A General Palladium-Catalyzed Hiyama Cross-Coupling Reaction of Aryl and Heteroaryl Chlorides

被引:36
|
作者
Yuen, On Ying [1 ,2 ,3 ]
So, Chau Ming [1 ,2 ,3 ]
Man, Ho Wing [1 ,2 ]
Kwong, Fuk Yee [1 ,2 ,3 ]
机构
[1] Hong Kong Polytech Univ, State Key Lab Chirosci, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
[3] Hong Kong Polytech Univ, Shenzhen Res Inst SZRI, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
aryl chlorides; aryl(alkoxy)silane; cross-coupling reaction; palladium; phosphine ligand; EFFICIENT LIGAND; ORGANOTIN REAGENTS; VINYL CHLORIDES; ORGANIC HALIDES; BOND FORMATION; BROMIDES; SILOXANE; SUZUKI; ARYLTRIALKOXYSILANES; DERIVATIVES;
D O I
10.1002/chem.201600420
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A general palladium-catalyzed Hiyama cross-coupling reaction of aryl and heteroaryl chlorides with aryl and heteroaryl trialkoxysilanes by a Pd(OAc)(2)/L2 catalytic system is presented. A newly developed water addition protocol can dramatically improve the product yields. The conjugation of the Pd/L2 system and the water addition protocol can efficiently catalyze a broad range of electron-rich, -neutral, -deficient, and sterically hindered aryl chlorides and heteroaryl chlorides with excellent yields within three hours and the catalyst loading can be down to 0.05mol% Pd for the first time. Hiyama coupling of heteroaryl chlorides with heteroaryl silanes is also reported for the first time. The reaction can be easily scaled up 200times (100mmol) without any degasification and purification of reactants; this facilitates the practical application in routine synthesis.
引用
收藏
页码:6471 / 6476
页数:6
相关论文
共 50 条
  • [31] Palladium-catalyzed cross-coupling reaction of tricyclopropylbismuth with aryl halides and triflates
    Gagnon, Alexandre
    Duplessis, Martin
    Alsabeh, Pamela
    Barabe, Francis
    JOURNAL OF ORGANIC CHEMISTRY, 2008, 73 (09): : 3604 - 3607
  • [32] Palladium-Catalyzed Cross-Coupling Reaction of Thioglycosides with (Hetero)aryl Halides
    Brachet, Etienne
    Brion, Jean-Daniel
    Messaoudi, Samir
    Alami, Mouad
    ADVANCED SYNTHESIS & CATALYSIS, 2013, 355 (2-3) : 477 - 490
  • [33] PALLADIUM-CATALYZED CROSS-COUPLING REACTIONS OF POTASSIUM N-METHYLTRIFLUOROBORATE ISOINDOLIN-1-ONE WITH ARYL AND HETEROARYL CHLORIDES
    Nadaf, Rashid N.
    Seapy, Dave G.
    SYNTHETIC COMMUNICATIONS, 2014, 44 (14) : 2012 - 2020
  • [34] Palladium-catalyzed denitrogenative Hiyama cross-coupling with arylhydrazines under air
    Zhang, Hui
    Wang, Chunjie
    Li, Zhiwei
    Wang, Ziyun
    TETRAHEDRON LETTERS, 2015, 56 (40) : 5371 - 5376
  • [35] Palladium-catalyzed cross-coupling of trimethoxysilylbenzene with aryl bromides and chlorides using phosphite ligands
    Ju, Jinhun
    Nam, Hyungoog
    Jung, Hyun Min
    Lee, Sunwoo
    TETRAHEDRON LETTERS, 2006, 47 (49) : 8673 - 8678
  • [36] Palladium-Catalyzed Desulfitative Cross-Coupling Reaction of Sodium Sulfinates with Benzyl Chlorides
    Zhao, Feng
    Tan, Qi
    Xiao, Fuhong
    Zhang, Shufeng
    Deng, Guo-Jun
    ORGANIC LETTERS, 2013, 15 (07) : 1520 - 1523
  • [37] Ligand-supported palladium-catalyzed cross-coupling reactions of (hetero) aryl chlorides
    Onoabedje, Efeturi Abraham
    Okoro, Uchechukwu Chris
    SYNTHETIC COMMUNICATIONS, 2019, 49 (17) : 2117 - 2146
  • [38] Palladium-Catalyzed Cross-Coupling of Aryl Bromides and Chlorides with Trimethylsilylalkynes under Mild Conditions
    Tlahuext-Aca, Adrian
    Nguyen, Quyen D.
    Gao, Yang
    Sati, Girish C.
    Zhao, Jinpeng
    Valco, Daniel
    JOURNAL OF ORGANIC CHEMISTRY, 2024, 89 (18): : 13762 - 13767
  • [39] The palladium-catalyzed cross-coupling reactions of trifluoroethyl iodide with aryl and heteroaryl boronic acid esters
    Liang, Apeng
    Li, Xinjian
    Liu, Dongfeng
    Li, Jingya
    Zou, Dapeng
    Wu, Yangjie
    Wu, Yusheng
    CHEMICAL COMMUNICATIONS, 2012, 48 (66) : 8273 - 8275
  • [40] D-Glucosamine as a Green Ligand for Palladium-Catalyzed Cross-Coupling of Aryl and Heteroaryl Halides
    Jha, Abadh Kishor
    Shahni, Rahul Kumar
    Jain, Nidhi
    SYNLETT, 2015, 26 (02) : 259 - 264