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

✍ Scribed by M. Robin; J. P. Galy; R. Faure

Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
98 KB
Volume
39
Category
Article
ISSN
0749-1581

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✦ Synopsis

Abstract

The ^1^H and ^13^C NMR resonances for 18 tetracyclic acridines 9‐substituted on the acridine ring with Cl, NH~2~ and AMS [N‐(4‐amino‐3‐methoxyphenyl)1methanesulfonamide] groups were completely and unequivocally assigned by the concerted application of gs‐HMQC and gs‐HMBC experiments. For NH~2~ and AMS substituents, the potential amino–imino tautomerism is completely shifted towards the imino tautomer. Copyright © 2001 John Wiley & Sons, Ltd.

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