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Artigo de periodico
Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction (2022)
Jesus, Jéssica Carol de; Noguchi, Henrique Kenich ; Toledo, Mônica Franco Zannini Junqueira ; Burrow, Robert A ; Pimenta, Daniel C. ; Stefani, Hélio Alexandre
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: AMINOÁCIDOS, PROTEÍNAS, AMIDAS
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ABNT
JESUS, Jéssica Carol de et al. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, v. 2022, n. 30, p. 1-7 art. e202200332, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200332. Acesso em: 27 set. 2024.
APA
Jesus, J. C. de, Noguchi, H. K., Toledo, M. F. Z. J., Burrow, R. A., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, 2022( 30), 1-7 art. e202200332. doi:10.1002/ejoc.202200332
NLM
Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.202200332
Vancouver
Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.202200332
Artigo de periodico
Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals (2020)
Paulino, Antonio Augusto Soares ; Stefani, Hélio Alexandre
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: UREIA, PALÁDIO, GLICOCONJUGADOS
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ABNT
PAULINO, Antonio Augusto Soares e STEFANI, Hélio Alexandre. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 3847–3855, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000494. Acesso em: 27 set. 2024.
APA
Paulino, A. A. S., & Stefani, H. A. (2020). Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 3847–3855. doi:10.1002/ejoc.202000494
NLM
Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.202000494
Vancouver
Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.202000494
Artigo de periodico
α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals (2020)
Darbem, Mariana P; Esteves, Henrique A; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre
Fonte: European Journal of Organic Chemistry. Unidades: FCF, IQ
Assuntos: GLICOSÍDEOS, PALÁDIO
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ABNT
DARBEM, Mariana P et al. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 5220–5226, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000846. Acesso em: 27 set. 2024.
APA
Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, & Stefani, H. A. (2020). α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 5220–5226. doi:10.1002/ejoc.202000846
NLM
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.202000846
Vancouver
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.202000846
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
Fonte: ChemCatChem. Unidades: BIOTECNOLOGIA, FCF, IQ
Assuntos: PALÁDIO, HIDRÓLISE
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ABNT
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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1002/cctc.201901403
Artigo de periodico
Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers (2020)
Oliveira, Isadora Maria de ; Esteves, Henrique A; Darbem, Mariana P; Sartorelli, Arthur; Correra, Thiago Carita ; Oliveira, Andre F. Rodrigues ; Pimenta, Daniel C; Zukerman-Schpector, Júlio ; Stefani, Hélio Alexandre
Fonte: ChemCatChem. Unidades: FCF, IQ
Assuntos: LIGANTES, CATALISADORES
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ABNT
OLIVEIRA, Isadora Maria de et al. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, v. 12, p. 3545–3552, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.202000395. Acesso em: 27 set. 2024.
APA
Oliveira, I. M. de, Esteves, H. A., Darbem, M. P., Sartorelli, A., Correra, T. C., Oliveira, A. F. R., et al. (2020). Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, 12, 3545–3552. doi:10.1002/cctc.202000395
NLM
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/cctc.202000395
Vancouver
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/cctc.202000395
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
Fonte: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] 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
Fonte: European Journal of Organic Chemistry. Unidades: BIOTECNOLOGIA, FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] 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
Fonte: Advanced Synthesis and Catalysis. Unidade: FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1002/adsc.201900142
Artigo de periodico
Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) (2018)
Tornquist, Bruna Luisa; Bueno, Gabriel de Paula; Willig, Julia Caroline Manzano; Oliveira, Isadora Maria de; Stefani, Hélio Alexandre ; Rafique, Jamal; Saba, Sumbal; Iglesias, Bernardo Almeida; Botteselle, Giancarlo V; Manarin, Flávia
Fonte: ChemistrySelect. Unidade: FCF
Assuntos: ITÉRBIO, SÓDIO
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ABNT
TORNQUIST, Bruna Luisa et al. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs). ChemistrySelect, v. 3, p. 6358-6363, 2018Tradução . . Disponível em: https://doi.org/10.1002/slct.201800673. Acesso em: 27 set. 2024.
APA
Tornquist, B. L., Bueno, G. de P., Willig, J. C. M., Oliveira, I. M. de, Stefani, H. A., Rafique, J., et al. (2018). Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs). ChemistrySelect, 3, 6358-6363. doi:10.1002/slct.201800673
NLM
Tornquist BL, Bueno G de P, Willig JCM, Oliveira IM de, Stefani HA, Rafique J, Saba S, Iglesias BA, Botteselle GV, Manarin F. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) [Internet]. ChemistrySelect. 2018 ; 3 6358-6363.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/slct.201800673
Vancouver
Tornquist BL, Bueno G de P, Willig JCM, Oliveira IM de, Stefani HA, Rafique J, Saba S, Iglesias BA, Botteselle GV, Manarin F. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) [Internet]. ChemistrySelect. 2018 ; 3 6358-6363.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/slct.201800673
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
Fonte: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1055/s-0036-1589090
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
Fonte: ChemistrySelect. Unidade: FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1002/slct.201701197
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
Fonte: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1002/ajoc.201700154
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
Fonte: Chemistry Select. Unidades: IQ, FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1002/slct.201600319
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
Fonte: Zeitschrift fur Kristallographie. Unidade: FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1515/zkri-2015-1911
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
Fonte: Zeitschrift fur Kristallographie - Crystalline Materials. Unidade: FCF
Assuntos: DIFRAÇÃO POR RAIOS X, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1515/zkri-2016-1931
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
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1002/ejoc.201301421
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
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: 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: 27 set. 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 set. 27 ] 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 set. 27 ] Available from: https://doi.org/10.1002/ejoc.201300009
Artigo de periodico
Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids (2010)
Stefani, Hélio Alexandre ; Amaral, Monica Franco Zanini Junqueira; Reyes-Rangel, Gloria; Vargas-Caporali, Jorge; Juaristi, Eusebio
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: AMINOÁCIDOS, PALÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids. European Journal of Organic Chemistry, v. 2010, n. 33, p. 6393-6403, 2010Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201000852. Acesso em: 27 set. 2024.
APA
Stefani, H. A., Amaral, M. F. Z. J., Reyes-Rangel, G., Vargas-Caporali, J., & Juaristi, E. (2010). Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids. European Journal of Organic Chemistry, 2010( 33), 6393-6403. doi:10.1002/ejoc.201000852
NLM
Stefani HA, Amaral MFZJ, Reyes-Rangel G, Vargas-Caporali J, Juaristi E. Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 33): 6393-6403.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.201000852
Vancouver
Stefani HA, Amaral MFZJ, Reyes-Rangel G, Vargas-Caporali J, Juaristi E. Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 33): 6393-6403.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/ejoc.201000852
Artigo de periodico
'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts (2010)
Gueogjian, Kemilla; Singh, Fateh Veer; Pena, Jesus Marcelo; Amaral, Mônica F. Z. J; Stefani, Hélio Alexandre
Fonte: Synlett. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUEOGJIAN, Kemilla et al. 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett, n. 3, p. 427-432, 2010Tradução . . Acesso em: 27 set. 2024.
APA
Gueogjian, K., Singh, F. V., Pena, J. M., Amaral, M. F. Z. J., & Stefani, H. A. (2010). 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett, ( 3), 427-432.
NLM
Gueogjian K, Singh FV, Pena JM, Amaral MFZJ, Stefani HA. 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett. 2010 ;( 3): 427-432.[citado 2024 set. 27 ]
Vancouver
Gueogjian K, Singh FV, Pena JM, Amaral MFZJ, Stefani HA. 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett. 2010 ;( 3): 427-432.[citado 2024 set. 27 ]
Artigo de periodico
Enantioselective arylations catalyzed by carbohydrate-based chiral amino alcohols (2010)
Wouters, Ana Dionéia; Trossini, Gustavo Henrique Goulart ; Stefani, Hélio Alexandre ; Lüdtke, Diogo Seibert
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: ALDEÍDOS, CARBOIDRATOS, BORO, ZINCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WOUTERS, Ana Dionéia et al. Enantioselective arylations catalyzed by carbohydrate-based chiral amino alcohols. European Journal of Organic Chemistry, v. 2010, n. 12, p. 2351-2356, 2010Tradução . . Disponível em: http://www3.interscience.wiley.com/cgi-bin/fulltext/123314361/PDFSTART. Acesso em: 27 set. 2024.
APA
Wouters, A. D., Trossini, G. H. G., Stefani, H. A., & Lüdtke, D. S. (2010). Enantioselective arylations catalyzed by carbohydrate-based chiral amino alcohols. European Journal of Organic Chemistry, 2010( 12), 2351-2356. Recuperado de http://www3.interscience.wiley.com/cgi-bin/fulltext/123314361/PDFSTART
NLM
Wouters AD, Trossini GHG, Stefani HA, Lüdtke DS. Enantioselective arylations catalyzed by carbohydrate-based chiral amino alcohols [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 12): 2351-2356.[citado 2024 set. 27 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/123314361/PDFSTART
Vancouver
Wouters AD, Trossini GHG, Stefani HA, Lüdtke DS. Enantioselective arylations catalyzed by carbohydrate-based chiral amino alcohols [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 12): 2351-2356.[citado 2024 set. 27 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/123314361/PDFSTART

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