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[:pb]Crystal Structure of the Chiral Azomethine Imine, (Z)-(S)-4-(tert-Butylcarbonylamino)-2-(2-methoxybenzylidene)-5-oxopyrazolidin-2-ium-1-ide, Obtained by the Cyclization of tert-Butyl (S)-2-[2-(methoxybenzylidene)hydrazine]-1-(hydroxymethyl)-2-oxocarbamate[:]

[:pb]Authors: Pinheiro, A. C.; De Souza, M. V. N.; Wardell, S. M. S. V.; Wardell, J. L. Source: Journal of Chemical Crystallography, v. 1, p. 1-8, 2018 Publisher: Springer Abstract Further study of the cyclization reactions of (S)-t-BuOCH2CONHCH(CH2OH)CONHN = Ar, derived from (L)-serine, has found that reaction with MeI/K2CO3 in Me2CO produces (Z)-(S)-4-(tert-butylcarbonylamino)-2-(benzylidene)-5-oxopyrazolidin-2-ium-1-ide, 3. We now wish to report […]

[:pb]Crystal structures and Hirshfeld surfaces of four methoxybenzaldehyde oxime derivatives, 2-MeO- C H C=NOH ( = H and 2-, 3- and 4-MeO): different conformations and hydrogen-bonding patterns[:]

[:pb]Authors: Gomes, L. R.; De Souza, M. V. N.; Da Costa, C. F.; Wardell, J. L.; Low, J. N. Source: Acta Crystallographica Section e, Crystallographic Communications, v. 74, p. 1553-1560, 2018 Publisher: Crystallographic Communications Abstract The crystal structures of four (E)-meth­oxy­benzaldehyde oxime derivatives, namely (2-meth­oxy­benzaldehyde oxime, 1, 2,3-di­meth­oxy­benzaldehyde oxime, 2, 4-di­meth­oxy­benzaldehyde oxime, 3, and 2,5-di­meth­oxy­benzaldehyde oxime, 4, are discussed. The arrangements of […]

[:pb]Different classical hydrogen-bonding patterns in three salicylaldoxime derivatives, 2-HO-4- C H C=NOH ( = Me, OH and MeO)[:]

[:pb]Authors: Gomes, L. R.; De Souza, M. V. N.; Da Costa, C. F.; Wardell, J. L.; Low, J. N. Source: Acta Crystallographica Section e, Crystallographic Communications, v. 74, p. 1480-1485, 2018 Publisher: Science Direct Abstract The crystal structures of three salicyaldoxime compounds, namely 2-hy­droxy-4-methyl­benzaldehyde oxime, C8H9NO2, 1, 2,4-di­hydroxy­benzaldehyde oxime, C7H7NO3, 2, and 2-hy­droxy-4-meth­oxy­benzaldehyde oxime, C8H9NO3, 3, are discussed. […]

[:pb]Activity of mefloquine and mefloquine derivatives against Echinococcus multilocularis[:]

[:pb]Authors: Rufener, R.; Ritler, D.; Zielinski, J.; Dick, L.; Da Silva, E. T.; Araujo, A. S.; Joekel, D. E.; Czock, D.; Goepfert, C.; Moraes, A. M.; De Souza, M. V. N.; Müller, J.; Mevissen, M.; Hemphill, A.; Lundström-Stadelmann, B. Source: International Journal for Parasitology-Drugs and Drug Resistance, v. 8, p. 331-340, 2018 Publisher: Science Direct Abstract The cestode E. […]

[:pb]Synthesis, biological activity, and mechanism of action of 2-pyrazyl and pyridylhydrazone derivatives, new classes of antileishmanial agentes[:]

[:pb]Authors: De Souza, M. V. N.; Coimbra, E. S.; Antinarelli, L. M. R.; Crispi, M. A.; Nogueira, T. C. M.; Pinheiro, A. C. Source: ChemMedChem, v. 13, p. 1387-1394, 2018 Publisher: European Chemical Society Publishing Abstract In this work, we report the antileishmanial activity of 23 compounds based on 2-pyrazyl and 2-pyridylhydrazone derivatives. The compounds were tested against […]

[:pb]Eco-Friendly and Highly Efficient Multigram Synthesis of N-(2-Hydroxyethyl)-2-Oxo-2H-Chromene-3-Carboxamide as a Useful Intermediate Using Sonochemistry[:]

[:pb]Authors: Pinto, L.; De Souza, M. V. N. Source: Current Green Chemistry, v. 05, p. 104-107, 2018 Publisher: Bentham Science Abstract This study describes a new, simple and efficient process for the preparation of N-(2- hydroxyethyl)-2-oxo-2H-chromene-3-carboxamide, on a multigram scale (0.38 moles), by using ultrasound irradiation as green chemistry method. Optimal conditions and yield (83%) […]

[:pb]Expected and unexpected products of reactions of 2-hydrazinylbenzothiazole with 3-nitrobenzenesulfonyl chloride in different solventes[:]

[:pb]Authors: Morscher, A.; De Souza, M. V. N.; Wardell, J. L.; Harrison, W. T. A. Source: Acta Crystallographica Section e, Crystallographic Communications, v. 74, p. 673-677, 2018 Publisher: Science Direct Abstract The syntheses and crystal structures of 2-[2-(propan-2-yl­idene)hydrazin­yl]-1,3-benzo­thia­zol-3-ium 3-nitro­benzene­sulfonate (C10H12N2S+·C6H4NO5S−), (I), 2-[2-(3-nitro­benzene­sulfon­yl)hydrazin­yl]-1,3-benzo­thia­zole (C13H10N4O4S2), (II) and 2-[2-(3-nitro­benzene­sulfon­yl)hydrazin­yl]-1,3-benzo­thia­zol-3-ium 3-nitro­benzene­sulfonate (C13H11N4O4S2+·C6H4NO5S−), (III) are reported. Salt (I) arose from […]

[:pb]Multicomponent Reactions in the Synthesis of Complex Fused Coumarin Derivatives[:]

[:pb]Authors: Pinto, L. S. S.; Couri, M. R. C.; De Souza, M. V. N. Source: Current Organic Synthesis, v. 15, p. 21-37, 2018 Publisher: Bentham Science Abstract Background: Coumarin is an important class of natural products with applications in different areas of knowledge. Due to its importance, several methodologies and strategies have been developed for […]