Fundamental Basis for Implementing Oxidant-Free Au(I)/Au(III) Catalysis

被引:71
作者
Font, Pau [1 ,2 ]
Ribas, Xavi [1 ,2 ]
机构
[1] Univ Girona, Inst Quim Computac & Catalisi IQCC, QBIS CAT Grp, Campus Montilivi, Girona 17003, Catalonia, Spain
[2] Univ Girona, Dept Quim, Campus Montilivi, Girona 17003, Catalonia, Spain
关键词
Gold; Au(I); Au(III); Cross coupling; Oxidant-free; Catalysis; CROSS-COUPLING REACTIONS; C-H ACTIVATION; GOLD(I)-CATALYZED INTRAMOLECULAR HYDROAMINATION; OXIDATIVE ADDITION-REACTIONS; CATIONIC GOLD(I) COMPLEXES; VISIBLE-LIGHT PHOTOREDOX; REDUCTIVE ELIMINATION; ORGANIC-SYNTHESIS; TERMINAL ALKYNES; DUAL GOLD;
D O I
10.1002/ejic.202100301
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Oxidant-free Au(I)/Au(III) catalysis can still be regarded as a young and promising chemistry. Because the first examples of gold catalysis were limited to the activation and functionalization of pi-C-C bonds and very little was known on fundamental organometallic transformations at gold, countless works during the past 15 years have been devoted to disclosing the elementary reactivity of gold and implementing it in catalysis. Remarkably, great emphasis on triggering oxidative addition at Au(I) has been placed, as the high redox potential of the Au(I)/Au(III) pair disfavors this reaction. In fact, different strategies such as strain release, ligand design and photochemistry have been proven successful at allowing the bottleneck oxidative addition to occur. These approaches have led to the rational development of oxidant-free Au(I)/Au(III) redox catalysis, particularly catalytic cycles in cross-coupling transformations where oxidative addition is usually the entry point to the cycle. Herein, the background story, the development process, and relevant examples of oxidant-free gold-catalyzed cross-coupling reactions are reviewed.
引用
收藏
页码:2556 / 2569
页数:14
相关论文
共 188 条
[1]   Reductive C(sp2)-N Elimination from Isolated Pd(IV) Amido Aryl Complexes Prepared Using H2O2 as Oxidant [J].
Abada, Elikplim ;
Zavalij, Peter Y. ;
Vedernikov, Andrei N. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (02) :643-646
[2]   Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines [J].
Akram, Manjur O. ;
Das, Avishek ;
Chakrabarty, Indradweep ;
Patil, Nitin T. .
ORGANIC LETTERS, 2019, 21 (19) :8101-8105
[3]   Oxidant-free oxidative gold catalysis: the new paradigm in cross-coupling reactions [J].
Akram, Manjur O. ;
Banerjee, Somsuvra ;
Saswade, Sagar S. ;
Bedi, Vaibhav ;
Patil, Nitin T. .
CHEMICAL COMMUNICATIONS, 2018, 54 (79) :11069-11083
[4]   Gold(I)-catalyzed cross-coupling reactions of aryldiazonium salts with organostannanes [J].
Akram, Manjur O. ;
Shinde, Popat S. ;
Chintawar, Chetan C. ;
Patil, Nitin T. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2018, 16 (16) :2865-2869
[5]   Domino Meyer-Schuster/Arylation Reaction of Alkynols or Alkynyl Hydroperoxides with Diazonium Salts Promoted by Visible Light under Dual Gold and Ruthenium Catalysis [J].
Alcaide, Benito ;
Almendros, Pedro ;
Busto, Eduardo ;
Luna, Amparo .
ADVANCED SYNTHESIS & CATALYSIS, 2016, 358 (09) :1526-1533
[6]  
[Anonymous], 2006, ANGEW CHEM-GER EDIT
[7]  
[Anonymous], 2011, ANGEW CHEM
[8]  
[Anonymous], 2013, ANGEW CHEM
[9]   REACTIVITY OF CARBON-METAL BONDS IN ORGANOGOLD(I) COMPLEXES CONTAINING ORTHO-VINYLPHENYL AND ORTHO-ALLYLPHENYL LIGANDS [J].
ARESTA, M ;
VASAPOLLO, G .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1973, 50 (01) :C51-C53
[10]   Reversible Oxidative Addition and Reductive Elimination of Fluorinated Disulfides at Gold(I) Thiolate Complexes: A New Ligand Exchange Mechanism [J].
Bachman, Robert E. ;
Bodolosky-Bettis, Sheri A. ;
Pyle, Chelsea J. ;
Gray, Margaret Anne .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (43) :14303-14310