Recent advances in Ullmann reaction:: Copper(II) diacetate catalysed N-, O- and S-arylation involving polycoordinate heteroatomic derivatives

被引:125
作者
Finet, JP [1 ]
Fedorov, AY
Combes, S
Boyer, G
机构
[1] Univ Aix Marseille 1, UMR 6517 CNRS, Lab Chim Organ Synthese, Fac Sci St Jerome, F-13397 Marseille 20, France
[2] Univ Aix Marseille 3, UMR 6517 CNRS, Lab Chim Organ Synthese, Fac Sci St Jerome, F-13397 Marseille 20, France
[3] Nizhnii Novgorod Lobachevski State Univ, Dept Organ Chem, Nizhnii Novgorod 603600, Russia
[4] Univ Aix Marseille 3, UMR 6009 CNRS, Lab Valorisat Chim Fine, Fac Sci St Jerome, F-13397 Marseille 20, France
关键词
D O I
10.2174/1385272023374058
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Copper-catalyzed O- and N-arylation reactions involving triarylbismuth diacetates or aryllead triacetates are ligand coupling reactions which were discovered in the eighties independently by Barton's and Dodonov's groups. These reagents lead generally to efficient arylation under mild neutral conditions (room temperature or 40degreesC, no added basic reagent). Recently, the scope of these main group metal mediated reactions was broadened when Chan and Evans reported that organoboron compounds can be used as the source of the organic aryl ligand. Subsequently, organosiloxanes, organostannanes and diaryliodonium salts proved also to be efficient reagents for these mild copper catalyzed O- and N-arylation reactions. Organoantimony compounds were also used but appeared to be less efficient reagents.
引用
收藏
页码:597 / 626
页数:30
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