Using Aryl Diazonium Salts in Palladium-Catalyzed Reactions under Safer Conditions

被引：110
作者：
Oger, Nicolas [1 ,2 ]
d'Halluin, Martin [1 ,2 ]
Le Grognec, Erwan [1 ,2 ]
Felpin, Francois-Xavier [1 ,2 ,3 ]
机构：
[1] Univ Nantes, F-44322 Nantes 3, France
[2] CNRS, CEISAM, UFR Sci & Tech, UMR 6230, F-44322 Nantes 3, France
[3] Inst Univ France, F-75005 Paris 5, France
来源：
ORGANIC PROCESS RESEARCH & DEVELOPMENT | 2014年 / 18卷 / 12期
关键词：
HECK-MATSUDA REACTION; ARENEDIAZONIUM TETRAFLUOROBORATE SALTS; REDUCTION-CYCLIZATION HRC; CROSS-COUPLING REACTIONS; CONTINUOUS-FLOW SYNTHESIS; ARYLDIAZONIUM TETRAFLUOROBORATE; O-BENZENEDISULFONIMIDES; SANDMEYER REACTIONS; MEERWEIN ARYLATION; ALKYL NITRITE;
D O I：
10.1021/op500299t
中图分类号：
O69 [应用化学];
学科分类号：
081704 ;
摘要：
In this review, we give a concise but complete overview of methods describing the use of aryl diazonium salts in palladium-catalyzed reactions under safe conditions from a laboratory scale to a multikilogram scale. The approaches summarized herein are critically discussed, highlighting strengths and weaknesses.
引用
收藏
页码：1786 / 1801
页数：16
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