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Artigo de periodico
Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum (2019)
Vasconcelos, Stanley Nunes Siqueira ; Meissner, Kamila Anna ; Ferraz, Witor R.; Trossini, Gustavo Henrique Goulart ; Wrenger, Carsten ; Stefani, Hélio Alexandre
Source: Future Medicinal Chemistry. Unidades: FCF, ICB
Subjects: MALÁRIA, PLASMODIUM FALCIPARUM, PROTOZOA, ANTIMALÁRICOS, ANIMAIS PARASITOS, VIRULÊNCIA
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum. Future Medicinal Chemistry, v. 11, n. 6, p. 525-538, 2019Tradução . . Disponível em: https://doi.org/10.4155/fmc-2018-0246. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Meissner, K. A., Ferraz, W. R., Trossini, G. H. G., Wrenger, C., & Stefani, H. A. (2019). Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum. Future Medicinal Chemistry, 11( 6), 525-538. doi:10.4155/fmc-2018-0246
NLM
Vasconcelos SNS, Meissner KA, Ferraz WR, Trossini GHG, Wrenger C, Stefani HA. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum [Internet]. Future Medicinal Chemistry. 2019 ; 11( 6): 525-538.[citado 2024 abr. 23 ] Available from: https://doi.org/10.4155/fmc-2018-0246
Vancouver
Vasconcelos SNS, Meissner KA, Ferraz WR, Trossini GHG, Wrenger C, Stefani HA. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum [Internet]. Future Medicinal Chemistry. 2019 ; 11( 6): 525-538.[citado 2024 abr. 23 ] Available from: https://doi.org/10.4155/fmc-2018-0246
Artigo de periodico
Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones (2019)
Vasconcelos, Stanley Nunes Siqueira ; Oliveira, Isadora Maria de ; Shamim, Anwar ; Zukerman-Schpector, Júlio ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC
Subjects: ALDEÍDOS, ESTEREOQUÍMICA
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Pimenta, D. C., & Stefani, H. A. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564
NLM
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/adsc.201900564
Vancouver
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/adsc.201900564
Artigo de periodico
Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells (2018)
Vasconcelos, Stanley Nunes Siqueira ; Sciani, Juliana Mozer ; Lisboa, Nicole Mambeli; Stefani, Hélio Alexandre
Source: Medicinal Chemistry. Unidade: FCF
Subjects: MOLÉCULA, ANTINEOPLÁSICOS
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, v. 14, n. 7, p. 709-714, 2018Tradução . . Disponível em: https://doi.org/10.2174/1573406414666180309153142. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Sciani, J. M., Lisboa, N. M., & Stefani, H. A. (2018). Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, 14( 7), 709-714. doi:10.2174/1573406414666180309153142
NLM
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 abr. 23 ] Available from: https://doi.org/10.2174/1573406414666180309153142
Vancouver
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 abr. 23 ] Available from: https://doi.org/10.2174/1573406414666180309153142
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: 23 abr. 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 abr. 23 ] 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 abr. 23 ] Available from: https://doi.org/10.1055/s-0036-1589090
Artigo de periodico
Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells (2017)
Ali, Bakat; Kupa, Léonard de Vinci Kanda; Heluany, Cíntia Scucuglia; Drewes, Carine Cristiane; Vasconcelos, Stanley Nunes Siqueira; Farsky, Sandra Helena Poliselli ; Stefani, Hélio Alexandre
Source: Bioorganic Chemistry. Unidade: FCF
Subjects: CÉLULAS EPITELIAIS, CÉLULAS-TRONCO
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ABNT
ALI, Bakat et al. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells. Bioorganic Chemistry, v. 72, p. 199-207, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2017.04.013. Acesso em: 23 abr. 2024.
APA
Ali, B., Kupa, L. de V. K., Heluany, C. S., Drewes, C. C., Vasconcelos, S. N. S., Farsky, S. H. P., & Stefani, H. A. (2017). Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells. Bioorganic Chemistry, 72, 199-207. doi:10.1016/j.bioorg.2017.04.013
NLM
Ali B, Kupa L de VK, Heluany CS, Drewes CC, Vasconcelos SNS, Farsky SHP, Stefani HA. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells [Internet]. Bioorganic Chemistry. 2017 ; 72 199-207.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.bioorg.2017.04.013
Vancouver
Ali B, Kupa L de VK, Heluany CS, Drewes CC, Vasconcelos SNS, Farsky SHP, Stefani HA. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells [Internet]. Bioorganic Chemistry. 2017 ; 72 199-207.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.bioorg.2017.04.013
Tese (Doutorado)
Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias (2017)
Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre (Orientador)
Unidade: FCF
Subjects: INSUMOS FARMACÊUTICOS, FLUORESCÊNCIA, ANTIMALÁRICOS, CÉLULAS
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ABNT
VASCONCELOS, Stanley Nunes Siqueira. Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias. 2017. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2017. Disponível em: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S. (2017). Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/
NLM
Vasconcelos SNS. Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias [Internet]. 2017 ;[citado 2024 abr. 23 ] Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/
Vancouver
Vasconcelos SNS. Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias [Internet]. 2017 ;[citado 2024 abr. 23 ] Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/
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: 23 abr. 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 abr. 23 ] 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 abr. 23 ] Available from: https://doi.org/10.1002/slct.201701197
Artigo de periodico
Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization (2017)
Shamim, Anwar; Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, COBRE
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ABNT
SHAMIM, Anwar et al. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, v. 58, n. 9, p. 884-888, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.059. Acesso em: 23 abr. 2024.
APA
Shamim, A., Souza, F. B. de, Vasconcelos, S. N. S., & Stefani, H. A. (2017). Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, 58( 9), 884-888. doi:10.1016/j.tetlet.2017.01.059
NLM
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Vancouver
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Trabalho de evento-resumo
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley Nunes Siqueira; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Abstracts. Conference titles: Tetrahedron Symposium - New Development in Organic Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. 2017, Anais.. Budapest: Elsevier, 2017. . Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. In Abstracts. Budapest: Elsevier.
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;[citado 2024 abr. 23 ]
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;[citado 2024 abr. 23 ]
Artigo de periodico
Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition (2017)
Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, COBRE
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ABNT
SOUZA, Frederico Bernardes de et al. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, v. 58, n. 11, p. 1057-1060, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.107. Acesso em: 23 abr. 2024.
APA
Souza, F. B. de, Vasconcelos, S. N. S., Reis, J. S. dos, Pimenta, D. C., & Stefani, H. A. (2017). Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, 58( 11), 1057-1060. doi:10.1016/j.tetlet.2017.01.107
NLM
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
Vancouver
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
Artigo de periodico
Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives (2016)
Vasconcelos, Stanley Nunes Siqueira; Rodrigues, Ana Clara Beltran; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Source: Chemistry Select. Unidades: IQ, FCF
Subjects: FLUORESCÊNCIA, PEPTÍDEOS
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives. Chemistry Select, v. 1, n. 6, p. 1287-1291, 2016Tradução . . Disponível em: https://doi.org/10.1002/slct.201600319. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Rodrigues, A. C. B., Bastos, E. L., & Stefani, H. A. (2016). Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives. Chemistry Select, 1( 6), 1287-1291. doi:10.1002/slct.201600319
NLM
Vasconcelos SNS, Rodrigues ACB, Bastos EL, Stefani HA. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives [Internet]. Chemistry Select. 2016 ; 1( 6): 1287-1291.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/slct.201600319
Vancouver
Vasconcelos SNS, Rodrigues ACB, Bastos EL, Stefani HA. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives [Internet]. Chemistry Select. 2016 ; 1( 6): 1287-1291.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/slct.201600319
Artigo de periodico
Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine (2016)
Vasconcelos, Stanley Nunes Siqueira; Shamim, Anwar; Ali, Bakhat; Oliveira, Isadora M. de; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: PEPTÍDEOS, TIROXINA
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, v. 20, n. 2, p. 469-481, 2016Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9642-y. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Shamim, A., Ali, B., Oliveira, I. M. de, & Stefani, H. A. (2016). Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, 20( 2), 469-481. doi:10.1007/s11030-015-9642-y
NLM
Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
Vancouver
Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
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: 23 abr. 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 abr. 23 ] 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 abr. 23 ] Available from: https://doi.org/10.1002/slct.201601526
Artigo de periodico
Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines (2016)
Vasconcelos, Stanley Nunes Siqueira; Drewes, Carine C; Kupa, Leonard de Vinci Kanda; Farsky, Sandra Helena Poliselli ; Stefani, Hélio Alexandre
Source: European Journal of Medicinal Chemistry. Unidade: FCF
Assunto: MELANOMA
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines. European Journal of Medicinal Chemistry, v. 114, p. 1-7, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2016.02.062. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Drewes, C. C., Kupa, L. de V. K., Farsky, S. H. P., & Stefani, H. A. (2016). Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines. European Journal of Medicinal Chemistry, 114, 1-7. doi:10.1016/j.ejmech.2016.02.062
NLM
Vasconcelos SNS, Drewes CC, Kupa L de VK, Farsky SHP, Stefani HA. Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines [Internet]. European Journal of Medicinal Chemistry. 2016 ; 114 1-7.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.ejmech.2016.02.062
Vancouver
Vasconcelos SNS, Drewes CC, Kupa L de VK, Farsky SHP, Stefani HA. Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines [Internet]. European Journal of Medicinal Chemistry. 2016 ; 114 1-7.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.ejmech.2016.02.062
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 abr. 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 abr. 23 ] 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 abr. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Artigo de periodico
Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones (2015)
Ali, Bakhat; Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALI, Bakhat et al. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, v. 56, n. 28, p. 4234-4241, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.05.066. Acesso em: 23 abr. 2024.
APA
Ali, B., Shamim, A., Vasconcelos, S. N. S., & Stefani, H. A. (2015). Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, 56( 28), 4234-4241. doi:10.1016/j.tetlet.2015.05.066
NLM
Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
Vancouver
Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
Artigo de periodico
Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters (2015)
Khan, Amna N; Vasconcelos, Stanley Nunes Siqueira; Carrau, Gonzalo; Stefani, Hélio Alexandre
Source: Journal of the Brazilian Chemical Society. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, AMINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KHAN, Amna N et al. Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters. Journal of the Brazilian Chemical Society, v. 26, n. 7, p. 1457-1465, 2015Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20150114. Acesso em: 23 abr. 2024.
APA
Khan, A. N., Vasconcelos, S. N. S., Carrau, G., & Stefani, H. A. (2015). Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters. Journal of the Brazilian Chemical Society, 26( 7), 1457-1465. doi:10.5935/0103-5053.20150114
NLM
Khan AN, Vasconcelos SNS, Carrau G, Stefani HA. Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 7): 1457-1465.[citado 2024 abr. 23 ] Available from: https://doi.org/10.5935/0103-5053.20150114
Vancouver
Khan AN, Vasconcelos SNS, Carrau G, Stefani HA. Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 7): 1457-1465.[citado 2024 abr. 23 ] Available from: https://doi.org/10.5935/0103-5053.20150114
Artigo de periodico
Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts (2015)
Vasconcelos, Stanley Nunes Siqueira; Barbeiro, Cristiane S; Khan, Amna N; Stefani, Hélio Alexandre
Source: Journal of the Braziliam Chemical Society. Unidade: FCF
Subjects: QUÍMICA FARMACÊUTICA, BORO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts. Journal of the Braziliam Chemical Society, v. 26, n. 4, p. 765-774, 2015Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20150038. Acesso em: 23 abr. 2024.
APA
Vasconcelos, S. N. S., Barbeiro, C. S., Khan, A. N., & Stefani, H. A. (2015). Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts. Journal of the Braziliam Chemical Society, 26( 4), 765-774. doi:10.5935/0103-5053.20150038
NLM
Vasconcelos SNS, Barbeiro CS, Khan AN, Stefani HA. Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts [Internet]. Journal of the Braziliam Chemical Society. 2015 ; 26( 4): 765-774.[citado 2024 abr. 23 ] Available from: https://doi.org/10.5935/0103-5053.20150038
Vancouver
Vasconcelos SNS, Barbeiro CS, Khan AN, Stefani HA. Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts [Internet]. Journal of the Braziliam Chemical Society. 2015 ; 26( 4): 765-774.[citado 2024 abr. 23 ] Available from: https://doi.org/10.5935/0103-5053.20150038
Artigo de periodico
Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters (2014)
Stefani, Hélio Alexandre ; Manarin, Flávia; Khan, Amna N; Vasconcelos, Stanley Nunes Siqueira
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: ITÉRBIO, BORO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, v. 6, p. 1236-1240, 2014Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201301421. Acesso em: 23 abr. 2024.
APA
Stefani, H. A., Manarin, F., Khan, A. N., & Vasconcelos, S. N. S. (2014). Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, 6, 1236-1240. doi:10.1002/ejoc.201301421
NLM
Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ejoc.201301421
Vancouver
Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ejoc.201301421
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 abr. 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 abr. 23 ] 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 abr. 23 ] Available from: https://doi.org/10.3390/molecules19021990

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