An Alternative to the Classical α-Arylation: The Transfer of an Intact 2-Iodoaryl from ArI(O2CCF3)2

被引:93
|
作者
Jia, Zhiyu [1 ,2 ]
Galvez, Erik [1 ,2 ]
Maria Sebastian, Rosa [1 ,2 ]
Pleixats, Roser [1 ,2 ]
Alvarez-Larena, Angel [3 ]
Martin, Eddy [4 ]
Vallribera, Adelina [1 ,2 ]
Shafir, Alexandr [4 ]
机构
[1] Univ Autonoma Barcelona, Dept Chem, Bellaterra, Spain
[2] Univ Autonoma Barcelona, Ctr Innovac Quim Avanzada ORFEO CINQA, Bellaterra, Spain
[3] Univ Autonoma Barcelona, Serv Difraccio Raigs 10, Bellaterra, Spain
[4] Inst Chem Res Catalonia ICIQ, Tarragona 43007, Spain
关键词
alpha-arylation; C-H functionalization; iodonium-Claisen rearrangement; dehydrogenative C-C coupling; hypervalent iodine; DIARYLIODONIUM SALTS; ARYL HALIDES; PHENYLATION; REARRANGEMENT; GENERATION; KETONES; YLIDES; ESTERS; COPPER;
D O I
10.1002/anie.201405982
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The -arylation of carbonyl compounds is generally accomplished under basic conditions, both under metal catalysis and via aryl transfer from the diaryl (3)-iodanes. Here, we describe an alternative metal-free -arylation using ArI(O2CCF3)(2) as the source of a 2-iodoaryl group. The reaction is applicable to activated ketones, such as -cyanoketones, and works with substituted aryliodanes. This formal CH functionalization reaction is thought to proceed through a [3,3] rearrangement of an iodonium enolate. The final -(2-iodoaryl)ketones are versatile synthetic building blocks.
引用
收藏
页码:11298 / 11301
页数:4
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