Complete and unambiguous assignments of 1H and 13C chemical shifts of new arylamino derivatives of ortho-naphthofuranquinones |
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Authors: | da Silva Júnior Eufrânio N de Souza Maria Cecília B V Pinto Antônio V Pinto Maria do Carmo F R Nogueira Christiane M Ferreira Vitor F Azeredo Rodrigo B V |
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Institution: | Universidade Federal Fluminense, Instituto de Química, Departamento de Química Organica, Campus do Valonguinho, 24020-141, Niterói, RJ, Brazil. |
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Abstract: | Six new nor-beta-lapachones have been synthesized from reaction of 3-bromo-nor-beta-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). |
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Keywords: | NMR 1H NMR 13C NMR naphthofuranquinones nor‐β‐lapachones |
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