Beyond the traditional roles of Ag in catalysis: the transmetalating ability of organosilver(i) species in Pd-catalysed reactions

被引:51
作者
Mudarra, Angel L. [1 ,2 ]
Martinez de Salinas, Sara [1 ]
Perez-Temprano, Monica H. [1 ]
机构
[1] Inst Chem Res Catalonia ICIQ, Avgda Paisos Catalans 16, Tarragona 43007, Spain
[2] Univ Rovira & Virgili, Dept Quim Analit & Quim Organ, C Marcel li Domingo S-N, Tarragona 43007, Spain
关键词
C-H ACTIVATION; REDUCTIVE ELIMINATION; BIMETALLIC CATALYSIS; CARBOXYLIC-ACIDS; DIRECT ARYLATION; COUPLING REACTION; SILVER COMPOUNDS; COMPLEXES; TRIFLUOROMETHYLATION; DIFLUOROMETHYLATION;
D O I
10.1039/c8ob02611d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Silver salts are one of the most widely used additives in Pd-catalysed transformations. Apart from acting as a halide scavenger and/or an external oxidant, over the past decade it has been revealed that silver salts can play other roles such as a C-H activation promoter or decarboxylating agent, generating organosilver (I) species. These nucleophiles can promote innovative transformations by reacting with PdII intermediates through a transmetalation step. This review article covers different Pd-catalysed C-C bond-forming reactions where silver complexes have been proposed to act as nucleophilic coupling partners. We will also provide relevant mechanistic features associated with these transformations.
引用
收藏
页码:1655 / 1667
页数:13
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