REACTION OF TETRAOXOPYRROLO[2,3-D]PYRIMIDINES, ISATIN ANALOGS, WITH ORTHO-PHENYLENEDIAMINE

被引：9

作者：

BERNIER, JL

HENICHART, JP

机构：

[1] Unité Inserm U16, Lille, 59045, Place de Verdun

来源：

JOURNAL OF HETEROCYCLIC CHEMISTRY | 1979年 / 16卷 / 04期

关键词：

D O I：

10.1002/jhet.5570160421

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

In the course of general studies on new antitumor tetracyclic intercalating agents, the condensation of o‐phenylenediamine with two new tetraoxopyrrolo[2,3‐d]pyrimidine derivatives has been carried out. The structure of the reaction products as arylketimines has been elucidated and mass spectral fragmentations are discussed. Copyright © 1979 Journal of Heterocyclic Chemistry

引用

页码：717 / 720

页数：4

共 25 条

[1] REARRANGEMENT AND CYCLIZATION REACTIONS IN MASS SPECTRA OF A SERIES OF ISATIN CARBONYL DERIVATIVES OF MEDICINAL INTEREST - 2-OXO-3-INDOLINYLIDENE ANILS (N-ARYLKETIMINES), 2-OXO-3-INDOLINYLIDENE PHENYLHYDRAZONES, 2-OXO-3,3-BIS-(O-DIAMINOARYL) INDOLYL DERIVATIVES AND THEIR 2,3-QUINOXALINE HETEROCYCLIC ANALOGUES [J].