Reaction of diimines and benzyne

被引：63
|
作者：
Aly, AA [1 ]
Mohamed, NK [1 ]
Hassan, AA [1 ]
Mourad, AFE [1 ]
机构：
[1] El Minia Univ, Fac Sci, Dept Chem, El Minia, Egypt
来源：
TETRAHEDRON | 1999年 / 55卷 / 04期
关键词：
D O I：
10.1016/S0040-4020(98)01089-8
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The reaction between benzyne and the Schiff bases 1a,b and 15a,b leads to the 1,4-bis(2'-substituted acridin-10-yl)benzene 4a,b, the N-phenylarylamines 10a,b and the 10-(4'-formylphenyl)-substituted acridines iia,b (from la,b) and the a-substituted acridine-10-carboxyaldehyde 18a,b (from 15a,b). Cyclohexyl (4-cyclohexyliminomethylbenzylidine)amine 1c reacts with benzyne by an ene-reaction to give cyclohexenyl[(4-cyclchexyliminomethylphenyl)benzylidine]amine 14. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码：1111 / 1118
页数：8
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