Gold(I)-Catalyzed Cross-Coupling Reactions of Arenediazonium Salts with Alkynoic Acids

被引：4

作者：

Abrams, J. N. ^{[1
]}

Chi, B. K. ^{[1
]}

机构：

[1] Texas A&M Univ, Dept Chem, Kingsville, TX 78363 USA

来源：

RUSSIAN JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 56卷 / 07期

关键词：

Sonogashira; decarboxylative; diazonium salt; alkanoic acid; gold(I); HALIDE DEAMINATION REACTIONS; CARBOXYLIC-ACIDS; TETRAFLUOROBORATE SALTS; ARYLDIAZONIUM SALTS; DIAZONIUM SALTS; PALLADIUM; GOLD; CATALYSIS; NITRITE; NPS;

D O I：

10.1134/S1070428020070180

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of simple alkynoate salts with isolated arenediazonium tetrafluoroborate salts that had been pre-conditioned with the gold(I) catalyst AuCl(Me2S) led to the formation of cross-coupled products via a decarboxylative Sonogashira reaction process in modest yield and under mild conditions. The major by-product is a defunctionalized aryl moiety stemming from the diazonium salt, which competitively forms via hydrodediazonation. Good functional group tolerance and reaction site selectivity were attained in this limited investigation.

引用

页码：1236 / 1244

页数：9

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