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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
Source: ChemCatChem. Unidades: FCF, IQ
Subjects: 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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://doi.org/10.1002/cctc.202000395
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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://doi.org/10.1039/c9ra00523d
Artigo de periodico
Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source (2019)
Darbem, Mariana P; Kanno, Karina S; Oliveira, Isadora M. de; Esteves, C. Henrique A; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: New Journal of Chemistry. Unidade: FCF
Subjects: MONÓXIDO DE CARBONO, MOLIBDÊNIO
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ABNT
DARBEM, Mariana P et al. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, v. 43, n. 2, p. 696-699, 2019Tradução . . Disponível em: https://doi.org/10.1039/c8nj04540b. Acesso em: 11 jun. 2024.
APA
Darbem, M. P., Kanno, K. S., Oliveira, I. M. de, Esteves, C. H. A., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, 43( 2), 696-699. doi:10.1039/c8nj04540b
NLM
Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1039/c8nj04540b
Vancouver
Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1039/c8nj04540b
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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://doi.org/10.1002/ajoc.201700154
Artigo de periodico
Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties (2016)
Barbeiro, Cristiane S; Vasconcelos, Stanley Nunes Siqueira; Schpector, Júlio Zukerman; Caracelli, Ignez; Pimenta, Daniel C; Rodrigues, Ana Clara Beltran; Fernandes, André S; Correra, Thiago Carita ; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Source: ChemistrySelect. Unidades: IQ, FCF
Subjects: MECANISMOS, FLUORESCÊNCIA
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ABNT
BARBEIRO, Cristiane S et al. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, v. 2, p. 5647–5652, 2016Tradução . . Disponível em: https://doi.org/10.1002/slct.201601526. Acesso em: 11 jun. 2024.
APA
Barbeiro, C. S., Vasconcelos, S. N. S., Schpector, J. Z., Caracelli, I., Pimenta, D. C., Rodrigues, A. C. B., et al. (2016). Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, 2, 5647–5652. doi:10.1002/slct.201601526
NLM
Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1002/slct.201601526
Vancouver
Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1002/slct.201601526

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