Abstract
Symmetrical and unsymmetrical 3-halo- or 3-methoxy- substituted 2-dibenzoylamino- 1,4-naphthoquinone analogs were synthesized with an average yield of 45% via sodium hydride promoted bis-acylation of 2-amino-3-chloro-1,4- naphthoquinone, 2-amino-3-bromo- 1,4-naphthoquinone and 2-amino-3-methoxy-1,4- naphthoquinone. © 2013 by the authors.
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Brandy, Y., Brandy, N., Akinboye, E., Lewis, M., Mouamba, C., MacK, S., … Bakare, O. (2013). Synthesis and characterization of novel unsymmetrical and symmetrical 3-halo- or 3-methoxy-substituted 2-dibenzoylamino-1,4-naphthoquinone derivatives. Molecules, 18(2), 1973–1984. https://doi.org/10.3390/molecules18021973
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