1H and 13C chemical shifts for acridines:: XVII.: (1,3-Benzothiazol-2-yl)amino-9(10H)-acridinone derivatives

被引：10

作者：

Avellaneda, A

Robin, M

Faure, R

Périchaud, A

Galy, JP

机构：

[1] Univ Aix Marseille 3, Lab Valorisat Chim Fine, Case 552, Fac Sci & Tech St Jerome, F-13397 Marseille 20, France

[2] Lab Chim Macromol, F-13331 Marseille, France

来源：

MAGNETIC RESONANCE IN CHEMISTRY | 2002年 / 40卷 / 08期

关键词：

NMR; H-1; C-13; 2D NMR; acridin-9(10H)-ones; 2-amino-1,3-benzothiazoles; hydrogen bond; amino-imino tautomerism;

D O I：

10.1002/mrc.1049

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The H-1 and C-13 NMR resonances for 16 acridin-9(10H)-ones substituted with amino or (1,3-benzothiazol-2-yl)amino groups were completely and unequivocally assigned by the concerted application of gs-COSY, gs-HMQC and gs-HMBC experiments. Evidence for hydrogen bond and amino-imino tautomerism is presented for 1- and 4-substituted acridin-9(10H)-ones. Copyright (C) 2002 John Wiley Sons, Ltd.

引用

页码：545 / 548

页数：4

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