Oxidative SNH amidation of acridine and tautomerism of N-(acridin-9-yl)benzamides

被引：7

作者：

Demidov, Oleg P. ^{[1
]}

Borovlev, Ivan V. ^{[1
]}

Amangasieva, Gulminat A. ^{[1
]}

Avakyan, Elena K. ^{[1
]}

机构：

[1] North Caucasus Fed Univ, 1a Pushkina St, Stavropol 355009, Russia

来源：

CHEMISTRY OF HETEROCYCLIC COMPOUNDS | 2016年 / 52卷 / 02期

关键词：

PALLADIUM-CATALYZED AMINATION; NUCLEOPHILIC AROMATIC-SUBSTITUTION; PROTOTROPIC TAUTOMERISM; ANTITUMOR AGENTS; AQUEOUS-MEDIUM; ARYL AZIDES; 1,3,7-TRIAZAPYRENES; ALKYLAMINATION; HYDROGEN; ALKOXYLATION;

D O I：

10.1007/s10593-016-1841-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Direct oxidative nucleophilic substitution of hydrogen atom in acridine molecule was used to synthesize 9-acylaminoacridines. The prototropic amine-imine tautomerism of these compounds was studied.

引用

页码：104 / 109

页数：6

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