## Abstract The complete analyses of the ^1^H and ^13^C NMR spectra of the __ortho__ ester analogues of etoposide are reported and differentiation of the α and β isomers of these derivatives is suggested by using the γ‐__gauche__ effect upon the ^13^C chemical shift. Copyright © 2003 John Wiley & S
Complete and unambiguous assignments of 1H and 13C chemical shifts of new arylamino derivatives of ortho-naphthofuranquinones
✍ Scribed by Eufrânio N. da Silva Júnior; Maria Cecília B. V. de Souza; Antônio V. Pinto; Maria do Carmo F. R. Pinto; Christiane M. Nogueira; Vitor F. Ferreira; Rodrigo B. V. Azeredo
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 211 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2250
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✦ Synopsis
Abstract
Six new nor‐β‐lapachones have been synthesized from reaction of 3‐bromo‐nor‐β‐lapachone with arylamines. These derivatives have potent anticancer properties against several cell lines. Here, we report complete unambiguous assignments of ^1^H and ^13^C chemical shifts of the new compounds. The assignments were made using a combination of one‐ and two‐dimensional NMR techniques (^1^H, ^13^C, ^1^H^1^H COSY, ^1^H^13^C HSQC, and ^1^H^13^C HMBC). Copyright © 2008 John Wiley & Sons, Ltd.
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