Gold-Catalyzed Synthesis of Iodofulvenes

被引:76
作者
Noesel, Pascal [1 ]
Lauterbach, Tobias [1 ]
Rudolph, Matthias [1 ]
Rominger, Frank [1 ]
Hashmi, A. Stephen K. [1 ]
机构
[1] Heidelberg Univ, Inst Organ Chem, D-69120 Heidelberg, Germany
关键词
alkynes; benzofulvenes; dual activation; gold; iodination; vinylidenes; ORGANOGOLD COMPOUNDS; TERMINAL ALKYNES; HETEROCYCLES; CARBOCYCLES; COMPLEXES; IODINE;
D O I
10.1002/chem.201300507
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the gold-catalyzed synthesis of highly functionalized iodofulvenes from iododialkynes under mild conditions. The catalytic cycle involves the formation of gold acetylides and vinylgold intermediates. These intermediates can then undergo an unprecedented iodine/gold exchange. This new pathway for catalyst transfer in dual gold catalysis opens up the possibility of highly regioselective transformations directed by the gold in the organogold intermediates. The resulting products are well suited for further metal-mediated coupling reactions, allowing the synthesis of extended -systems.
引用
收藏
页码:8634 / 8641
页数:8
相关论文
共 53 条
[1]  
[Anonymous], 2010, ANGEW CHEM INT ED, V49, P5232
[2]  
[Anonymous], 2013, ANGEW CHEM, V125, P2653
[3]  
[Anonymous], 2013, ANGEW CHEM INT ED, V52, P2593
[4]  
[Anonymous], 2011, ANGEW CHEM INT ED, V50, P7226
[5]  
[Anonymous], 2008, ANGEW CHEM INT ED, V47, P7927
[6]  
[Anonymous], 2011, ANGEW CHEM INT ED, V50, P8358
[7]  
[Anonymous], 2012, ANGEW CHEM
[8]  
[Anonymous], 2007, ANGEW CHEM INT ED, V46, P3410
[9]  
[Anonymous], 2012, ANGEW CHEM INT ED, V51, P10633
[10]  
[Anonymous], 2000, ANGEW CHEM INT ED, V39, P4237