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

✍ Scribed by A. Avellaneda; M. Robin; R. Faure; A. Périchaud; J.-P. Galy

Publisher: John Wiley and Sons
Year: 2002
Tongue: English
Weight: 94 KB
Volume: 40
Category: Article
ISSN: 0749-1581
DOI: 10.1002/mrc.1049

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✦ Synopsis

Abstract

The ^1^H and ^13^C NMR resonances for 16 acridin‐9(10__H__)‐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(10__H__)‐ones. Copyright © 2002 John Wiley & Sons, Ltd.

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