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Artigo de periodico
1-Iodoglycal: a versatile intermediate for the synthesis of D-Glyco amides and esters employing Carbonylative cross-coupling reaction (2024)
Hornink, Milene Macedo ; Toledo, Mônica Franco Zannini Junqueira ; Pimenta, Daniel Carvalho ; Paschoalin, Caio; Silva, Pamela M; Figlino, Giuseppe E; Aguiar, Eurípedes; Cervi, Gustavo ; Ribeiro, Francisco Wanderson Moreira; Correra, Thiago Carita ; Ferry, Angélique; Stefani, Hélio Alexandre
Source: ACS Omega. Unidades: FCF, IQ
Subjects: COMPOSTOS AROMÁTICOS, AMIDAS
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ABNT
HORNINK, Milene Macedo et al. 1-Iodoglycal: a versatile intermediate for the synthesis of D-Glyco amides and esters employing Carbonylative cross-coupling reaction. ACS Omega, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acsomega.4c02645. Acesso em: 05 out. 2024.
APA
Hornink, M. M., Toledo, M. F. Z. J., Pimenta, D. C., Paschoalin, C., Silva, P. M., Figlino, G. E., et al. (2024). 1-Iodoglycal: a versatile intermediate for the synthesis of D-Glyco amides and esters employing Carbonylative cross-coupling reaction. ACS Omega. doi:10.1021/acsomega.4c02645
NLM
Hornink MM, Toledo MFZJ, Pimenta DC, Paschoalin C, Silva PM, Figlino GE, Aguiar E, Cervi G, Ribeiro FWM, Correra TC, Ferry A, Stefani HA. 1-Iodoglycal: a versatile intermediate for the synthesis of D-Glyco amides and esters employing Carbonylative cross-coupling reaction [Internet]. ACS Omega. 2024 ;[citado 2024 out. 05 ] Available from: https://dx.doi.org/10.1021/acsomega.4c02645
Vancouver
Hornink MM, Toledo MFZJ, Pimenta DC, Paschoalin C, Silva PM, Figlino GE, Aguiar E, Cervi G, Ribeiro FWM, Correra TC, Ferry A, Stefani HA. 1-Iodoglycal: a versatile intermediate for the synthesis of D-Glyco amides and esters employing Carbonylative cross-coupling reaction [Internet]. ACS Omega. 2024 ;[citado 2024 out. 05 ] Available from: https://dx.doi.org/10.1021/acsomega.4c02645
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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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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1039/d1ra08388k
Artigo de periodico
Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals (2020)
Darbem, Mariana P; Esteves, Henrique A; Oliveira, Isadora Maria de ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: ChemCatChem. Unidades: BIOTECNOLOGIA, FCF, IQ
Subjects: PALÁDIO, HIDRÓLISE
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DARBEM, Mariana P et al. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, v. 12, n. 2, p. 576-583, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.201901403. Acesso em: 05 out. 2024.
APA
Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, Pimenta, D. C., & Stefani, H. A. (2020). Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, 12( 2), 576-583. doi:10.1002/cctc.201901403
NLM
Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 out. 05 ] Available from: https://doi.org/10.1002/cctc.201901403
Vancouver
Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 out. 05 ] Available from: https://doi.org/10.1002/cctc.201901403
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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1002/adsc.201900564
Artigo de periodico
Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides (2019)
Esteves, Henrique A; Darbem, Mariana P; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidades: BIOTECNOLOGIA, FCF
Subjects: MONÓXIDO DE CARBONO, PALÁDIO
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ABNT
ESTEVES, Henrique A et al. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, v. 2019, p. 7384-7388, 2019Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201901081. Acesso em: 05 out. 2024.
APA
Esteves, H. A., Darbem, M. P., Pimenta, D. C., & Stefani, H. A. (2019). Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, 2019, 7384-7388. doi:10.1002/ejoc.201901081
NLM
Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 out. 05 ] Available from: https://doi.org/10.1002/ejoc.201901081
Vancouver
Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 out. 05 ] Available from: https://doi.org/10.1002/ejoc.201901081
Artigo de periodico
Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization (2019)
Oliveira, Isadora M. de; Esteves, Carlos Henrique Alves ; Darbem, Mariana P; Pimenta, Daniel Carvalho ; Schpector, Júlio Zukerman ; Ferreira, Antônio Gilberto; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: Advanced Synthesis and Catalysis. Unidade: FCF
Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO
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ABNT
OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 05 out. 2024.
APA
Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142
NLM
Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 out. 05 ] Available from: https://doi.org/10.1002/adsc.201900142
Vancouver
Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 out. 05 ] Available from: https://doi.org/10.1002/adsc.201900142
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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1039/c8nj01543k
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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1055/s-0036-1589090
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: 05 out. 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 out. 05 ]
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 out. 05 ]
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: 05 out. 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 out. 05 ] 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 out. 05 ] 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
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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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1039/c7nj01803g
Artigo de periodico
Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles (2016)
Souza, Frederico B; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: TECNOLOGIA DE MICRO-ONDAS, ALDEÍDOS
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ABNT
SOUZA, Frederico B e PIMENTA, Daniel Carvalho e STEFANI, Hélio Alexandre. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, v. 57, n. 14, p. 1592-1596, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.02.105. Acesso em: 05 out. 2024.
APA
Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2016). Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, 57( 14), 1592-1596. doi:10.1016/j.tetlet.2016.02.105
NLM
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
Vancouver
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
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
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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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
Artigo de periodico
Synthesis of functionalized N-triazolyl maleimides (2014)
Stefani, Hélio Alexandre ; Ferreira, Fernando P; Ali, Bakhat; Pimenta, Daniel Carvalho
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, v. 55, n. 31, p. 4355-4358, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.05.095. Acesso em: 05 out. 2024.
APA
Stefani, H. A., Ferreira, F. P., Ali, B., & Pimenta, D. C. (2014). Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, 55( 31), 4355-4358. doi:10.1016/j.tetlet.2014.05.095
NLM
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Vancouver
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Artigo de periodico
Suzuki-Miyaura cross-coupling reactions of aryl tellurides with potassium aryltrifluoroborate salts (2006)
Cella, Rodrigo; Cunha, Rodrigo Luiz Oliveira Rodrigues; Reis, Ana E. S.; Pimenta, Daniel Carvalho; Klitzke, Clécio Fernando; Stefani, Hélio Alexandre
Source: Journal of Organic Chemistry. Unidade: FCF
Subjects: QUÍMICA FARMACÊUTICA, TELÚRIO, REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CELLA, Rodrigo et al. Suzuki-Miyaura cross-coupling reactions of aryl tellurides with potassium aryltrifluoroborate salts. Journal of Organic Chemistry, v. 70, n. 1, p. 244-250, 2006Tradução . . Acesso em: 05 out. 2024.
APA
Cella, R., Cunha, R. L. O. R., Reis, A. E. S., Pimenta, D. C., Klitzke, C. F., & Stefani, H. A. (2006). Suzuki-Miyaura cross-coupling reactions of aryl tellurides with potassium aryltrifluoroborate salts. Journal of Organic Chemistry, 70( 1), 244-250.
NLM
Cella R, Cunha RLOR, Reis AES, Pimenta DC, Klitzke CF, Stefani HA. Suzuki-Miyaura cross-coupling reactions of aryl tellurides with potassium aryltrifluoroborate salts. Journal of Organic Chemistry. 2006 ; 70( 1): 244-250.[citado 2024 out. 05 ]
Vancouver
Cella R, Cunha RLOR, Reis AES, Pimenta DC, Klitzke CF, Stefani HA. Suzuki-Miyaura cross-coupling reactions of aryl tellurides with potassium aryltrifluoroborate salts. Journal of Organic Chemistry. 2006 ; 70( 1): 244-250.[citado 2024 out. 05 ]

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