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Artigo de periodico
Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction (2022)
Darbem, Mariana P; Esteves, Henrique A; Burrow, Robert A ; Paulino, Antonio Augusto Soares ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: RSC Advances. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
DARBEM, Mariana P et al. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, v. 12, p. 2145–2149, 2022Tradução . . Disponível em: https://doi.org/10.1039/d1ra08388k. Acesso em: 17 nov. 2024.
APA
Darbem, M. P., Esteves, H. A., Burrow, R. A., Paulino, A. A. S., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, 12, 2145–2149. doi:10.1039/d1ra08388k
NLM
Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1039/d1ra08388k
Vancouver
Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1039/d1ra08388k
Artigo de periodico
Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution (2019)
Santos, Fabiano S; Zanotto, Gabriel M; Argomedo, Luiz M. Z; Darbem, Mariana P; Gonçalves, Paulo F. B; Stefani, Hélio Alexandre ; Rodembusch, Fabiano S
Source: Dyes and Pigments. Unidade: FCF
Subjects: SENSORES ÓPTICOS, SÍNTESE ORGÂNICA
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ABNT
SANTOS, Fabiano S et al. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, v. 165, p. 372-382, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.02.047. Acesso em: 17 nov. 2024.
APA
Santos, F. S., Zanotto, G. M., Argomedo, L. M. Z., Darbem, M. P., Gonçalves, P. F. B., Stefani, H. A., & Rodembusch, F. S. (2019). Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, 165, 372-382. doi:10.1016/j.dyepig.2019.02.047
NLM
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
Vancouver
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
Artigo de periodico
Synthesis of symmetrical biaryl compounds by homocoupling reaction (2019)
Vasconcelos, Stanley N. S; Reis, Joel S; Oliveira, Isadora M. de; Balfour, Michael N; Stefani, Hélio Alexandre
Source: Tetrahedron. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
VASCONCELOS, Stanley N. S et al. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, v. 75, p. 1865-1959, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2019.02.001. Acesso em: 17 nov. 2024.
APA
Vasconcelos, S. N. S., Reis, J. S., Oliveira, I. M. de, Balfour, M. N., & Stefani, H. A. (2019). Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, 75, 1865-1959. doi:10.1016/j.tet.2019.02.001
NLM
Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
Vancouver
Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
Artigo de periodico
Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction (2019)
Darbem, Mariana P; Esteves, C. Henrique A; Oliveira, Isadora M. de; Reis, Joel S; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: RSC Advances. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
DARBEM, Mariana P et al. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, v. 9, p. 9468–9474, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9ra00523d. Acesso em: 17 nov. 2024.
APA
Darbem, M. P., Esteves, C. H. A., Oliveira, I. M. de, Reis, J. S., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, 9, 9468–9474. doi:10.1039/c9ra00523d
NLM
Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1039/c9ra00523d
Vancouver
Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1039/c9ra00523d
Trabalho de evento-resumo
CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline (2019)
Ferraz, L. S; Oliveira, Isadora Maria de; Stefani, Hélio Alexandre ; Rodrigues, T
Source: Resumos. Conference titles: Reunião Anual da Federação de Sociedades de Biologia Experimental/FeSBE. Unidade: FCF
Subjects: COMPOSTOS ORGÂNICOS, SÍNTESE ORGÂNICA
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ABNT
FERRAZ, L. S et al. CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline. 2019, Anais.. São Paulo: FeSBE, 2019. Disponível em: http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf. Acesso em: 17 nov. 2024.
APA
Ferraz, L. S., Oliveira, I. M. de, Stefani, H. A., & Rodrigues, T. (2019). CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline. In Resumos. São Paulo: FeSBE. Recuperado de http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
NLM
Ferraz LS, Oliveira IM de, Stefani HA, Rodrigues T. CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline [Internet]. Resumos. 2019 ;[citado 2024 nov. 17 ] Available from: http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
Vancouver
Ferraz LS, Oliveira IM de, Stefani HA, Rodrigues T. CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline [Internet]. Resumos. 2019 ;[citado 2024 nov. 17 ] Available from: http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
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: 17 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. 17 ] 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. 17 ] 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: 17 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. 17 ] 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. 17 ] 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: 17 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. 17 ] 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. 17 ] Available from: https://doi.org/10.1007/s11030-017-9764-5
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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
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: 17 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. 17 ] 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. 17 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Artigo de periodico
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
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ABNT
VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 17 nov. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., 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. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajoc.201700154
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajoc.201700154
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: 17 nov. 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 nov. 17 ]
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 nov. 17 ]
Trabalho de evento-resumo
Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction (2017)
Oliveira, Isadora Maria de; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
OLIVEIRA, Isadora Maria de e STEFANI, Hélio Alexandre e MANARIN, Flávia. Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 17 nov. 2024.
APA
Oliveira, I. M. de, Stefani, H. A., & Manarin, F. (2017). Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Oliveira IM de, Stefani HA, Manarin F. Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Oliveira IM de, Stefani HA, Manarin F. Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 17 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. 17 ] 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. 17 ] Available from: https://doi.org/10.1039/c7nj01803g
Website
Uso de microrreatores aumenta eficiência da produção de medicamentos [Depoimento a Amanda Oliveira] (2015)
Palma, Mauri Sérgio Alves ; Stefani, Hélio Alexandre ; Parise Filho, Roberto
Unidade: FCF
Subjects: MEDICAMENTO (PRODUÇÃO), SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALMA, Mauri Sérgio Alves e STEFANI, Hélio Alexandre e PARISE FILHO, Roberto. Uso de microrreatores aumenta eficiência da produção de medicamentos [Depoimento a Amanda Oliveira]. . São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: http://www5.usp.br/92657. Acesso em: 17 nov. 2024. , 2015
APA
Palma, M. S. A., Stefani, H. A., & Parise Filho, R. (2015). Uso de microrreatores aumenta eficiência da produção de medicamentos [Depoimento a Amanda Oliveira]. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Recuperado de http://www5.usp.br/92657
NLM
Palma MSA, Stefani HA, Parise Filho R. Uso de microrreatores aumenta eficiência da produção de medicamentos [Depoimento a Amanda Oliveira] [Internet]. 2015 ;[citado 2024 nov. 17 ] Available from: http://www5.usp.br/92657
Vancouver
Palma MSA, Stefani HA, Parise Filho R. Uso de microrreatores aumenta eficiência da produção de medicamentos [Depoimento a Amanda Oliveira] [Internet]. 2015 ;[citado 2024 nov. 17 ] Available from: http://www5.usp.br/92657
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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] 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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.5935/0103-5053.20150114
Artigo de periodico
Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement (2015)
Souza, Frederico B; Shamim, Anwar; Argomedo, Luiz M. Z; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Frederico B et al. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, v. 19, n. 4, p. 773-785, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9619-x. Acesso em: 17 nov. 2024.
APA
Souza, F. B., Shamim, A., Argomedo, L. M. Z., Pimenta, D. C., & Stefani, H. A. (2015). Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, 19( 4), 773-785. doi:10.1007/s11030-015-9619-x
NLM
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
Vancouver
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.5935/0103-5053.20150038

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