Transition metal-catalyzed N-arylations of amidines and guanidines

被引:175
|
作者
Rauws, Tom R. M. [1 ]
Maes, Bert U. W. [1 ]
机构
[1] Univ Antwerp, Dept Chem, B-2020 Antwerp, Belgium
关键词
CROSS-COUPLING REACTIONS; C-N; ARYL HALIDES; HIGHLY EFFICIENT; COORDINATION CHEMISTRY; AMINATION REACTION; CASCADE REACTIONS; O-HALOANILINES; AZA ANALOGS; COPPER;
D O I
10.1039/c1cs15236j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although several recent reviews dealt with transition metal catalyzed N-arylation of amines (all classes), to date no specific review covering the N-arylation of amidines and guanidines appeared. Amidines and guanidines are considered as fundamental entities in medicinal chemistry. The appearance of these functional groups in drugs, agrochemicals and natural products justifies a separate description of the current status of the literature on the N-arylation of the amidine and guanidine functionalities. Both acyclic and cyclic derivatives are taken into account. For cyclic amidines/guanidines only systems which possess an exocyclic nitrogen atom are considered. This critical review is largely organized by the type of amidine/guanidine and transition metal used and covers literature up to May 2011 (200 references).
引用
收藏
页码:2463 / 2497
页数:35
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