Gas-phase cyclisation reactions of 1-(2-arylaminophenyl)alkaniminyl radicals

被引:25
作者
Leardini, R
McNab, H
Nanni, D
Parsons, S
Reed, D
Tenan, AG
机构
[1] Univ Edinburgh, Dept Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
[2] Univ Bologna, Dipartimento Chim Organ A Mangini, I-40136 Bologna, Italy
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1998年 / 11期
关键词
D O I
10.1039/a800886h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Flash vacuum pyrolysis (FVP) of the oxime ethers 9-11 at 650 degrees C (10(-2)-10(-3) Torr) gives products such as the nitrile 17, carbazoles 19 and 20 and acridines 18 and 21 derived from the corresponding iminyl radicals 13-15. The mechanism proposed for the formation of the acridines involves a key hydrogen abstraction by the iminyl of the adjacent N-H atom. When this route is blocked by an N-methyl group, as in 12, alternative cyclisations ensue, yielding the dihydroquinazoline 26 (via another hydrogen abstraction process) and the benzimidazole 25 (via an iminyl-imidoyl interconversion).
引用
收藏
页码:1833 / 1838
页数:6
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