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Artigo de periodico
Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry (2023)
Borges, Letícia da Silva; Batista, João Henrique Carvalho; Bozzini, Leandro Alves ; Lourenço Júnior, Celso Donizete; Lopes, Norberto Peporine ; Clososki, Giuliano Cesar ; Vessecchi, Ricardo
Source: Rapid Communications in Mass Spectrometry. Unidades: FCFRP, FFCLRP
Subjects: ÍONS, MECÂNICA QUÂNTICA, ESPECTROMETRIA DE MASSAS
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ABNT
BORGES, Letícia da Silva et al. Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry. Rapid Communications in Mass Spectrometry, v. 37, n. 4, p. 1-11, 2023Tradução . . Disponível em: https://doi.org/10.1002/rcm.9449. Acesso em: 19 nov. 2024.
APA
Borges, L. da S., Batista, J. H. C., Bozzini, L. A., Lourenço Júnior, C. D., Lopes, N. P., Clososki, G. C., & Vessecchi, R. (2023). Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry. Rapid Communications in Mass Spectrometry, 37( 4), 1-11. doi:10.1002/rcm.9449
NLM
Borges L da S, Batista JHC, Bozzini LA, Lourenço Júnior CD, Lopes NP, Clososki GC, Vessecchi R. Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry [Internet]. Rapid Communications in Mass Spectrometry. 2023 ; 37( 4): 1-11.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/rcm.9449
Vancouver
Borges L da S, Batista JHC, Bozzini LA, Lourenço Júnior CD, Lopes NP, Clososki GC, Vessecchi R. Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry [Internet]. Rapid Communications in Mass Spectrometry. 2023 ; 37( 4): 1-11.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/rcm.9449
Artigo de periodico
Preparation of activated charcoal from Acrocomia aculeata for purification of pretreated crude glycerol (2022)
Barbosa, Sandro L.; Freitas, Milton S. de; Santos, Wallans T. P. dos; Nelson, David Lee; Marques, Maria Betânia de Freitas; Klein, Stanlei I.; Clososki, Giuliano Cesar ; Caires, Franco Jazon ; Nassar, Eduardo J.; Zanatta, Lucas D.; Agblevor, Foster A.; Afonso, Carlos A. M.; Baroni, Adriano C. Moraes
Source: Biomass Conversion and Biorefinery. Unidade: FCFRP
Subjects: CARVÃO ATIVADO, MACAÚBA, BIODIESEL, ADSORÇÃO, COMPOSTOS ORGÂNICOS
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BARBOSA, Sandro L. et al. Preparation of activated charcoal from Acrocomia aculeata for purification of pretreated crude glycerol. Biomass Conversion and Biorefinery, v. 12, n. 7, p. 2441-2449, 2022Tradução . . Disponível em: https://doi.org/10.1007/s13399-020-00745-7. Acesso em: 19 nov. 2024.
APA
Barbosa, S. L., Freitas, M. S. de, Santos, W. T. P. dos, Nelson, D. L., Marques, M. B. de F., Klein, S. I., et al. (2022). Preparation of activated charcoal from Acrocomia aculeata for purification of pretreated crude glycerol. Biomass Conversion and Biorefinery, 12( 7), 2441-2449. doi:10.1007/s13399-020-00745-7
NLM
Barbosa SL, Freitas MS de, Santos WTP dos, Nelson DL, Marques MB de F, Klein SI, Clososki GC, Caires FJ, Nassar EJ, Zanatta LD, Agblevor FA, Afonso CAM, Baroni ACM. Preparation of activated charcoal from Acrocomia aculeata for purification of pretreated crude glycerol [Internet]. Biomass Conversion and Biorefinery. 2022 ; 12( 7): 2441-2449.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s13399-020-00745-7
Vancouver
Barbosa SL, Freitas MS de, Santos WTP dos, Nelson DL, Marques MB de F, Klein SI, Clososki GC, Caires FJ, Nassar EJ, Zanatta LD, Agblevor FA, Afonso CAM, Baroni ACM. Preparation of activated charcoal from Acrocomia aculeata for purification of pretreated crude glycerol [Internet]. Biomass Conversion and Biorefinery. 2022 ; 12( 7): 2441-2449.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s13399-020-00745-7
Artigo de periodico
Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines (2022)
Bertallo, Camila Rodrigues de Souza ; Berlim, Leonardo S.; Olivier, Danilo S.; Arroio, Thais Rodrigues ; Ito, Amando Siuiti ; Clososki, Giuliano Cesar
Source: Dyes and Pigments. Unidades: FFCLRP, FCFRP
Subjects: FÍSICO-QUÍMICA, COMPOSIÇÃO QUÍMICA
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BERTALLO, Camila Rodrigues de Souza et al. Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines. Dyes and Pigments, v. 198, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2021.109996. Acesso em: 19 nov. 2024.
APA
Bertallo, C. R. de S., Berlim, L. S., Olivier, D. S., Arroio, T. R., Ito, A. S., & Clososki, G. C. (2022). Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines. Dyes and Pigments, 198. doi:10.1016/j.dyepig.2021.109996
NLM
Bertallo CR de S, Berlim LS, Olivier DS, Arroio TR, Ito AS, Clososki GC. Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines [Internet]. Dyes and Pigments. 2022 ; 198[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109996
Vancouver
Bertallo CR de S, Berlim LS, Olivier DS, Arroio TR, Ito AS, Clososki GC. Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines [Internet]. Dyes and Pigments. 2022 ; 198[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109996
Artigo de periodico
Catalytic transformation of triglycerides to biodiesel with SiO2-SO3H and quaternary ammonium salts in toluene or DMSO (2022)
Barbosa, Sandro L.; Rocha, Adeline C. Pereira; Nelson, David Lee; Freitas, Milton S. de; Mestre, Antônio A. P. Fulgêncio; Klein, Stanlei I.; Clososki, Giuliano Cesar ; Caires, Franco Jazon ; Flumignan, Danilo L.; Santos, Letícia Karen dos; Wentz, Alexandre P.; Pasa, Vânya M. Duarte; Rios, Regiane D. Fernandes
Source: Molecules. Unidade: FCFRP
Subjects: BIODIESEL, CATÁLISE, CATALISADORES, ÁCIDOS GRAXOS
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ABNT
BARBOSA, Sandro L. et al. Catalytic transformation of triglycerides to biodiesel with SiO2-SO3H and quaternary ammonium salts in toluene or DMSO. Molecules, v. 27, n. 3, p. 1-13, 2022Tradução . . Disponível em: https://doi.org/10.3390/molecules27030953. Acesso em: 19 nov. 2024.
APA
Barbosa, S. L., Rocha, A. C. P., Nelson, D. L., Freitas, M. S. de, Mestre, A. A. P. F., Klein, S. I., et al. (2022). Catalytic transformation of triglycerides to biodiesel with SiO2-SO3H and quaternary ammonium salts in toluene or DMSO. Molecules, 27( 3), 1-13. doi:10.3390/molecules27030953
NLM
Barbosa SL, Rocha ACP, Nelson DL, Freitas MS de, Mestre AAPF, Klein SI, Clososki GC, Caires FJ, Flumignan DL, Santos LK dos, Wentz AP, Pasa VMD, Rios RDF. Catalytic transformation of triglycerides to biodiesel with SiO2-SO3H and quaternary ammonium salts in toluene or DMSO [Internet]. Molecules. 2022 ; 27( 3): 1-13.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/molecules27030953
Vancouver
Barbosa SL, Rocha ACP, Nelson DL, Freitas MS de, Mestre AAPF, Klein SI, Clososki GC, Caires FJ, Flumignan DL, Santos LK dos, Wentz AP, Pasa VMD, Rios RDF. Catalytic transformation of triglycerides to biodiesel with SiO2-SO3H and quaternary ammonium salts in toluene or DMSO [Internet]. Molecules. 2022 ; 27( 3): 1-13.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/molecules27030953
Artigo de periodico
Efficient N-arylation of 4-chloroquinazolines en route to novel 4-anilinoquinazolines as potential anticancer agents (2021)
Nishimura, Rodolfo Hideki Vicente ; Santos, Thiago dos ; Murie, Valter Eduardo ; Furtado, Luciana Costa ; Costa-Lotufo, Letícia Veras ; Clososki, Giuliano Cesar
Source: Beilstein Journal of Organic Chemistry. Unidades: ICB, FCFRP
Subjects: FARMACOLOGIA, ANTINEOPLÁSICOS, TECNOLOGIA DE MICRO-ONDAS, ADENOSINA
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ABNT
NISHIMURA, Rodolfo Hideki Vicente et al. Efficient N-arylation of 4-chloroquinazolines en route to novel 4-anilinoquinazolines as potential anticancer agents. Beilstein Journal of Organic Chemistry, v. 17, p. 2968–2975, 2021Tradução . . Disponível em: https://doi.org/10.3762/bjoc.17.206. Acesso em: 19 nov. 2024.
APA
Nishimura, R. H. V., Santos, T. dos, Murie, V. E., Furtado, L. C., Costa-Lotufo, L. V., & Clososki, G. C. (2021). Efficient N-arylation of 4-chloroquinazolines en route to novel 4-anilinoquinazolines as potential anticancer agents. Beilstein Journal of Organic Chemistry, 17, 2968–2975. doi:10.3762/bjoc.17.206
NLM
Nishimura RHV, Santos T dos, Murie VE, Furtado LC, Costa-Lotufo LV, Clososki GC. Efficient N-arylation of 4-chloroquinazolines en route to novel 4-anilinoquinazolines as potential anticancer agents [Internet]. Beilstein Journal of Organic Chemistry. 2021 ; 17 2968–2975.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3762/bjoc.17.206
Vancouver
Nishimura RHV, Santos T dos, Murie VE, Furtado LC, Costa-Lotufo LV, Clososki GC. Efficient N-arylation of 4-chloroquinazolines en route to novel 4-anilinoquinazolines as potential anticancer agents [Internet]. Beilstein Journal of Organic Chemistry. 2021 ; 17 2968–2975.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3762/bjoc.17.206
Artigo de periodico
Recentes avanços na funcionalização seletiva de quinolinas (2021)
Ferreira, Dartagnan; Murie, Valter Eduardo ; Santos, Thiago dos ; Vieira, Paulo Cezar ; Clososki, Giuliano Cesar
Source: Química Nova. Unidade: FCFRP
Subjects: COMPOSTOS AROMÁTICOS, COMPOSTOS HETEROCÍCLICOS, LIGANTES
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FERREIRA, Dartagnan et al. Recentes avanços na funcionalização seletiva de quinolinas. Química Nova, v. 44, n. 5, p. 599-615, 2021Tradução . . Disponível em: https://doi.org/10.21577/0100-4042.20170701. Acesso em: 19 nov. 2024.
APA
Ferreira, D., Murie, V. E., Santos, T. dos, Vieira, P. C., & Clososki, G. C. (2021). Recentes avanços na funcionalização seletiva de quinolinas. Química Nova, 44( 5), 599-615. doi:10.21577/0100-4042.20170701
NLM
Ferreira D, Murie VE, Santos T dos, Vieira PC, Clososki GC. Recentes avanços na funcionalização seletiva de quinolinas [Internet]. Química Nova. 2021 ; 44( 5): 599-615.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0100-4042.20170701
Vancouver
Ferreira D, Murie VE, Santos T dos, Vieira PC, Clososki GC. Recentes avanços na funcionalização seletiva de quinolinas [Internet]. Química Nova. 2021 ; 44( 5): 599-615.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0100-4042.20170701
Artigo de periodico
Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents (2021)
Murie, Valter Eduardo ; Nicolino, Paula Valim ; Santos, Thiago dos ; Gambacorta, Guido ; Nishimura, Rodolfo Hideki Vicente ; Perovani, Icaro Salgado ; Furtado, Luciana Costa ; Costa-Lotufo, Letícia Veras ; Oliveira, Anderson Rodrigo Moraes de; Lourenço, Ricardo Vessecchi ; Baxendale, Ian R. ; Clososki, Giuliano Cesar
Source: The Journal of Organic Chemistry. Unidades: ICB, FFCLRP, FCFRP
Subjects: FARMACOLOGIA, ANTIOXIDANTES, REAGENTES, MAGNÉSIO, METAIS ALCALINOS, ELÉTRONS, COMPOSTOS AROMÁTICOS
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MURIE, Valter Eduardo et al. Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents. The Journal of Organic Chemistry, v. 86, n. 19, p. 13402-13419, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.1c01521. Acesso em: 19 nov. 2024.
APA
Murie, V. E., Nicolino, P. V., Santos, T. dos, Gambacorta, G., Nishimura, R. H. V., Perovani, I. S., et al. (2021). Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents. The Journal of Organic Chemistry, 86( 19), 13402-13419. doi:10.1021/acs.joc.1c01521
NLM
Murie VE, Nicolino PV, Santos T dos, Gambacorta G, Nishimura RHV, Perovani IS, Furtado LC, Costa-Lotufo LV, Oliveira ARM de, Lourenço RV, Baxendale IR, Clososki GC. Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 19): 13402-13419.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.joc.1c01521
Vancouver
Murie VE, Nicolino PV, Santos T dos, Gambacorta G, Nishimura RHV, Perovani IS, Furtado LC, Costa-Lotufo LV, Oliveira ARM de, Lourenço RV, Baxendale IR, Clososki GC. Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 19): 13402-13419.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.joc.1c01521
Artigo de periodico
Tenofovir disoproxil fumarate: new chemical developments and encouraging in vitro biological results for SARS-CoV-2 (2020)
Clososki, Giuliano Cesar ; Soldi, Rafael A.; Silva, Rodrigo Moreira da ; Guaratini, Thais; Lopes, Jose Norberto Callegari; Pereira, Pâmela Rodrigues Rosa; Lopes, João Luis Callegari ; Santos, Thiago dos ; Martins Júnior, Ronaldo Bragança; Costa, Cristina Santos da; Carvalho, Andreia Nogueira de ; Silva, Luis Lamberti Pinto da ; Arruda, Eurico ; Lopes, Norberto Peporine
Source: Journal of the Brazilian Chemical Society. Unidades: FCFRP, FMRP
Subjects: METABÓLITOS, COVID-19, ESPECTROSCOPIA INFRAVERMELHA, ESPECTROMETRIA DE MASSAS
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ABNT
CLOSOSKI, Giuliano Cesar et al. Tenofovir disoproxil fumarate: new chemical developments and encouraging in vitro biological results for SARS-CoV-2. Journal of the Brazilian Chemical Society, v. 31, n. 8, p. 1552-1556, 2020Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20200106. Acesso em: 19 nov. 2024.
APA
Clososki, G. C., Soldi, R. A., Silva, R. M. da, Guaratini, T., Lopes, J. N. C., Pereira, P. R. R., et al. (2020). Tenofovir disoproxil fumarate: new chemical developments and encouraging in vitro biological results for SARS-CoV-2. Journal of the Brazilian Chemical Society, 31( 8), 1552-1556. doi:10.21577/0103-5053.20200106
NLM
Clososki GC, Soldi RA, Silva RM da, Guaratini T, Lopes JNC, Pereira PRR, Lopes JLC, Santos T dos, Martins Júnior RB, Costa CS da, Carvalho AN de, Silva LLP da, Arruda E, Lopes NP. Tenofovir disoproxil fumarate: new chemical developments and encouraging in vitro biological results for SARS-CoV-2 [Internet]. Journal of the Brazilian Chemical Society. 2020 ; 31( 8): 1552-1556.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0103-5053.20200106
Vancouver
Clososki GC, Soldi RA, Silva RM da, Guaratini T, Lopes JNC, Pereira PRR, Lopes JLC, Santos T dos, Martins Júnior RB, Costa CS da, Carvalho AN de, Silva LLP da, Arruda E, Lopes NP. Tenofovir disoproxil fumarate: new chemical developments and encouraging in vitro biological results for SARS-CoV-2 [Internet]. Journal of the Brazilian Chemical Society. 2020 ; 31( 8): 1552-1556.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0103-5053.20200106
Artigo de periodico
Assessment of the electronic structure of a triruthenium acetate-pyridylnaphthalimide cluster (2020)
Mateus, Douglas Braz Gonçalves ; Souza, Sâmya da Silva; Silva, Ricardo Junior de Bacchi da; Batista, Ana Paula de Lima ; Cicolani, Renato Salviato ; Murie, Valter Eduardo ; Nishimura, Rodolfo Hideki Vicente ; Clososki, Giuliano Cesar ; Oliveira Filho, Antonio Gustavo Sampaio de ; Demets, Grégoire Jean-François ; Nikolaou, Sofia
Source: Journal of Photochemistry & Photobiology A : Chemistry. Unidades: FCFRP, FFCLRP
Subjects: RUTÊNIO, MODELAGEM MOLECULAR, SÍNTESE INORGÂNICA
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ABNT
MATEUS, Douglas Braz Gonçalves et al. Assessment of the electronic structure of a triruthenium acetate-pyridylnaphthalimide cluster. Journal of Photochemistry & Photobiology A : Chemistry, v. 391, p. 112361, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jphotochem.2020.112361. Acesso em: 19 nov. 2024.
APA
Mateus, D. B. G., Souza, S. da S., Silva, R. J. de B. da, Batista, A. P. de L., Cicolani, R. S., Murie, V. E., et al. (2020). Assessment of the electronic structure of a triruthenium acetate-pyridylnaphthalimide cluster. Journal of Photochemistry & Photobiology A : Chemistry, 391, 112361. doi:10.1016/j.jphotochem.2020.112361
NLM
Mateus DBG, Souza S da S, Silva RJ de B da, Batista AP de L, Cicolani RS, Murie VE, Nishimura RHV, Clososki GC, Oliveira Filho AGS de, Demets GJ-F, Nikolaou S. Assessment of the electronic structure of a triruthenium acetate-pyridylnaphthalimide cluster [Internet]. Journal of Photochemistry & Photobiology A : Chemistry. 2020 ; 391 112361.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.jphotochem.2020.112361
Vancouver
Mateus DBG, Souza S da S, Silva RJ de B da, Batista AP de L, Cicolani RS, Murie VE, Nishimura RHV, Clososki GC, Oliveira Filho AGS de, Demets GJ-F, Nikolaou S. Assessment of the electronic structure of a triruthenium acetate-pyridylnaphthalimide cluster [Internet]. Journal of Photochemistry & Photobiology A : Chemistry. 2020 ; 391 112361.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.jphotochem.2020.112361
Artigo de periodico
Oxygenated biofuels: synthesis of fatty acid solketal esters with a mixture of sulfonated silica and (Bu4N)(BF4) catalyst (2019)
Barbosa, Sandro L. ; Lima, Pamela Cristina; Santos, Wallans Torres Pio dos ; Klein, Stanlei Ivair ; Clososki, Giuliano Cesar ; Caires, Franco Jazon
Source: Catalysis Communications. Unidade: FCFRP
Subjects: CATALISADORES, GLICERÍDEOS, SÍNTESE QUÍMICA, ÁCIDOS GRAXOS
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ABNT
BARBOSA, Sandro L. et al. Oxygenated biofuels: synthesis of fatty acid solketal esters with a mixture of sulfonated silica and (Bu4N)(BF4) catalyst. Catalysis Communications, v. 120, p. 76-79, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.catcom.2018.12.005. Acesso em: 19 nov. 2024.
APA
Barbosa, S. L., Lima, P. C., Santos, W. T. P. dos, Klein, S. I., Clososki, G. C., & Caires, F. J. (2019). Oxygenated biofuels: synthesis of fatty acid solketal esters with a mixture of sulfonated silica and (Bu4N)(BF4) catalyst. Catalysis Communications, 120, 76-79. doi:10.1016/j.catcom.2018.12.005
NLM
Barbosa SL, Lima PC, Santos WTP dos, Klein SI, Clososki GC, Caires FJ. Oxygenated biofuels: synthesis of fatty acid solketal esters with a mixture of sulfonated silica and (Bu4N)(BF4) catalyst [Internet]. Catalysis Communications. 2019 ; 120 76-79.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.catcom.2018.12.005
Vancouver
Barbosa SL, Lima PC, Santos WTP dos, Klein SI, Clososki GC, Caires FJ. Oxygenated biofuels: synthesis of fatty acid solketal esters with a mixture of sulfonated silica and (Bu4N)(BF4) catalyst [Internet]. Catalysis Communications. 2019 ; 120 76-79.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.catcom.2018.12.005
Artigo de periodico
Characterization and in silico mutagenic assessment of a new betahistine degradation impurity (2019)
Mello, Murilo Belini Marcondes de ; Oliveira, Antonio A. F. de; Oliveira, Caroline L. de; Ultramari, Mariah A.; Gama, Fernando H. S.; Mascarello, Alessandra; Guimarães, Cristiano R. W.; Freitas, Miller N. de; Cunha, Carlos E.; Lourenço, Tiago C.; Ferreira, Fernanda P.; Lopes, João Luis Callegari ; Clososki, Giuliano Cesar
Source: Journal of the Brazilian Chemical Society. Unidade: FCFRP
Subjects: ESTABILIDADE DOS MEDICAMENTOS, ESPECTROMETRIA DE MASSAS, CROMATOGRAFIA LÍQUIDA, MEDICAMENTO
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ABNT
MELLO, Murilo Belini Marcondes de et al. Characterization and in silico mutagenic assessment of a new betahistine degradation impurity. Journal of the Brazilian Chemical Society, v. 30, n. 7, p. 1415-1424, 2019Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20190037. Acesso em: 19 nov. 2024.
APA
Mello, M. B. M. de, Oliveira, A. A. F. de, Oliveira, C. L. de, Ultramari, M. A., Gama, F. H. S., Mascarello, A., et al. (2019). Characterization and in silico mutagenic assessment of a new betahistine degradation impurity. Journal of the Brazilian Chemical Society, 30( 7), 1415-1424. doi:10.21577/0103-5053.20190037
NLM
Mello MBM de, Oliveira AAF de, Oliveira CL de, Ultramari MA, Gama FHS, Mascarello A, Guimarães CRW, Freitas MN de, Cunha CE, Lourenço TC, Ferreira FP, Lopes JLC, Clososki GC. Characterization and in silico mutagenic assessment of a new betahistine degradation impurity [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 7): 1415-1424.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0103-5053.20190037
Vancouver
Mello MBM de, Oliveira AAF de, Oliveira CL de, Ultramari MA, Gama FHS, Mascarello A, Guimarães CRW, Freitas MN de, Cunha CE, Lourenço TC, Ferreira FP, Lopes JLC, Clososki GC. Characterization and in silico mutagenic assessment of a new betahistine degradation impurity [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 7): 1415-1424.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0103-5053.20190037
Artigo de periodico
Synthesis of phenyl esters using SiO2–SO3H catalyst in conventional heating and microwave-irradiated esterification processes (2019)
Barbosa, Sandro L.; Ottone, Myrlene; Freitas, Milton de S.; Lima, Camila D.; Nelson, David L.; Clososki, Giuliano Cesar ; Caires, Franco Jazon ; Klein, Stanlei I.; Hurtado, Gabriela R.
Source: Journal of Nanoscience and Nanotechnology. Unidades: FCFRP, FFCLRP
Subjects: CATALISADORES, TECNOLOGIA DE MICRO-ONDAS, ESTERIFICAÇÃO, ÁCIDOS CARBOXÍLICOS
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ABNT
BARBOSA, Sandro L. et al. Synthesis of phenyl esters using SiO2–SO3H catalyst in conventional heating and microwave-irradiated esterification processes. Journal of Nanoscience and Nanotechnology, v. 19, n. 6, p. 3663-3668, 2019Tradução . . Disponível em: https://doi.org/10.1166/jnn.2019.16104. Acesso em: 19 nov. 2024.
APA
Barbosa, S. L., Ottone, M., Freitas, M. de S., Lima, C. D., Nelson, D. L., Clososki, G. C., et al. (2019). Synthesis of phenyl esters using SiO2–SO3H catalyst in conventional heating and microwave-irradiated esterification processes. Journal of Nanoscience and Nanotechnology, 19( 6), 3663-3668. doi:10.1166/jnn.2019.16104
NLM
Barbosa SL, Ottone M, Freitas M de S, Lima CD, Nelson DL, Clososki GC, Caires FJ, Klein SI, Hurtado GR. Synthesis of phenyl esters using SiO2–SO3H catalyst in conventional heating and microwave-irradiated esterification processes [Internet]. Journal of Nanoscience and Nanotechnology. 2019 ; 19( 6): 3663-3668.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1166/jnn.2019.16104
Vancouver
Barbosa SL, Ottone M, Freitas M de S, Lima CD, Nelson DL, Clososki GC, Caires FJ, Klein SI, Hurtado GR. Synthesis of phenyl esters using SiO2–SO3H catalyst in conventional heating and microwave-irradiated esterification processes [Internet]. Journal of Nanoscience and Nanotechnology. 2019 ; 19( 6): 3663-3668.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1166/jnn.2019.16104
Artigo de periodico
The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study (2018)
Barbosa, Sandro L.; Lima, Camila D.; Almeida, Melina A. R.; Mourão, Larissa S.; Ottone, Myrlene; Nelson, David L.; Klein, Stanlei I.; Zanatta, Lucas D. ; Clososki, Giuliano Cesar ; Caires, Franco J. ; Nassar, Eduardo J.; Hurtado, Gabriela R.
Source: Heliyon. Unidades: FCFRP, FFCLRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, NIÓBIO, CARBONATOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, Sandro L. et al. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study. Heliyon, v. 4, n. 3, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2018.e00571. Acesso em: 19 nov. 2024.
APA
Barbosa, S. L., Lima, C. D., Almeida, M. A. R., Mourão, L. S., Ottone, M., Nelson, D. L., et al. (2018). The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study. Heliyon, 4( 3). doi:10.1016/j.heliyon.2018.e00571
NLM
Barbosa SL, Lima CD, Almeida MAR, Mourão LS, Ottone M, Nelson DL, Klein SI, Zanatta LD, Clososki GC, Caires FJ, Nassar EJ, Hurtado GR. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study [Internet]. Heliyon. 2018 ; 4( 3):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.heliyon.2018.e00571
Vancouver
Barbosa SL, Lima CD, Almeida MAR, Mourão LS, Ottone M, Nelson DL, Klein SI, Zanatta LD, Clososki GC, Caires FJ, Nassar EJ, Hurtado GR. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study [Internet]. Heliyon. 2018 ; 4( 3):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.heliyon.2018.e00571
Artigo de periodico
Ketalization of ketones to 1,3-dioxolanes and concurring self-aldolization catalyzed by an amorphous, hydrophilic SiO2-SO3H catalyst under microwave irradiation (2018)
Barbosa, Sandro L. ; Ottone, Myrlene; Almeida, Mainara T. de; Lage, Guilherme L. C.; Almeida, Melina A. R.; Nelson, David Lee; Santos, Wallans Torres Pio dos ; Clososki, Giuliano Cesar ; Lopes, Norberto Peporine ; Klein, Stanlei Ivair ; Zanatta, Lucas Dimarô
Source: Journal of the Brazilian Chemical Society. Unidades: FCFRP, FFCLRP
Subjects: CETONA, HIDRÓLISE, ÁCIDO SULFÚRICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, Sandro L. et al. Ketalization of ketones to 1,3-dioxolanes and concurring self-aldolization catalyzed by an amorphous, hydrophilic SiO2-SO3H catalyst under microwave irradiation. Journal of the Brazilian Chemical Society, v. 29, n. 8, p. 1663-1671, 2018Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20180039. Acesso em: 19 nov. 2024.
APA
Barbosa, S. L., Ottone, M., Almeida, M. T. de, Lage, G. L. C., Almeida, M. A. R., Nelson, D. L., et al. (2018). Ketalization of ketones to 1,3-dioxolanes and concurring self-aldolization catalyzed by an amorphous, hydrophilic SiO2-SO3H catalyst under microwave irradiation. Journal of the Brazilian Chemical Society, 29( 8), 1663-1671. doi:10.21577/0103-5053.20180039
NLM
Barbosa SL, Ottone M, Almeida MT de, Lage GLC, Almeida MAR, Nelson DL, Santos WTP dos, Clososki GC, Lopes NP, Klein SI, Zanatta LD. Ketalization of ketones to 1,3-dioxolanes and concurring self-aldolization catalyzed by an amorphous, hydrophilic SiO2-SO3H catalyst under microwave irradiation [Internet]. Journal of the Brazilian Chemical Society. 2018 ; 29( 8): 1663-1671.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0103-5053.20180039
Vancouver
Barbosa SL, Ottone M, Almeida MT de, Lage GLC, Almeida MAR, Nelson DL, Santos WTP dos, Clososki GC, Lopes NP, Klein SI, Zanatta LD. Ketalization of ketones to 1,3-dioxolanes and concurring self-aldolization catalyzed by an amorphous, hydrophilic SiO2-SO3H catalyst under microwave irradiation [Internet]. Journal of the Brazilian Chemical Society. 2018 ; 29( 8): 1663-1671.[citado 2024 nov. 19 ] Available from: https://doi.org/10.21577/0103-5053.20180039
Artigo de periodico
Base-controlled regioselective functionalization of chloro-substituted quinolines (2018)
Murie, Valter Eduardo ; Nishimura, Rodolfo Hideki Vicente ; Rolim, Larissa Araújo; Vessecchi, Ricardo ; Lopes, Norberto Peporine ; Clososki, Giuliano Cesar
Source: The Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP
Subjects: PRODUTOS NATURAIS, SÍNTESE ORGÂNICA, QUÍMICA MÉDICA, REAÇÕES QUÍMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MURIE, Valter Eduardo et al. Base-controlled regioselective functionalization of chloro-substituted quinolines. The Journal of Organic Chemistry, v. 83, n. 2, p. 871-880, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.7b02855. Acesso em: 19 nov. 2024.
APA
Murie, V. E., Nishimura, R. H. V., Rolim, L. A., Vessecchi, R., Lopes, N. P., & Clososki, G. C. (2018). Base-controlled regioselective functionalization of chloro-substituted quinolines. The Journal of Organic Chemistry, 83( 2), 871-880. doi:10.1021/acs.joc.7b02855
NLM
Murie VE, Nishimura RHV, Rolim LA, Vessecchi R, Lopes NP, Clososki GC. Base-controlled regioselective functionalization of chloro-substituted quinolines [Internet]. The Journal of Organic Chemistry. 2018 ; 83( 2): 871-880.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.joc.7b02855
Vancouver
Murie VE, Nishimura RHV, Rolim LA, Vessecchi R, Lopes NP, Clososki GC. Base-controlled regioselective functionalization of chloro-substituted quinolines [Internet]. The Journal of Organic Chemistry. 2018 ; 83( 2): 871-880.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.joc.7b02855
Artigo de periodico
Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast (2017)
Silva, Rafaela M.; Okano, Laura Tiemi; Rodrigues, J. Augusto R.; Clososki, Giuliano Cesar
Source: Tetrahedron : Asymmetry. Unidades: FCFRP, FFCLRP
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Rafaela M. et al. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast. Tetrahedron : Asymmetry, v. 28, p. 939-944, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2017.05.009. Acesso em: 19 nov. 2024.
APA
Silva, R. M., Okano, L. T., Rodrigues, J. A. R., & Clososki, G. C. (2017). Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast. Tetrahedron : Asymmetry, 28, 939-944. doi:10.1016/j.tetasy.2017.05.009
NLM
Silva RM, Okano LT, Rodrigues JAR, Clososki GC. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast [Internet]. Tetrahedron : Asymmetry. 2017 ; 28 939-944.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.tetasy.2017.05.009
Vancouver
Silva RM, Okano LT, Rodrigues JAR, Clososki GC. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast [Internet]. Tetrahedron : Asymmetry. 2017 ; 28 939-944.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.tetasy.2017.05.009
Artigo de periodico
Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever (2014)
Malvar, David do C.; Aguiar, Fernando A.; Vaz, Artur de L. L.; Assis, Débora C. R.; Melo, Miriam Cristina Contin de; Jabor, Valquíria A. P.; Kalapothakis, Evanguedes; Ferreira, Sérgio Henrique; Clososki, Giuliano Cesar; Souza, Glória Emília Petto de
Source: British Journal of Pharmacology. Unidade: FCFRP
Subjects: HIPOTERMIA, HIPOTÁLAMO, FARMACOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MALVAR, David do C. et al. Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever. British Journal of Pharmacology, v. 171, n. 15, p. 3666-3679, 2014Tradução . . Disponível em: https://doi.org/10.1111/bph.12717. Acesso em: 19 nov. 2024.
APA
Malvar, D. do C., Aguiar, F. A., Vaz, A. de L. L., Assis, D. C. R., Melo, M. C. C. de, Jabor, V. A. P., et al. (2014). Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever. British Journal of Pharmacology, 171( 15), 3666-3679. doi:10.1111/bph.12717
NLM
Malvar D do C, Aguiar FA, Vaz A de LL, Assis DCR, Melo MCC de, Jabor VAP, Kalapothakis E, Ferreira SH, Clososki GC, Souza GEP de. Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever [Internet]. British Journal of Pharmacology. 2014 ; 171( 15): 3666-3679.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1111/bph.12717
Vancouver
Malvar D do C, Aguiar FA, Vaz A de LL, Assis DCR, Melo MCC de, Jabor VAP, Kalapothakis E, Ferreira SH, Clososki GC, Souza GEP de. Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever [Internet]. British Journal of Pharmacology. 2014 ; 171( 15): 3666-3679.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1111/bph.12717

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