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Artigo de periodico
Versatile applications of cyanoacetic acid in organic chemistry: active methylene compound for the knoevenagel condensation and organocatalyst for the Biginelli reaction (2024)
Zanin, Lucas Lima ; Jimenez, David Esteban Quintero; Baia, Gabriel dos Santos; Marinho, Victor Hugo; Araújo, Inana Fauro de; Ramos, Ryan da Silva; Soto, Raimundo Nonato Picanço; Ferreira, Irlon Maciel; Santiago, Pedro Henrique de Oliveira ; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: Journal of the Brazilian Chemical Society. Unidades: IFSC, IQSC
Subjects: QUÍMICA VERDE, QUÍMICA ORGÂNICA
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ABNT
ZANIN, Lucas Lima et al. Versatile applications of cyanoacetic acid in organic chemistry: active methylene compound for the knoevenagel condensation and organocatalyst for the Biginelli reaction. Journal of the Brazilian Chemical Society, v. 35, n. 6, p. e-20240003-1-e-20240003-16, 2024Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20240003. Acesso em: 20 jun. 2024.
APA
Zanin, L. L., Jimenez, D. E. Q., Baia, G. dos S., Marinho, V. H., Araújo, I. F. de, Ramos, R. da S., et al. (2024). Versatile applications of cyanoacetic acid in organic chemistry: active methylene compound for the knoevenagel condensation and organocatalyst for the Biginelli reaction. Journal of the Brazilian Chemical Society, 35( 6), e-20240003-1-e-20240003-16. doi:10.21577/0103-5053.20240003
NLM
Zanin LL, Jimenez DEQ, Baia G dos S, Marinho VH, Araújo IF de, Ramos R da S, Soto RNP, Ferreira IM, Santiago PH de O, Ellena J, Porto ALM. Versatile applications of cyanoacetic acid in organic chemistry: active methylene compound for the knoevenagel condensation and organocatalyst for the Biginelli reaction [Internet]. Journal of the Brazilian Chemical Society. 2024 ; 35( 6): e-20240003-1-e-20240003-16.[citado 2024 jun. 20 ] Available from: https://doi.org/10.21577/0103-5053.20240003
Vancouver
Zanin LL, Jimenez DEQ, Baia G dos S, Marinho VH, Araújo IF de, Ramos R da S, Soto RNP, Ferreira IM, Santiago PH de O, Ellena J, Porto ALM. Versatile applications of cyanoacetic acid in organic chemistry: active methylene compound for the knoevenagel condensation and organocatalyst for the Biginelli reaction [Internet]. Journal of the Brazilian Chemical Society. 2024 ; 35( 6): e-20240003-1-e-20240003-16.[citado 2024 jun. 20 ] Available from: https://doi.org/10.21577/0103-5053.20240003
Artigo de periodico
Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation (2022)
Jimenez, David Esteban Quintero ; Zanin, Lucas Lima ; Ferreira, Irlon Maciel ; Deflon, Victor Marcelo ; Diniz, Luan F. ; Ellena, Javier ; Haiduke, Roberto Luiz Andrade ; Porto, Andre Luiz Meleiro
Source: Current Organic Chemistry. Unidades: IQSC, IFSC
Subjects: DIFRAÇÃO POR RAIOS X, FOTOQUÍMICA, QUÍMICA VERDE
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ABNT
JIMENEZ, David Esteban Quintero et al. Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation. Current Organic Chemistry, v. 26, n. 16, p. 1552-1564 + supplementary material, 2022Tradução . . Disponível em: https://doi.org/10.2174/1385272827666221125091631. Acesso em: 20 jun. 2024.
APA
Jimenez, D. E. Q., Zanin, L. L., Ferreira, I. M., Deflon, V. M., Diniz, L. F., Ellena, J., et al. (2022). Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation. Current Organic Chemistry, 26( 16), 1552-1564 + supplementary material. doi:10.2174/1385272827666221125091631
NLM
Jimenez DEQ, Zanin LL, Ferreira IM, Deflon VM, Diniz LF, Ellena J, Haiduke RLA, Porto ALM. Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation [Internet]. Current Organic Chemistry. 2022 ; 26( 16): 1552-1564 + supplementary material.[citado 2024 jun. 20 ] Available from: https://doi.org/10.2174/1385272827666221125091631
Vancouver
Jimenez DEQ, Zanin LL, Ferreira IM, Deflon VM, Diniz LF, Ellena J, Haiduke RLA, Porto ALM. Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation [Internet]. Current Organic Chemistry. 2022 ; 26( 16): 1552-1564 + supplementary material.[citado 2024 jun. 20 ] Available from: https://doi.org/10.2174/1385272827666221125091631
Artigo de periodico
Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre (2022)
Zanin, Lucas Lima ; Matos, Thiago Kelvin Brito ; Leitão, Andrei ; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: European Journal of Organic Chemistry. Unidades: IQSC, IFSC
Subjects: CINÉTICA, HIDRÓLISE
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ABNT
ZANIN, Lucas Lima et al. Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre. European Journal of Organic Chemistry, v. 2022, n. 38, p. e202200331-1-e202200331-8, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200331. Acesso em: 20 jun. 2024.
APA
Zanin, L. L., Matos, T. K. B., Leitão, A., Ellena, J., & Porto, A. L. M. (2022). Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre. European Journal of Organic Chemistry, 2022( 38), e202200331-1-e202200331-8. doi:10.1002/ejoc.202200331
NLM
Zanin LL, Matos TKB, Leitão A, Ellena J, Porto ALM. Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 38): e202200331-1-e202200331-8.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1002/ejoc.202200331
Vancouver
Zanin LL, Matos TKB, Leitão A, Ellena J, Porto ALM. Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 38): e202200331-1-e202200331-8.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1002/ejoc.202200331
Artigo de periodico
Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium (2021)
Zanin, Lucas Lima; Jimenez, David Esteban Quintero; Jesus, Matheus Pereira de ; Diniz, Luan Farinelli ; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: Journal of Molecular Structure. Unidades: IFSC, IQSC
Subjects: CRISTALOGRAFIA, DIFRAÇÃO POR RAIOS X, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANIN, Lucas Lima et al. Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium. Journal of Molecular Structure, v. 1223, n. Ja 2021, p. 129226-1-129226-10, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129226. Acesso em: 20 jun. 2024.
APA
Zanin, L. L., Jimenez, D. E. Q., Jesus, M. P. de, Diniz, L. F., Ellena, J., & Porto, A. L. M. (2021). Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium. Journal of Molecular Structure, 1223( Ja 2021), 129226-1-129226-10. doi:10.1016/j.molstruc.2020.129226
NLM
Zanin LL, Jimenez DEQ, Jesus MP de, Diniz LF, Ellena J, Porto ALM. Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium [Internet]. Journal of Molecular Structure. 2021 ; 1223( Ja 2021): 129226-1-129226-10.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129226
Vancouver
Zanin LL, Jimenez DEQ, Jesus MP de, Diniz LF, Ellena J, Porto ALM. Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium [Internet]. Journal of Molecular Structure. 2021 ; 1223( Ja 2021): 129226-1-129226-10.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129226
Artigo de periodico
Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 (2020)
Queiroz, Thayane Melo de; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: Marine Biotechnology. Unidades: IQSC, IFSC
Subjects: MEIO AMBIENTE, BIOTRANSFORMAÇÃO, FUNGOS, ESTEROIDES
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ABNT
QUEIROZ, Thayane Melo de e ELLENA, Javier e PORTO, Andre Luiz Meleiro. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996. Marine Biotechnology, v. 22, n. 5, p. 673-682, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10126-020-09989-w. Acesso em: 20 jun. 2024.
APA
Queiroz, T. M. de, Ellena, J., & Porto, A. L. M. (2020). Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996. Marine Biotechnology, 22( 5), 673-682. doi:10.1007/s10126-020-09989-w
NLM
Queiroz TM de, Ellena J, Porto ALM. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 [Internet]. Marine Biotechnology. 2020 ; 22( 5): 673-682.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1007/s10126-020-09989-w
Vancouver
Queiroz TM de, Ellena J, Porto ALM. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 [Internet]. Marine Biotechnology. 2020 ; 22( 5): 673-682.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1007/s10126-020-09989-w
Artigo de periodico
Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation (2019)
Jimenez, David Esteban Quintero; Zanin, Lucas Lima; Diniz, Luan Farinelli; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: Current Microwave Chemistry. Unidades: IFSC, IQSC
Subjects: TECNOLOGIA DE MICRO-ONDAS, CRISTALOGRAFIA ESTRUTURAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JIMENEZ, David Esteban Quintero et al. Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation. Current Microwave Chemistry, v. 6, n. 1, p. 54-60, 2019Tradução . . Disponível em: https://doi.org/10.2174/2213335606666190906123431. Acesso em: 20 jun. 2024.
APA
Jimenez, D. E. Q., Zanin, L. L., Diniz, L. F., Ellena, J., & Porto, A. L. M. (2019). Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation. Current Microwave Chemistry, 6( 1), 54-60. doi:10.2174/2213335606666190906123431
NLM
Jimenez DEQ, Zanin LL, Diniz LF, Ellena J, Porto ALM. Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation [Internet]. Current Microwave Chemistry. 2019 ; 6( 1): 54-60.[citado 2024 jun. 20 ] Available from: https://doi.org/10.2174/2213335606666190906123431
Vancouver
Jimenez DEQ, Zanin LL, Diniz LF, Ellena J, Porto ALM. Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation [Internet]. Current Microwave Chemistry. 2019 ; 6( 1): 54-60.[citado 2024 jun. 20 ] Available from: https://doi.org/10.2174/2213335606666190906123431

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