Shilu
Zhang, Qi
Li, Xiao-Xuan
Feng, Yi-Si
ORGANIC LETTERS, 2024, 26 (08) : 1728 - 1733
[48] Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids
Roslin, Sara
Odell, Luke R.
CHEMICAL COMMUNICATIONS, 2017, 53 (51) : 6895 - 6898
[49] A simple and highly efficient P,O-type ligand for Suzuki-Miyaura cross-coupling of aryl halides
Kwong, FY
Lam, WH
Yeung, CH
Chan, KS
Chan, ASC
CHEMICAL COMMUNICATIONS, 2004, (17) : 1922 - 1923
[50] A convenient method for preparing aromatic ketones from acyl chlorides and arylboronic acids via Suzuki-Miyaura type coupling reaction
Urawa, Y
Ogura, K
TETRAHEDRON LETTERS, 2003, 44 (02) : 271 - 273

← 1 2 3 4 5 →