Gold Catalysis and Fluorine

被引:29
作者
Hopkinson, Matthew N. [1 ]
Gee, Antony D. [2 ]
Gouverneur, Veronique [1 ]
机构
[1] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England
[2] Kings Coll London, St Thomas Hosp, Div Imaging Sci & Bioengn, London SE1 7EH, England
基金
英国工程与自然科学研究理事会;
关键词
C-C coupling; cross-coupling; fluorine; gold; homogeneous catalysis; OXIDATIVE COUPLING REACTIONS; C-C; GOLD(I)-CATALYZED FORMATION; DIRECT ALKYNYLATION; ADDITION-REACTIONS; HYDROGEN-FLUORIDE; SYNTHETIC METHODS; BOND FORMATION; REACTIVITY; CYCLIZATION;
D O I
10.1002/ijch.201000078
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Performing gold-catalyzed organic transformations in the presence of fluorinating reagents can lead to both fluorinated and non-fluorinated products. Gold(I) complexes can activate alkynes towards nucleophilic attack by fluoride leading to fluoroalkenes under mild conditions. Fluorinated products can also be prepared upon performing gold-catalyzed transformations in the presence of electrophilic sources of fluorine. In most cases, however, the combination of gold and electrophilic fluorinating reagents does not lead to fluorination but delivers products of oxidative homo- or cross-coupling. In these processes the "F+" source is likely acting as a sacrificial two-electron external oxidant performing the key oxidation of gold(I) to gold(III) in the redox cycle. Oxidative coupling is an emerging field of gold catalysis which, when combined with the well-established reactivity of gold as a soft pi.-acid, holds promise as a mild and efficient method for the construction of complex organic molecules.
引用
收藏
页码:675 / 690
页数:16
相关论文
共 121 条
[1]   Reversible C-F bond formation and the Au-catalyzed hydrofluorination of alkynes [J].
Akana, Jennifer A. ;
Bhattacharyya, Koyel X. ;
Mueller, Peter ;
Sadighi, Joseph P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (25) :7736-+
[2]   TETRABUTYLAMMONIUM AND POLYMER-SUPPORTED DIHYDROGENTRIFLUORIDE - NEW HYDROFLUORINATING REAGENTS FOR ELECTROPHILIC ALKYNES [J].
ALBERT, P ;
COUSSEAU, J .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (14) :961-962
[3]  
[Anonymous], 2010, ANGEW CHEM
[4]  
[Anonymous], 2007, ANGEW CHEM-GER EDIT
[5]   Alternative synthetic methods through new developments in catalysis by gold [J].
Arcadi, Antonio .
CHEMICAL REVIEWS, 2008, 108 (08) :3266-3325
[6]   3,3′-Bis(arylbenzofurans) via a Gold-Catalyzed Domino Process [J].
Auzias, Mathieu G. ;
Neuburger, Markus ;
Wegner, Hermann A. .
SYNLETT, 2010, (16) :2443-2448
[7]   Arylsilanes: Application to Gold-Catalyzed Oxyarylation of Alkenes [J].
Ball, Liam T. ;
Green, Michael ;
Lloyd-Jones, Guy C. ;
Russell, Christopher A. .
ORGANIC LETTERS, 2010, 12 (21) :4724-4727
[8]   Synthesis and Reactivity of a Mono-σ-Aryl Palladium(IV) Fluoride Complex [J].
Ball, Nicholas D. ;
Sanford, Melanie S. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (11) :3796-+
[9]  
Brand J. P., 2009, ANGEW CHEM, V121, P9510
[10]   Direct Alkynylation of Thiophenes: Cooperative Activation of TIPS-EBX with Gold and Bronsted Acids [J].
Brand, Jonathan P. ;
Waser, Jerome .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (40) :7304-7307