H-1 and C-13 chemical shifts for tetracycle-fused acridine analogues of amsacrine

Authors
Robin, M Galy, JP Faure, R
Citation
M. Robin et al., H-1 and C-13 chemical shifts for tetracycle-fused acridine analogues of amsacrine, MAGN RES CH, 39(4), 2001, pp. 225-228
Citations number
20
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
MAGNETIC RESONANCE IN CHEMISTRY
ISSN journal
07491581 → ACNP
Volume
39
Issue
4
Year of publication
2001
Pages
225 - 228
Database
ISI
SICI code
0749-1581(200104)39:4<225:HACCSF>2.0.ZU;2-J
Abstract
The H-1 and C-13 NMR resonances for 18 tetracyclic acridines 9-substituted on the acridine ring with Cl, NH2 and AMS [N-(4-amino-3-methoxyphenyl)1meth ane-sulfonamide] groups were completely and unequivocally assigned by the c oncerted application of gs-HMQC and gs-HMBC experiments. For NH2 and AMS su bstituents, the potential amino-imino tautomerism is completely shifted tow ards the imino tautomer. Copyright (C) 2001 John Wiley & Sons, Ltd.