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
收藏
页码：545 / 548
页数：4
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