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

页码：1111 / 1118

页数：8

共 20 条

[1] Novel reaction between 3,4,5,6-tetrachloro-1,2-benzoquinone and bis-azomethines [J].