817160-11-5Relevant articles and documents
1H and 13C NMR spectral data of p-nitrobenzenesulfonamides and dansylsulfonamides derived from N-alkylated o-(Purinemethyl)anilines
Morales, Fátima,Campos, Joaquín M.,Conejo-García, Ana
, p. 760 - 770 (2017/07/13)
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Synthesis of tetrahydrobenzoxazepine acetals with electron-withdrawing groups on the nitrogen atom. Novel scaffolds endowed with anticancer activity against breast cancer cells
Díaz-Gavilán, Mónica,Rodríguez-Serrano, Fernando,Gómez-Vidal, José A.,Marchal, Juan A.,Aránega, Antonia,Gallo, Miguel á.,Espinosa, Antonio,Campos, Joaquín M.
, p. 11547 - 11557 (2007/10/03)
Synthetic approaches that have led to (RS)-3-methoxy-N-substituded-1,2,3,5- tetrahydro-4,1-benzoxazepines with different electron-withdrawing groups, and (RS)-2-methoxy-N-trifluoroacetyl-2,3,4,5-tetrahydro-1,4-benzoxazepine are described. These novel synthons that were designed to be used as scaffolds for the preparation of new O,N-acetals as anticancer agents, unexpectedly proved to show antiproliferative activity against the MCF-7 breast cancer cell line. It has been found that substituents on the nitrogen atom have an influence on biological activity. In particular, the presence of a trifluoroacetyl moiety on the nitrogen atom leads to amides displaying interesting in vitro antitumour activities. Graphical Abstract.