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Thio analogs of pyrimidine bases: Syntheses and EIMS study of new ortho-( meta- and para-)bromobenzyl s-mono and S-N-1-disubstituted 5-morpholinomethyl(5-piperidinomethyl)-2-thiouracils.
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- Journal of Heterocyclic Chemistry, 2007, v. 44, n. 1, p. 55, doi. 10.1002/jhet.5570440109
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- Article
JMS Letters.
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- Journal of Mass Spectrometry, 2012, v. 47, n. 3, p. 347, doi. 10.1002/jms.2976
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- Article
EI MS and ESI MS studies of the bisesquiterpene from cotton seeds-Gossypol and its Aza-derivatives.
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- Journal of Mass Spectrometry, 2008, v. 43, n. 5, p. 680, doi. 10.1002/jms.1371
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- Article
Design and Synthesis of New Bile AcidSterol Conjugates Linked via 1,2,3-Triazole Ring.
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- Helvetica Chimica Acta, 2015, v. 98, n. 10, p. 1337, doi. 10.1002/hlca.201500118
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- Article
Electron Impact and Electrospray Mass Spectral Study of ZnCl<sub>2</sub> Complexes with Nicotinoids.
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- Croatica Chemica Acta, 2018, v. 91, n. 1, p. 115, doi. 10.5562/cca3244
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- Article
Electron ionization induced mass spectral study of new isomeric 2- o-( m- and p-)nitrobenzylthio-5-piperidinomethyl(morpholinomethyl)uracils and 1,2-di- o-( m- and p-)nitrobenzyl-5-piperidinomethyl(morpholinomethyl)-2-thiouracils.
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- Rapid Communications in Mass Spectrometry: RCM, 2006, v. 20, n. 4, p. 713, doi. 10.1002/rcm.2338
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- Article
Electron impact mass spectral study of 1,2-di- o-( m- and p-)nitro-(bromo-)benzyl-2-thio-6-methyluracils and 1,2-di- o-( m- and p-)nitro-(bromo-)benzyl-2-thio-5-bromo-6-methyluracils.
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- Rapid Communications in Mass Spectrometry: RCM, 2005, v. 19, n. 4, p. 580, doi. 10.1002/rcm.1801
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- Article
Synthesis, antioxidant and cytoprotective activity evaluation of C-3 substituted indole derivatives.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-94904-z
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- Article
Thio Analogs of Pyrimidine Bases: Synthesis, Spectroscopic Study, and In Silico Biological Activity Evaluation of New 2-o-(m- and p-) Chlorobenzylthio-6-Methyl-5-Piperidino- (Morpholino-)Methyluracils.
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- ISRN Organic Chemistry, 2011, p. 1, doi. 10.5402/2011/610521
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- Article
Mass Spectrometry Study of New Polyamine Derivatives of Caffeine.
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- Acta Chimica Slovenica, 2018, v. 65, n. 4, p. 795, doi. 10.17344/acsi.2018.4339
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- Article
Spectroscopic Methods and Theoretical Studies of Bromoacetyl Substituted Derivatives of Bile Acids.
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- Acta Chimica Slovenica, 2015, v. 62, n. 1, p. 15, doi. 10.17344/acsi.2014.608
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- Article
Mass Spectrometry of Bis-quinolizidine Alkaloids: Unexpected Dimerization in Electron Ionization Mass Spectrometry.
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- Acta Chimica Slovenica, 2013, v. 60, n. 4, p. 833
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- Article
Synthesis, Structure, Surface and Antimicrobial Properties of New Oligomeric Quaternary Ammonium Salts with Aromatic Spacers.
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- Molecules, 2017, v. 22, n. 11, p. 1810, doi. 10.3390/molecules22111810
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- Article
Quaternary Alkylammonium Conjugates of Steroids: Synthesis, Molecular Structure, and Biological Studies.
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- Molecules, 2015, v. 20, n. 11, p. 20887, doi. 10.3390/molecules201119735
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Synthesis, Spectroscopic and Theoretical Studies of New Dimeric Quaternary Alkylammonium Conjugates of Sterols.
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- Molecules, 2014, v. 19, n. 7, p. 9419, doi. 10.3390/molecules19079419
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- Article
Synthesis, Spectroscopic and Theoretical Studies of New Quaternary N,N-Dimethyl-3-phthalimidopropylammonium Conjugates of Sterols and Bile Acid.
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- Molecules, 2014, v. 19, n. 4, p. 4212, doi. 10.3390/molecules19044212
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- Article
Synthesis, Spectroscopic and Theoretical Studies of New Quasi-Podands from Bile Acid Derivatives Linked by 1,2,3-Triazole Rings.
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- Molecules, 2014, v. 19, n. 2, p. 2557, doi. 10.3390/molecules19022557
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Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols.
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- Molecules, 2013, v. 18, n. 12, p. 14961, doi. 10.3390/molecules181214961
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Heteroatoms and π electrons as favorable factors for efficient corrosion protection.
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- Materials & Corrosion / Werkstoffe und Korrosion, 2019, v. 70, n. 6, p. 1099, doi. 10.1002/maco.201810570
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Maria Skłodowska-Curie - the first lady of nuclear physics.
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- Journal of Contemporary Brachytherapy, 2019, v. 11, n. 6, p. 505, doi. 10.5114/jcb.2019.91221
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- Article