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Artigo de periodico
The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil (2023)
Penteado, André Berndt ; Ribeiro, Geovani de Oliveira ; Araújo, Emerson Luiz Lima ; Kato, Rodrigo Bentes; Freire, Caio César de Melo ; Araújo, Joselio Maria Galvão de; Wallau, Gabriel da Luz; Salvato, Richard Steiner; Jesus, Ronaldo de; Bosco, Geraldine Goes ; Franz, Helena Ferreira; Silva, Pedro Eduardo Almeida da; Elcio de Souza Leal; Trossini, Gustavo Henrique Goulart ; Lima Neto, Daniel Ferreira de
Source: Research Square. Unidades: FFCLRP, FCF
Subjects: DENGUE, FILOGENIA
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ABNT
PENTEADO, André Berndt et al. The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil. Research Square, 2023Tradução . . Disponível em: https://doi.org/10.21203/rs.3.rs-3121559/v1. Acesso em: 07 nov. 2024.
APA
Penteado, A. B., Ribeiro, G. de O., Araújo, E. L. L., Kato, R. B., Freire, C. C. de M., Araújo, J. M. G. de, et al. (2023). The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil. Research Square. doi:10.21203/rs.3.rs-3121559/v1
NLM
Penteado AB, Ribeiro G de O, Araújo ELL, Kato RB, Freire CC de M, Araújo JMG de, Wallau G da L, Salvato RS, Jesus R de, Bosco GG, Franz HF, Silva PEA da, Elcio de Souza Leal, Trossini GHG, Lima Neto DF de. The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil [Internet]. Research Square. 2023 ;[citado 2024 nov. 07 ] Available from: https://doi.org/10.21203/rs.3.rs-3121559/v1
Vancouver
Penteado AB, Ribeiro G de O, Araújo ELL, Kato RB, Freire CC de M, Araújo JMG de, Wallau G da L, Salvato RS, Jesus R de, Bosco GG, Franz HF, Silva PEA da, Elcio de Souza Leal, Trossini GHG, Lima Neto DF de. The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil [Internet]. Research Square. 2023 ;[citado 2024 nov. 07 ] Available from: https://doi.org/10.21203/rs.3.rs-3121559/v1
Artigo de periodico
Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling (2018)
Oliveira, Isadora Maria de; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: New Journal of Chemistry. Unidade: FCF
Subjects: SELÊNIO, ESTEREOQUÍMICA
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ABNT
OLIVEIRA, Isadora Maria de et al. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, v. 42, n. 12, p. 10118-10123, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8nj01543k. Acesso em: 07 nov. 2024.
APA
Oliveira, I. M. de, Pimenta, D. C., Zukerman-Schpector, J., Stefani, H. A., & Manarin, F. (2018). Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, 42( 12), 10118-10123. doi:10.1039/c8nj01543k
NLM
Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1039/c8nj01543k
Vancouver
Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1039/c8nj01543k
Artigo de periodico
Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted (2018)
Oliveira, Isadora M. de; Darbem, Mariana P; Esteves, Carlos Henrique Alves; Pimenta, Daniel C; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: Tetrahedron Letters. Unidade: FCF
Subjects: ITÉRBIO, SÍNTESE ORGÂNICA
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, v. 59, n. 24, p. 3907-3911, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.09.022. Acesso em: 07 nov. 2024.
APA
Oliveira, I. M. de, Darbem, M. P., Esteves, C. H. A., Pimenta, D. C., Schpector, J. Z., Stefani, H. A., & Manarin, F. (2018). Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, 59( 24), 3907-3911. doi:10.1016/j.tetlet.2018.09.022
NLM
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Vancouver
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Artigo de periodico
Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Synthesis. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 07 nov. 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
NLM
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1055/s-0036-1589090
Vancouver
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1055/s-0036-1589090
Artigo de periodico
Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles (2017)
Vasconcelos, Stanley N. S; Fornari, Evelin; Caracelli, Ignez; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: ALFA-AMINOÁCIDOS, SÍNTESE ORGÂNICA
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ABNT
VASCONCELOS, Stanley N. S et al. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles. Molecular Diversity, v. 21, n. 4, p. 893-902, 2017Tradução . . Disponível em: https://doi.org/10.1007/s11030-017-9764-5. Acesso em: 07 nov. 2024.
APA
Vasconcelos, S. N. S., Fornari, E., Caracelli, I., & Stefani, H. A. (2017). Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles. Molecular Diversity, 21( 4), 893-902. doi:10.1007/s11030-017-9764-5
NLM
Vasconcelos SNS, Fornari E, Caracelli I, Stefani HA. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles [Internet]. Molecular Diversity. 2017 ; 21( 4): 893-902.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1007/s11030-017-9764-5
Vancouver
Vasconcelos SNS, Fornari E, Caracelli I, Stefani HA. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles [Internet]. Molecular Diversity. 2017 ; 21( 4): 893-902.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1007/s11030-017-9764-5
Artigo de periodico
Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines (2017)
Barbeiro, Cristiane de Souza; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Zukerman-Schpector, Júlio; Caracelli, Ignez; Maganhi, Stella Hernandez; Stefani, Hélio Alexandre
Source: ChemistrySelect. Unidade: FCF
Subjects: PALÁDIO, QUÍMICA FARMACÊUTICA
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ABNT
BARBEIRO, Cristiane de Souza et al. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, v. 2, n. 26, p. 8173-8177, 2017Tradução . . Disponível em: https://doi.org/10.1002/slct.201701197. Acesso em: 07 nov. 2024.
APA
Barbeiro, C. de S., Vasconcelos, S. N. S., Oliveira, I. M. de, Zukerman-Schpector, J., Caracelli, I., Maganhi, S. H., & Stefani, H. A. (2017). Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, 2( 26), 8173-8177. doi:10.1002/slct.201701197
NLM
Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/slct.201701197
Vancouver
Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/slct.201701197
Artigo de periodico
Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles (2017)
Ali, Bakhat; Vasconcelos, Stanley N. S; Shamim, Anwar; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre
Source: Arabian Journal of Chemistry. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS
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ABNT
ALI, Bakhat et al. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, v. 10, n. 4, p. 500-508, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.06.003. Acesso em: 07 nov. 2024.
APA
Ali, B., Vasconcelos, S. N. S., Shamim, A., Schpector, J. Z., & Stefani, H. A. (2017). Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, 10( 4), 500-508. doi:10.1016/j.arabjc.2016.06.003
NLM
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Vancouver
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Artigo de periodico
Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines (2017)
Oliveira, Isadora M. de; Vasconcelos, Stanley S. N; Barbeiro, Cristiane S; Correra, Thiago Carita ; Shamim, Anwar; Pimenta, Daniel Carvalho; Caracelli, Ignez; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: New Journal of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 07 nov. 2024.
APA
Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g
NLM
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1039/c7nj01803g
Vancouver
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1039/c7nj01803g
Artigo de periodico
Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis (2016)
Schpector, Júlio Zukerman; Madureira, Lucas Sousa; Stefani, Hélio Alexandre ; Gozhina, Olga; Tiekink, Edward R. T
Source: Zeitschrift fur Kristallographie. Unidade: FCF
Subjects: DIFRAÇÃO POR RAIOS X, CRISTALOGRAFIA ESTRUTURAL
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ABNT
SCHPECTOR, Júlio Zukerman et al. Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis. Zeitschrift fur Kristallographie, v. 231, n. 6, p. 329-339, 2016Tradução . . Disponível em: https://doi.org/10.1515/zkri-2015-1911. Acesso em: 07 nov. 2024.
APA
Schpector, J. Z., Madureira, L. S., Stefani, H. A., Gozhina, O., & Tiekink, E. R. T. (2016). Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis. Zeitschrift fur Kristallographie, 231( 6), 329-339. doi:10.1515/zkri-2015-1911
NLM
Schpector JZ, Madureira LS, Stefani HA, Gozhina O, Tiekink ERT. Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis [Internet]. Zeitschrift fur Kristallographie. 2016 ; 231( 6): 329-339.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1515/zkri-2015-1911
Vancouver
Schpector JZ, Madureira LS, Stefani HA, Gozhina O, Tiekink ERT. Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis [Internet]. Zeitschrift fur Kristallographie. 2016 ; 231( 6): 329-339.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1515/zkri-2015-1911
Artigo de periodico
Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties (2016)
Barbeiro, Cristiane S; Vasconcelos, Stanley Nunes Siqueira; Schpector, Júlio Zukerman; Caracelli, Ignez; Pimenta, Daniel C; Rodrigues, Ana Clara Beltran; Fernandes, André S; Correra, Thiago Carita ; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Source: ChemistrySelect. Unidades: IQ, FCF
Subjects: MECANISMOS, FLUORESCÊNCIA
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ABNT
BARBEIRO, Cristiane S et al. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, v. 2, p. 5647–5652, 2016Tradução . . Disponível em: https://doi.org/10.1002/slct.201601526. Acesso em: 07 nov. 2024.
APA
Barbeiro, C. S., Vasconcelos, S. N. S., Schpector, J. Z., Caracelli, I., Pimenta, D. C., Rodrigues, A. C. B., et al. (2016). Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, 2, 5647–5652. doi:10.1002/slct.201601526
NLM
Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/slct.201601526
Vancouver
Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/slct.201601526
Artigo de periodico
Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound (2016)
Caracelli, Ignez; Zukerman-Schpector, Júlio; Madureira, Lucas Sousa; Maganhi, Stella Hernandez; Stefani, Hélio Alexandre ; Guadagnin, Rafael C; Tiekink, Edward R. T
Source: Zeitschrift fur Kristallographie - Crystalline Materials. Unidade: FCF
Subjects: DIFRAÇÃO POR RAIOS X, COMPOSTOS ORGÂNICOS
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ABNT
CARACELLI, Ignez et al. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound. Zeitschrift fur Kristallographie - Crystalline Materials, v. 231, n. 6, p. 321–328, 2016Tradução . . Disponível em: https://doi.org/10.1515/zkri-2016-1931. Acesso em: 07 nov. 2024.
APA
Caracelli, I., Zukerman-Schpector, J., Madureira, L. S., Maganhi, S. H., Stefani, H. A., Guadagnin, R. C., & Tiekink, E. R. T. (2016). Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound. Zeitschrift fur Kristallographie - Crystalline Materials, 231( 6), 321–328. doi:10.1515/zkri-2016-1931
NLM
Caracelli I, Zukerman-Schpector J, Madureira LS, Maganhi SH, Stefani HA, Guadagnin RC, Tiekink ERT. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound [Internet]. Zeitschrift fur Kristallographie - Crystalline Materials. 2016 ; 231( 6): 321–328.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1515/zkri-2016-1931
Vancouver
Caracelli I, Zukerman-Schpector J, Madureira LS, Maganhi SH, Stefani HA, Guadagnin RC, Tiekink ERT. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound [Internet]. Zeitschrift fur Kristallographie - Crystalline Materials. 2016 ; 231( 6): 321–328.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1515/zkri-2016-1931
Artigo de periodico
Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization (2015)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Ali, Bakhat; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO
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ABNT
SHAMIM, Anwar et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 07 nov. 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052
NLM
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Vancouver
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Artigo de periodico
Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes (2015)
Ali, Bakhat; Schpector, Júlio Zukerman; Ferreira, Fernando P; Shamim, Anwar; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: AMINAS, CATÁLISE
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ABNT
ALI, Bakhat et al. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, v. 56, n. 9, p. 1153-1158, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 07 nov. 2024.
APA
Ali, B., Schpector, J. Z., Ferreira, F. P., Shamim, A., Pimenta, D. C., & Stefani, H. A. (2015). Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, 56( 9), 1153-1158. doi:10.1016/j.tetlet.2015.01.059
NLM
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Vancouver
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Artigo de periodico
Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers (2014)
Schpector, Julio Zukermann; Madureira, Lucas Sousa; Wulf, Glaudeston Dutra; Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Ng, Seik Weng; Tiekink, Edward R. T
Source: Molecules. Unidade: FCF
Subjects: DIFRAÇÃO POR RAIOS X, SÍNTESE ORGÂNICA
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ABNT
SCHPECTOR, Julio Zukermann et al. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, v. 19, n. 2, p. 1990-2003, 2014Tradução . . Disponível em: https://doi.org/10.3390/molecules19021990. Acesso em: 07 nov. 2024.
APA
Schpector, J. Z., Madureira, L. S., Wulf, G. D., Stefani, H. A., Vasconcelos, S. N. S., Ng, S. W., & Tiekink, E. R. T. (2014). Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, 19( 2), 1990-2003. doi:10.3390/molecules19021990
NLM
Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 nov. 07 ] Available from: https://doi.org/10.3390/molecules19021990
Vancouver
Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 nov. 07 ] Available from: https://doi.org/10.3390/molecules19021990
Artigo de periodico
N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin (2013)
Maganhi, Stella Hernandez; Damião, Mariana Celestina Frojuello Bernstorff; Tavares, Maurício Temotheo; Parise Filho, Roberto
Source: Acta Crystallographica Section E. Unidade: FCF
Assunto: ANTINEOPLÁSICOS
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ABNT
MAGANHI, Stella Hernandez et al. N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin. Acta Crystallographica Section E, v. E69, p. 0332 : + Supplementary materials ( S1-S6), 2013Tradução . . Disponível em: https://doi.org/10.1107/S1600536813002201. Acesso em: 07 nov. 2024.
APA
Maganhi, S. H., Damião, M. C. F. B., Tavares, M. T., & Parise Filho, R. (2013). N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin. Acta Crystallographica Section E, E69, 0332 : + Supplementary materials ( S1-S6). doi:10.1107/S1600536813002201
NLM
Maganhi SH, Damião MCFB, Tavares MT, Parise Filho R. N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin [Internet]. Acta Crystallographica Section E. 2013 ; E69 0332 : + Supplementary materials ( S1-S6).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1107/S1600536813002201
Vancouver
Maganhi SH, Damião MCFB, Tavares MT, Parise Filho R. N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin [Internet]. Acta Crystallographica Section E. 2013 ; E69 0332 : + Supplementary materials ( S1-S6).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1107/S1600536813002201
Artigo de periodico
Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction (2013)
Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Manarin, Flávia; Leal, Daiana Martins; Souza, Frederico B; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Eberlin, Marcos Nogueira; Godoi, Marla N; Galaverna, Renan de Souza
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: COMPOSTOS HETEROCÍCLICOS, TELÚRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction. European Journal of Organic Chemistry, n. 18, p. 3780-3783, 2013Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201300009. Acesso em: 07 nov. 2024.
APA
Stefani, H. A., Vasconcelos, S. N. S., Manarin, F., Leal, D. M., Souza, F. B., Madureira, L. S., et al. (2013). Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction. European Journal of Organic Chemistry, ( 18), 3780-3783. doi:10.1002/ejoc.201300009
NLM
Stefani HA, Vasconcelos SNS, Manarin F, Leal DM, Souza FB, Madureira LS, Zukerman-Schpector J, Eberlin MN, Godoi MN, Galaverna R de S. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction [Internet]. European Journal of Organic Chemistry. 2013 ;( 18): 3780-3783.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ejoc.201300009
Vancouver
Stefani HA, Vasconcelos SNS, Manarin F, Leal DM, Souza FB, Madureira LS, Zukerman-Schpector J, Eberlin MN, Godoi MN, Galaverna R de S. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction [Internet]. European Journal of Organic Chemistry. 2013 ;( 18): 3780-3783.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ejoc.201300009
Artigo de periodico
One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles (2013)
Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Souza, Frederico B; Manarin, Flávia; Zukerman-Schpector, Júlio
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, v. 54, n. 43, p. 5821-5825, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.064. Acesso em: 07 nov. 2024.
APA
Stefani, H. A., Vasconcelos, S. N. S., Souza, F. B., Manarin, F., & Zukerman-Schpector, J. (2013). One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, 54( 43), 5821-5825. doi:10.1016/j.tetlet.2013.08.064
NLM
Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
Vancouver
Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
Artigo de periodico
N-[(1,3-Benzodioxol-5-yl)methyl]- benzenesulfonamide: an analogue of capsaicin (2013)
Maganhi, Stella Hernandez; Tavares, Maurício Temotheo; Damião, Mariana C. F. C. B; Parise Filho, Roberto
Source: Acta Crystallographica Section E. Unidade: FCF
Subjects: ANTINEOPLÁSICOS, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAGANHI, Stella Hernandez et al. N-[(1,3-Benzodioxol-5-yl)methyl]- benzenesulfonamide: an analogue of capsaicin. Acta Crystallographica Section E, p. o1700 : + Supplementary materials (S1-S6), 2013Tradução . . Disponível em: https://doi.org/10.1107/S1600536813028481. Acesso em: 07 nov. 2024.
APA
Maganhi, S. H., Tavares, M. T., Damião, M. C. F. C. B., & Parise Filho, R. (2013). N-[(1,3-Benzodioxol-5-yl)methyl]- benzenesulfonamide: an analogue of capsaicin. Acta Crystallographica Section E, o1700 : + Supplementary materials (S1-S6). doi:10.1107/S1600536813028481
NLM
Maganhi SH, Tavares MT, Damião MCFCB, Parise Filho R. N-[(1,3-Benzodioxol-5-yl)methyl]- benzenesulfonamide: an analogue of capsaicin [Internet]. Acta Crystallographica Section E. 2013 ; o1700 : + Supplementary materials (S1-S6).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1107/S1600536813028481
Vancouver
Maganhi SH, Tavares MT, Damião MCFCB, Parise Filho R. N-[(1,3-Benzodioxol-5-yl)methyl]- benzenesulfonamide: an analogue of capsaicin [Internet]. Acta Crystallographica Section E. 2013 ; o1700 : + Supplementary materials (S1-S6).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1107/S1600536813028481
Artigo de periodico
Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction (2012)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Manarin, Flávia; Lüdtke, Diogo, Seibert; Zukerman-Schpector, Júlio; Madureira, Lucas Sousa; Tiekink, Edward R. T
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, v. 53, n. 14, p. 1742-1747 : + Supplementary materials ( S1-S36), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.01.102. Acesso em: 07 nov. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Manarin, F., Lüdtke, D., Zukerman-Schpector, J., Madureira, L. S., & Tiekink, E. R. T. (2012). Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, 53( 14), 1742-1747 : + Supplementary materials ( S1-S36). doi:10.1016/j.tetlet.2012.01.102
NLM
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Vancouver
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Artigo de periodico
Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives (2012)
Stefani, Hélio Alexandre ; Botteselle, Giancarlo Di Vaccari; Zukerman-Schpector, Júlio; Caracelli, Ignez; Corrêa, Denis da Silva; Farsky, Sandra Helena Poliselli ; Machado, Isabel Daufenback; Santin, José Roberto; Hebeda, Cristina Bichels
Source: European Journal of Medicinal Chemistry. Unidade: FCF
Subjects: AMINOÁCIDOS, ANTI-INFLAMATÓRIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives. European Journal of Medicinal Chemistry, v. 47, n. 1, p. 52-58 : + Supplementary materials ( S1-S6), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2011.10.018. Acesso em: 07 nov. 2024.
APA
Stefani, H. A., Botteselle, G. D. V., Zukerman-Schpector, J., Caracelli, I., Corrêa, D. da S., Farsky, S. H. P., et al. (2012). Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives. European Journal of Medicinal Chemistry, 47( 1), 52-58 : + Supplementary materials ( S1-S6). doi:10.1016/j.ejmech.2011.10.018
NLM
Stefani HA, Botteselle GDV, Zukerman-Schpector J, Caracelli I, Corrêa D da S, Farsky SHP, Machado ID, Santin JR, Hebeda CB. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives [Internet]. European Journal of Medicinal Chemistry. 2012 ; 47( 1): 52-58 : + Supplementary materials ( S1-S6).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.ejmech.2011.10.018
Vancouver
Stefani HA, Botteselle GDV, Zukerman-Schpector J, Caracelli I, Corrêa D da S, Farsky SHP, Machado ID, Santin JR, Hebeda CB. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives [Internet]. European Journal of Medicinal Chemistry. 2012 ; 47( 1): 52-58 : + Supplementary materials ( S1-S6).[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.ejmech.2011.10.018

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