Synthesis of N-Arylquinone Diimine Derivatives of 2H-Benzimidazo[2,1-e]acridine and Their Reactions with Aromatic Amines
- 作者: Slabko O.Y.1, Kaminskii V.A.1
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隶属关系:
- Far Eastern Federal University
- 期: 卷 55, 编号 2 (2019)
- 页面: 152-160
- 栏目: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/219804
- DOI: https://doi.org/10.1134/S1070428019020052
- ID: 219804
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详细
Oxidative coupling of 6,7,8,9,9a,10,11,12,13,14-decahydro-5H-benzimidazo[2,1-e]acridine with reagents containing a primary aromatic amino group forms p-quinone diimines of the 2H-benzimidazo[2,1-e]-acridine series. The subsequent acid-activated 1,4-nucleophilic addition reaction of the products with the same reagents followed by autooxidation gives rise to 3-arylamino-substituted quinone diimines of the specified series.
作者简介
O. Slabko
Far Eastern Federal University
编辑信件的主要联系方式.
Email: slabko.oyu@dvfu.ru
俄罗斯联邦, Universitetskii pr., o. Russkii, Vladivostok, 690902
V. Kaminskii
Far Eastern Federal University
Email: slabko.oyu@dvfu.ru
俄罗斯联邦, Universitetskii pr., o. Russkii, Vladivostok, 690902
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