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da Silva Júnior EN de Souza MC Pinto AV Pinto Mdo C Nogueira CM Ferreira VF Azeredo RB 《Magnetic resonance in chemistry : MRC》2008,46(12):1158-1162
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). 相似文献
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Pinto Pablo B. da Cruz Kimberly C. T. da Silva Júnior Eufrânio N. Cury Luiz A. 《Journal of fluorescence》2022,32(4):1299-1308
Journal of Fluorescence - Dropcast films produced from blends solutions of phenazine 1,2,3-triazole molecules in very low concentrations in a 1,3-Bis (N-carbazolyl) benzene (mCP) matrix... 相似文献
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Hernández DM de Moura MA Valencia DP González FJ González I de Abreu FC da Silva Júnior EN Ferreira VF Pinto AV Goulart MO Frontana C 《Organic & biomolecular chemistry》2008,6(18):3414-3420
In this work, the electrochemical behaviour of an antitumoral nitro o-quinone derivative obtained from 3-bromo-nor-beta-lapachone was studied. Cyclic voltammetric experiments, in acetonitrile solution, revealed that both quinone and nitro functions are reduced independently as quasi-reversible one-electron transfer processes in this order. Depending on the reduction potential, a radical anion or a biradical dianion is obtained. The formation of these paramagnetic species was confirmed by performing in situ Electrochemical-Electron Spin Resonance (E-ESR) experiments. Analysis of the kinetics of electron transfer associated to those electron uptake processes, in terms of the Marcus-Hush-Levich model, revealed differences in the reorganization energy (lambda((k))) for both steps (lambda((I)): 1.07-1.11 eV; lambda((II)): 1.21-1.30 eV). By evaluating the conformations of the radical and biradical systems by calculations at the BLYP//TZVP level of theory, it was found that the inner component, for the second reduction process (lambda((II))) was approximately 72% of lambda((II)), reflecting modifications in the molecular structure during the radical anion-biradical dianion transition. This change is also reflected in the differences presented by line widths of the ESR signals of both electrogenerated radical and diradical species. 相似文献
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Prof. Dr. Eufrânio N. da Silva Júnior Renato L. de Carvalho Renata G. Almeida Luisa G. Rosa Dr. Felipe Fantuzzi Dr. Torben Rogge Pedro M. S. Costa Prof. Dr. Claudia Pessoa Prof. Dr. Claus Jacob Prof. Dr. Lutz Ackermann 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(48):10981-10986
Double ruthenium(II)-catalyzed alkyne annulations of quinones were accomplished. Thus, a strategy is reported that provides step-economical access to valuable quinones with a wide range of applications. C−H/N−H activations for alkyne annulations of naphthoquinones provided challenging polycyclic quinoidal compounds by forming four new bonds in one step. The singular power of the thus-obtained compounds was reflected by their antileukemic activity. 相似文献
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Oliveira LG Silva MM Paula FC Pereira-Maia EC Donnici CL Simone CA Frézard F Silva EN Demicheli C 《Molecules (Basel, Switzerland)》2011,16(12):10314-10323
Antimony(V) and bismuth(V) complexes of lapachol have been synthesized by the reaction of Ph?SbCl? or Ph?BiCl? with lapachol (Lp) and characterized by several physicochemical techniques such as IR, and NMR spectroscopy and X-ray crystallography. The compounds contain six-coordinated antimony and bismuth atoms. The antimony(V) complex is a monomeric derivative, (Lp)(Ph?Sb)OH, and the bismuth(V) complex is a dinuclear compound bridged by an oxygen atom, (Lp)?(Ph?Bi)?O. Both compounds inhibited the growth of a chronic myelogenous leukemia cell line and the complex of Bi(V) was about five times more active than free lapachol. This work provides a rare example of an organo-Bi(V) complex showing significant cytotoxic activity. 相似文献
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Emilay B. T. Diogo Dr. Fábio G. Delolo Gabriela A. P. Graça Esther R. S. Paz Ícaro A. O. Bozzi Prof. Dr. Renata Diniz Juliano P. Passos Prof. Dr. Tulio Matencio Dr. Liane K. Soares Prof. Dr. Diego Alves Pedro M. S. Costa Prof. Dr. Claudia Pessoa Prof. Dr. Cynthia L. M. Pereira Prof. Dr. Lutz Ackermann Prof. Dr. Eufrânio N. da Silva Júnior 《European journal of organic chemistry》2023,26(38):e202300506
Undivided electrochemical cells enable economical preparation of sulphur-containing naphthoquinones through electrochemical sulphenylation of quinoidal compounds. The environmentally friendly and efficient protocol eliminates the use of chemical oxidants and facilitates the synthesis of the desired molecules. This approach offers an efficient and versatile method to synthesize quinones that exhibit cytotoxicity against cancer cell lines. 相似文献
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