First palladium-catalyzed aminations of aryl chlorides

被引:99
|
作者
Beller, M
Riermeier, TH
Reisinger, CP
Herrmann, WA
机构
[1] Anorganisch-chemisches Institut, TU München
关键词
D O I
10.1016/S0040-4039(97)00289-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The palladium-catalyzed coupling reaction of aryl chlorides with various amines has been studied for the first rime. Crucial for the success of this C-N bond forming reaction is the use of potassium tertbutoxide as base. Turn over numbers up to 900 and yields up to 80 % have been obtained. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:2073 / 2074
页数:2
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