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Artigo de periodico
Active copper species of co-precipitated copper-ceria catalysts in the CO-PROX reaction: an in situ XANES and DRIFTS study (2021)
Cruz, Aline Rodrigues Miranda; Assaf, Elisabete Moreira ; Gomes, Janaina Fernandes ; Assaf, Jose Mansur
Source: Catalysis Today. Unidade: IQSC
Subjects: CATÁLISE, OXIDAÇÃO, COBRE
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ABNT
CRUZ, Aline Rodrigues Miranda et al. Active copper species of co-precipitated copper-ceria catalysts in the CO-PROX reaction: an in situ XANES and DRIFTS study. Catalysis Today, v. 381, p. 42-49, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.cattod.2020.09.007. Acesso em: 08 ago. 2024.
APA
Cruz, A. R. M., Assaf, E. M., Gomes, J. F., & Assaf, J. M. (2021). Active copper species of co-precipitated copper-ceria catalysts in the CO-PROX reaction: an in situ XANES and DRIFTS study. Catalysis Today, 381, 42-49. doi:10.1016/j.cattod.2020.09.007
NLM
Cruz ARM, Assaf EM, Gomes JF, Assaf JM. Active copper species of co-precipitated copper-ceria catalysts in the CO-PROX reaction: an in situ XANES and DRIFTS study [Internet]. Catalysis Today. 2021 ; 381 42-49.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.cattod.2020.09.007
Vancouver
Cruz ARM, Assaf EM, Gomes JF, Assaf JM. Active copper species of co-precipitated copper-ceria catalysts in the CO-PROX reaction: an in situ XANES and DRIFTS study [Internet]. Catalysis Today. 2021 ; 381 42-49.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.cattod.2020.09.007
Artigo de periodico
Low-pressure hydrogenation of CO2 to methanol over Ni-Ga alloys synthesized by a surfactant-assisted co-precipitation method and a proposed mechanism by DRIFTS analysis (2021)
Rasteiro , Letícia Fernanda ; Rossi, Marco Aurélio de Lima Silva ; Assaf, Jose Mansur ; Assaf, Elisabete Moreira
Source: Catalysis Today. Unidade: IQSC
Subjects: CATÁLISE, METANOL
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RASTEIRO , Letícia Fernanda et al. Low-pressure hydrogenation of CO2 to methanol over Ni-Ga alloys synthesized by a surfactant-assisted co-precipitation method and a proposed mechanism by DRIFTS analysis. Catalysis Today, v. 381, p. 261-271, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.cattod.2020.05.067. Acesso em: 08 ago. 2024.
APA
Rasteiro , L. F., Rossi, M. A. de L. S., Assaf, J. M., & Assaf, E. M. (2021). Low-pressure hydrogenation of CO2 to methanol over Ni-Ga alloys synthesized by a surfactant-assisted co-precipitation method and a proposed mechanism by DRIFTS analysis. Catalysis Today, 381, 261-271. doi:10.1016/j.cattod.2020.05.067
NLM
Rasteiro LF, Rossi MA de LS, Assaf JM, Assaf EM. Low-pressure hydrogenation of CO2 to methanol over Ni-Ga alloys synthesized by a surfactant-assisted co-precipitation method and a proposed mechanism by DRIFTS analysis [Internet]. Catalysis Today. 2021 ; 381 261-271.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.cattod.2020.05.067
Vancouver
Rasteiro LF, Rossi MA de LS, Assaf JM, Assaf EM. Low-pressure hydrogenation of CO2 to methanol over Ni-Ga alloys synthesized by a surfactant-assisted co-precipitation method and a proposed mechanism by DRIFTS analysis [Internet]. Catalysis Today. 2021 ; 381 261-271.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.cattod.2020.05.067
Artigo de periodico
In situ-generated arene-ruthenium catalysts bearing cycloalkylamines for the ring-opening metathesis polymerization of norbornene (2021)
Oliveira, Douglas P; Cruz,Thais R; Martins, Daniele M; Maia, Pedro Ivo S; Machado, Antônio E. H. ; Bogado, André L; Goi, Beatriz E; Lima Neto, Benedito dos Santos ; Carvalho Jr, Valdemiro P
Source: Catalysis Today. Unidade: IQSC
Subjects: CATÁLISE, RUTÊNIO
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OLIVEIRA, Douglas P et al. In situ-generated arene-ruthenium catalysts bearing cycloalkylamines for the ring-opening metathesis polymerization of norbornene. Catalysis Today, v. 38, p. 34-41, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.cattod.2020.10.018. Acesso em: 08 ago. 2024.
APA
Oliveira, D. P., Cruz, T. R., Martins, D. M., Maia, P. I. S., Machado, A. E. H., Bogado, A. L., et al. (2021). In situ-generated arene-ruthenium catalysts bearing cycloalkylamines for the ring-opening metathesis polymerization of norbornene. Catalysis Today, 38, 34-41. doi:10.1016/j.cattod.2020.10.018
NLM
Oliveira DP, Cruz TR, Martins DM, Maia PIS, Machado AEH, Bogado AL, Goi BE, Lima Neto B dos S, Carvalho Jr VP. In situ-generated arene-ruthenium catalysts bearing cycloalkylamines for the ring-opening metathesis polymerization of norbornene [Internet]. Catalysis Today. 2021 ; 38 34-41.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.cattod.2020.10.018
Vancouver
Oliveira DP, Cruz TR, Martins DM, Maia PIS, Machado AEH, Bogado AL, Goi BE, Lima Neto B dos S, Carvalho Jr VP. In situ-generated arene-ruthenium catalysts bearing cycloalkylamines for the ring-opening metathesis polymerization of norbornene [Internet]. Catalysis Today. 2021 ; 38 34-41.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.cattod.2020.10.018
Artigo de periodico
Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids (2020)
Gallo, Rafael D. C; Momo, Patrícia B; Day, David P; Burtoloso, Antonio Carlos Bender
Source: Organic letters. Unidade: IQSC
Assunto: CATÁLISE
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GALLO, Rafael D. C et al. Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids. Organic letters, v. 22, n. 6, p. 2339-2343 March 5, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.0c00540. Acesso em: 08 ago. 2024.
APA
Gallo, R. D. C., Momo, P. B., Day, D. P., & Burtoloso, A. C. B. (2020). Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids. Organic letters, 22( 6), 2339-2343 March 5. doi:10.1021/acs.orglett.0c00540
NLM
Gallo RDC, Momo PB, Day DP, Burtoloso ACB. Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids [Internet]. Organic letters. 2020 ; 22( 6): 2339-2343 March 5.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acs.orglett.0c00540
Vancouver
Gallo RDC, Momo PB, Day DP, Burtoloso ACB. Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids [Internet]. Organic letters. 2020 ; 22( 6): 2339-2343 March 5.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acs.orglett.0c00540
Artigo de periodico
Adjusting Process Variables in Methane Tri-reforming to Achieve Suitable Syngas Quality and Low Coke Deposition (2020)
Lino, Ananda Vallezi Paladino ; Assaf, Elisabete Moreira ; Assaf, Jose Mansur
Source: Energy Fuels. Unidade: IQSC
Subjects: CATÁLISE, REATORES QUÍMICOS
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LINO, Ananda Vallezi Paladino e ASSAF, Elisabete Moreira e ASSAF, Jose Mansur. Adjusting Process Variables in Methane Tri-reforming to Achieve Suitable Syngas Quality and Low Coke Deposition. Energy Fuels, v. no2020, n. 12, p. 16522–16531, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.energyfuels.0c02895. Acesso em: 08 ago. 2024.
APA
Lino, A. V. P., Assaf, E. M., & Assaf, J. M. (2020). Adjusting Process Variables in Methane Tri-reforming to Achieve Suitable Syngas Quality and Low Coke Deposition. Energy Fuels, no2020( 12), 16522–16531. doi:10.1021/acs.energyfuels.0c02895
NLM
Lino AVP, Assaf EM, Assaf JM. Adjusting Process Variables in Methane Tri-reforming to Achieve Suitable Syngas Quality and Low Coke Deposition [Internet]. Energy Fuels. 2020 ; no2020( 12): 16522–16531.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acs.energyfuels.0c02895
Vancouver
Lino AVP, Assaf EM, Assaf JM. Adjusting Process Variables in Methane Tri-reforming to Achieve Suitable Syngas Quality and Low Coke Deposition [Internet]. Energy Fuels. 2020 ; no2020( 12): 16522–16531.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acs.energyfuels.0c02895
Artigo de periodico
Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation (2020)
Silva, Natália Alvarenga da ; Payer, Stefan E.; Petermeier, Philipp; Kohlfuerst, Christoph; Porto, Andre Luiz Meleiro ; Schrittwieser, Joerg H. ; Kroutil, Wolgang
Source: ACS Catalysis. Unidade: IQSC
Subjects: CATÁLISE, ALCALOIDES
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ABNT
SILVA, Natália Alvarenga da et al. Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation. ACS Catalysis, v. 10, n. 2, p. 1607-1620, 2020Tradução . . Disponível em: https://doi.org/10.1021/acscatal.9b04611. Acesso em: 08 ago. 2024.
APA
Silva, N. A. da, Payer, S. E., Petermeier, P., Kohlfuerst, C., Porto, A. L. M., Schrittwieser, J. H., & Kroutil, W. (2020). Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation. ACS Catalysis, 10( 2), 1607-1620. doi:10.1021/acscatal.9b04611
NLM
Silva NA da, Payer SE, Petermeier P, Kohlfuerst C, Porto ALM, Schrittwieser JH, Kroutil W. Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation [Internet]. ACS Catalysis. 2020 ; 10( 2): 1607-1620.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acscatal.9b04611
Vancouver
Silva NA da, Payer SE, Petermeier P, Kohlfuerst C, Porto ALM, Schrittwieser JH, Kroutil W. Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation [Internet]. ACS Catalysis. 2020 ; 10( 2): 1607-1620.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acscatal.9b04611
Artigo de periodico
Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities (2020)
Boldrini-França, Johara; Pinheiro-Júnior, Ernesto Lopes ; Peigneur, Steve; Pucca, Manuela Berto; Cerni, Felipe Augusto; Borges, Rafael Junqueira; Costa, Tássia Rafaella; Carone, Sante Emmanuel Imai; Fontes, Marcos Roberto de Mattos; Sampaio, Suely Vilela ; Arantes, Eliane Candiani ; Tytgat, Jan
Source: Scientific Reports. Unidade: FCFRP
Subjects: SEQUÊNCIA DE AMINOÁCIDOS, ANTINEOPLÁSICOS, FARMACOLOGIA, CATÁLISE, LINHAGEM CELULAR, CANAIS DE POTÁSSIO, ANTAGONISTAS, HEMOSTASIA, PROTEÍNAS RECOMBINANTES, VENENOS, PROTEÍNAS
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BOLDRINI-FRANÇA, Johara et al. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities. Scientific Reports, v. 10, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-61258-x. Acesso em: 08 ago. 2024.
APA
Boldrini-França, J., Pinheiro-Júnior, E. L., Peigneur, S., Pucca, M. B., Cerni, F. A., Borges, R. J., et al. (2020). Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities. Scientific Reports, 10( 1). doi:10.1038/s41598-020-61258-x
NLM
Boldrini-França J, Pinheiro-Júnior EL, Peigneur S, Pucca MB, Cerni FA, Borges RJ, Costa TR, Carone SEI, Fontes MR de M, Sampaio SV, Arantes EC, Tytgat J. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 ago. 08 ] Available from: https://doi.org/10.1038/s41598-020-61258-x
Vancouver
Boldrini-França J, Pinheiro-Júnior EL, Peigneur S, Pucca MB, Cerni FA, Borges RJ, Costa TR, Carone SEI, Fontes MR de M, Sampaio SV, Arantes EC, Tytgat J. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 ago. 08 ] Available from: https://doi.org/10.1038/s41598-020-61258-x
Artigo de periodico
Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides (2020)
Momo, Patrícia Betoni ; Leveille, Alexandria N. ; Farrar, Elliot H. E. ; Grayson, Matthew N. ; Mattson, Anita E.; Burtoloso, Antonio Carlos Bender
Source: Angewandte Chemie International Edition. Unidade: IQSC
Subjects: CATÁLISE, REAGENTES
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MOMO, Patrícia Betoni et al. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides. Angewandte Chemie International Edition, v. 59, p. 15554–15559 , 2020Tradução . . Disponível em: https://doi.org/10.1002/anie.202005563. Acesso em: 08 ago. 2024.
APA
Momo, P. B., Leveille, A. N., Farrar, E. H. E., Grayson, M. N., Mattson, A. E., & Burtoloso, A. C. B. (2020). Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides. Angewandte Chemie International Edition, 59, 15554–15559 . doi:10.1002/anie.202005563
NLM
Momo PB, Leveille AN, Farrar EHE, Grayson MN, Mattson AE, Burtoloso ACB. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides [Internet]. Angewandte Chemie International Edition. 2020 ; 59 15554–15559 .[citado 2024 ago. 08 ] Available from: https://doi.org/10.1002/anie.202005563
Vancouver
Momo PB, Leveille AN, Farrar EHE, Grayson MN, Mattson AE, Burtoloso ACB. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides [Internet]. Angewandte Chemie International Edition. 2020 ; 59 15554–15559 .[citado 2024 ago. 08 ] Available from: https://doi.org/10.1002/anie.202005563
Artigo de periodico
fac-[RuCl2(DMSO-S)3(n-butylamine)]: synthesis, structural characterization and dual catalytic performance (2020)
Silva, Tiago Breve da; Martins, Daniele Maria; Gois, Patrik D. S ; Borim, Patricia ; Maia, Pedro Ivo da Silva ; Carvalho Junior, Valdemiro Pereira de ; Lima Neto, Benedito dos Santos
Source: Inorganic Chemistry Communications. Unidade: IQSC
Subjects: CATÁLISE, RUTÊNIO
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SILVA, Tiago Breve da et al. fac-[RuCl2(DMSO-S)3(n-butylamine)]: synthesis, structural characterization and dual catalytic performance. Inorganic Chemistry Communications, v. 112, p. 107749, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.inoche.2019.107749. Acesso em: 08 ago. 2024.
APA
Silva, T. B. da, Martins, D. M., Gois, P. D. S., Borim, P., Maia, P. I. da S., Carvalho Junior, V. P. de, & Lima Neto, B. dos S. (2020). fac-[RuCl2(DMSO-S)3(n-butylamine)]: synthesis, structural characterization and dual catalytic performance. Inorganic Chemistry Communications, 112, 107749. doi:10.1016/j.inoche.2019.107749
NLM
Silva TB da, Martins DM, Gois PDS, Borim P, Maia PI da S, Carvalho Junior VP de, Lima Neto B dos S. fac-[RuCl2(DMSO-S)3(n-butylamine)]: synthesis, structural characterization and dual catalytic performance [Internet]. Inorganic Chemistry Communications. 2020 ; 112 107749.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.inoche.2019.107749
Vancouver
Silva TB da, Martins DM, Gois PDS, Borim P, Maia PI da S, Carvalho Junior VP de, Lima Neto B dos S. fac-[RuCl2(DMSO-S)3(n-butylamine)]: synthesis, structural characterization and dual catalytic performance [Internet]. Inorganic Chemistry Communications. 2020 ; 112 107749.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.inoche.2019.107749
Artigo de periodico
Group 10 metal complexes with a tetradentate thiosemicarbazonate ligand: Synthesis, crystal structures and computational insights into the catalysis for C–C coupling via Mizoroki-Heck reaction (2020)
Lima, Jackelinne C; Nascimento, Rebecca D.; Vilarinho, Luana M.; Borges, Alice P.; Silva, Leonardo H.F.; Souza, Jhonathan R.; Dinelli, Luis R.; Deflon, Victor Marcelo ; Machado, Antonio E. da Hora; Bogado, André L.; Maia, Pedro I.S.
Source: Journal of Molecular Structure. Unidade: IQSC
Assunto: CATÁLISE
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ABNT
LIMA, Jackelinne C et al. Group 10 metal complexes with a tetradentate thiosemicarbazonate ligand: Synthesis, crystal structures and computational insights into the catalysis for C–C coupling via Mizoroki-Heck reaction. Journal of Molecular Structure, v. 1199, p. 126997, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2019.126997. Acesso em: 08 ago. 2024.
APA
Lima, J. C., Nascimento, R. D., Vilarinho, L. M., Borges, A. P., Silva, L. H. F., Souza, J. R., et al. (2020). Group 10 metal complexes with a tetradentate thiosemicarbazonate ligand: Synthesis, crystal structures and computational insights into the catalysis for C–C coupling via Mizoroki-Heck reaction. Journal of Molecular Structure, 1199, 126997. doi:10.1016/j.molstruc.2019.126997
NLM
Lima JC, Nascimento RD, Vilarinho LM, Borges AP, Silva LHF, Souza JR, Dinelli LR, Deflon VM, Machado AE da H, Bogado AL, Maia PIS. Group 10 metal complexes with a tetradentate thiosemicarbazonate ligand: Synthesis, crystal structures and computational insights into the catalysis for C–C coupling via Mizoroki-Heck reaction [Internet]. Journal of Molecular Structure. 2020 ; 1199 126997.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.molstruc.2019.126997
Vancouver
Lima JC, Nascimento RD, Vilarinho LM, Borges AP, Silva LHF, Souza JR, Dinelli LR, Deflon VM, Machado AE da H, Bogado AL, Maia PIS. Group 10 metal complexes with a tetradentate thiosemicarbazonate ligand: Synthesis, crystal structures and computational insights into the catalysis for C–C coupling via Mizoroki-Heck reaction [Internet]. Journal of Molecular Structure. 2020 ; 1199 126997.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.molstruc.2019.126997
Artigo de periodico
A straightforward catalytic approach to obtain deuterated chloroform at room temperature (2020)
Higuera-Padilla, Angel Rubén ; Kock, Flávio Vinicius Crizóstomo ; Batista, Alzir Azevedo ; Colnago, Luiz Alberto
Source: Magnetic Resonance in Chemistry. Unidade: IQSC
Subjects: ESPECTROSCOPIA DE RESSONÂNCIA MAGNÉTICA NUCLEAR, CATÁLISE
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ABNT
HIGUERA-PADILLA, Angel Rubén et al. A straightforward catalytic approach to obtain deuterated chloroform at room temperature. Magnetic Resonance in Chemistry, v. 58, n. 10, p. 917-920, 2020Tradução . . Disponível em: https://doi.org/10.1002/mrc.5066. Acesso em: 08 ago. 2024.
APA
Higuera-Padilla, A. R., Kock, F. V. C., Batista, A. A., & Colnago, L. A. (2020). A straightforward catalytic approach to obtain deuterated chloroform at room temperature. Magnetic Resonance in Chemistry, 58( 10), 917-920. doi:10.1002/mrc.5066
NLM
Higuera-Padilla AR, Kock FVC, Batista AA, Colnago LA. A straightforward catalytic approach to obtain deuterated chloroform at room temperature [Internet]. Magnetic Resonance in Chemistry. 2020 ; 58( 10): 917-920.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1002/mrc.5066
Vancouver
Higuera-Padilla AR, Kock FVC, Batista AA, Colnago LA. A straightforward catalytic approach to obtain deuterated chloroform at room temperature [Internet]. Magnetic Resonance in Chemistry. 2020 ; 58( 10): 917-920.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1002/mrc.5066
Artigo de periodico
Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan (2020)
Ferreira, Irlon Maciel ; Fiamingo, Anderson; Campana Filho, Sergio Paulo ; Porto, Andre Luiz Meleiro
Source: Marine Biotechnology. Unidade: IQSC
Assunto: CATÁLISE
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ABNT
FERREIRA, Irlon Maciel et al. Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan. Marine Biotechnology, v. 22, p. 348-356, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10126-020-09954-7. Acesso em: 08 ago. 2024.
APA
Ferreira, I. M., Fiamingo, A., Campana Filho, S. P., & Porto, A. L. M. (2020). Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan. Marine Biotechnology, 22, 348-356. doi:10.1007%2Fs10126-020-09954-7
NLM
Ferreira IM, Fiamingo A, Campana Filho SP, Porto ALM. Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan [Internet]. Marine Biotechnology. 2020 ; 22 348-356.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1007/s10126-020-09954-7
Vancouver
Ferreira IM, Fiamingo A, Campana Filho SP, Porto ALM. Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan [Internet]. Marine Biotechnology. 2020 ; 22 348-356.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1007/s10126-020-09954-7
Artigo de periodico
Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives (2020)
Birolli, Willian Garcia ; Zanin, Lucas Lima; Jimenez, David Esteban Quintero; Porto, Andre Luiz Meleiro
Source: Marine Biotechnology. Unidade: IQSC
Assunto: CATÁLISE
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ABNT
BIROLLI, Willian Garcia et al. Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives. Marine Biotechnology, v. 22, p. 317–330, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10126-020-09953-8. Acesso em: 08 ago. 2024.
APA
Birolli, W. G., Zanin, L. L., Jimenez, D. E. Q., & Porto, A. L. M. (2020). Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives. Marine Biotechnology, 22, 317–330. doi:10.1007%2Fs10126-020-09953-8
NLM
Birolli WG, Zanin LL, Jimenez DEQ, Porto ALM. Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives [Internet]. Marine Biotechnology. 2020 ; 22 317–330.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1007/s10126-020-09953-8
Vancouver
Birolli WG, Zanin LL, Jimenez DEQ, Porto ALM. Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives [Internet]. Marine Biotechnology. 2020 ; 22 317–330.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1007/s10126-020-09953-8
Artigo de periodico
Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase (2020)
Birolli, Willian Garcia ; Porto, Andre Luiz Meleiro ; Fonseca, Luís Pina
Source: Bioresource Technology. Unidade: IQSC
Subjects: CATÁLISE, LIPASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BIROLLI, Willian Garcia e PORTO, Andre Luiz Meleiro e FONSECA, Luís Pina. Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase. Bioresource Technology, v. 297, p. 122441, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.biortech.2019.122441. Acesso em: 08 ago. 2024.
APA
Birolli, W. G., Porto, A. L. M., & Fonseca, L. P. (2020). Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase. Bioresource Technology, 297, 122441. doi:10.1016/j.biortech.2019.122441
NLM
Birolli WG, Porto ALM, Fonseca LP. Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase [Internet]. Bioresource Technology. 2020 ; 297 122441.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.biortech.2019.122441
Vancouver
Birolli WG, Porto ALM, Fonseca LP. Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase [Internet]. Bioresource Technology. 2020 ; 297 122441.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.biortech.2019.122441
Artigo de periodico
Adsorption of CO, NO, and H2 on the PdnAu55-n nanoclusters: DFT investigation within the van der Waals D3 corrections (2019)
Batista, Krys E. A; Silva, Juarez Lopes Ferreira da ; Piotrowski, Maurício J
Source: The Journal of Physical Chemistry C. Unidade: IQSC
Subjects: CATÁLISE, CATALISADORES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISTA, Krys E. A e SILVA, Juarez Lopes Ferreira da e PIOTROWSKI, Maurício J. Adsorption of CO, NO, and H2 on the PdnAu55-n nanoclusters: DFT investigation within the van der Waals D3 corrections. The Journal of Physical Chemistry C, v. 123, n. 12, p. 7431-7439, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.jpcc.8b12219. Acesso em: 08 ago. 2024.
APA
Batista, K. E. A., Silva, J. L. F. da, & Piotrowski, M. J. (2019). Adsorption of CO, NO, and H2 on the PdnAu55-n nanoclusters: DFT investigation within the van der Waals D3 corrections. The Journal of Physical Chemistry C, 123( 12), 7431-7439. doi:10.1021/acs.jpcc.8b12219
NLM
Batista KEA, Silva JLF da, Piotrowski MJ. Adsorption of CO, NO, and H2 on the PdnAu55-n nanoclusters: DFT investigation within the van der Waals D3 corrections [Internet]. The Journal of Physical Chemistry C. 2019 ;123( 12): 7431-7439.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acs.jpcc.8b12219
Vancouver
Batista KEA, Silva JLF da, Piotrowski MJ. Adsorption of CO, NO, and H2 on the PdnAu55-n nanoclusters: DFT investigation within the van der Waals D3 corrections [Internet]. The Journal of Physical Chemistry C. 2019 ;123( 12): 7431-7439.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acs.jpcc.8b12219
Artigo de periodico
Ruthenium-cymene containing pyridine-derived aldiimine ligands: Synthesis, characterization and application in the transfer hydrogenation of aryl ketones and kinetics studies (2019)
Ramos, Tiago S; Luz,Diego M.; Nascimento,Rebecca D.; Silva, Andressa K; Lião, luciano M; Miranda, Victor M; Deflon, Victor Marcelo ; Araujo, Márcio P. de; Ueno, Leonardo T; Machado, Francisco B. C; Dinelli, Luis R; Bogado, André L
Source: Journal of Organometallic Chemistry. Unidade: IQSC
Assunto: CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Tiago S et al. Ruthenium-cymene containing pyridine-derived aldiimine ligands: Synthesis, characterization and application in the transfer hydrogenation of aryl ketones and kinetics studies. Journal of Organometallic Chemistry, v. 892, p. 51-65, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2019.04.022. Acesso em: 08 ago. 2024.
APA
Ramos, T. S., Luz, D. M., Nascimento, R. D., Silva, A. K., Lião, luciano M., Miranda, V. M., et al. (2019). Ruthenium-cymene containing pyridine-derived aldiimine ligands: Synthesis, characterization and application in the transfer hydrogenation of aryl ketones and kinetics studies. Journal of Organometallic Chemistry, 892, 51-65. doi:10.1016/j.jorganchem.2019.04.022
NLM
Ramos TS, Luz DM, Nascimento RD, Silva AK, Lião luciano M, Miranda VM, Deflon VM, Araujo MP de, Ueno LT, Machado FBC, Dinelli LR, Bogado AL. Ruthenium-cymene containing pyridine-derived aldiimine ligands: Synthesis, characterization and application in the transfer hydrogenation of aryl ketones and kinetics studies [Internet]. Journal of Organometallic Chemistry. 2019 ; 892 51-65.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.04.022
Vancouver
Ramos TS, Luz DM, Nascimento RD, Silva AK, Lião luciano M, Miranda VM, Deflon VM, Araujo MP de, Ueno LT, Machado FBC, Dinelli LR, Bogado AL. Ruthenium-cymene containing pyridine-derived aldiimine ligands: Synthesis, characterization and application in the transfer hydrogenation of aryl ketones and kinetics studies [Internet]. Journal of Organometallic Chemistry. 2019 ; 892 51-65.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.04.022
Artigo de periodico
Synthesis, characterization and CO tolerance evaluation in PEMFCs of Pt2RuMo electrocatalysts (2019)
González-Hernández, Martin; Antolini, E; Perez, Joelma
Source: Catalysts. Unidade: IQSC
Subjects: ELETROCATÁLISE, CATÁLISE, CÉLULAS A COMBUSTÍVEL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GONZÁLEZ-HERNÁNDEZ, Martin e ANTOLINI, E e PEREZ, Joelma. Synthesis, characterization and CO tolerance evaluation in PEMFCs of Pt2RuMo electrocatalysts. Catalysts, v. 9, p. 61-73, 2019Tradução . . Disponível em: https://doi.org/10.3390/catal9010061. Acesso em: 08 ago. 2024.
APA
González-Hernández, M., Antolini, E., & Perez, J. (2019). Synthesis, characterization and CO tolerance evaluation in PEMFCs of Pt2RuMo electrocatalysts. Catalysts, 9, 61-73. doi:10.3390/catal9010061
NLM
González-Hernández M, Antolini E, Perez J. Synthesis, characterization and CO tolerance evaluation in PEMFCs of Pt2RuMo electrocatalysts [Internet]. Catalysts. 2019 ;9 61-73.[citado 2024 ago. 08 ] Available from: https://doi.org/10.3390/catal9010061
Vancouver
González-Hernández M, Antolini E, Perez J. Synthesis, characterization and CO tolerance evaluation in PEMFCs of Pt2RuMo electrocatalysts [Internet]. Catalysts. 2019 ;9 61-73.[citado 2024 ago. 08 ] Available from: https://doi.org/10.3390/catal9010061
Artigo de periodico
Structural vibrational and morphological properties of layered double hydroxides containing Ni2+, Zn2, Al3+ and Zr4+ cations (2017)
Bezerra, Débora M; Rodrigues, João Elias Figueiredo Soares; Assaf, Elisabete Moreira
Source: Materials Characterization. Unidade: IQSC
Assunto: CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BEZERRA, Débora M e RODRIGUES, João Elias Figueiredo Soares e ASSAF, Elisabete Moreira. Structural vibrational and morphological properties of layered double hydroxides containing Ni2+, Zn2, Al3+ and Zr4+ cations. Materials Characterization, v. 125, p. 29-36, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.matchar.2017.01.015. Acesso em: 08 ago. 2024.
APA
Bezerra, D. M., Rodrigues, J. E. F. S., & Assaf, E. M. (2017). Structural vibrational and morphological properties of layered double hydroxides containing Ni2+, Zn2, Al3+ and Zr4+ cations. Materials Characterization, 125, 29-36. doi:10.1016/j.matchar.2017.01.015
NLM
Bezerra DM, Rodrigues JEFS, Assaf EM. Structural vibrational and morphological properties of layered double hydroxides containing Ni2+, Zn2, Al3+ and Zr4+ cations [Internet]. Materials Characterization. 2017 ; 125 29-36.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.matchar.2017.01.015
Vancouver
Bezerra DM, Rodrigues JEFS, Assaf EM. Structural vibrational and morphological properties of layered double hydroxides containing Ni2+, Zn2, Al3+ and Zr4+ cations [Internet]. Materials Characterization. 2017 ; 125 29-36.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.matchar.2017.01.015
Artigo de periodico
Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides (2017)
Chiu, Megan; Metzker, Gustavo; Bernt, Christopher M; Tran, Anthony T.; Burtoloso, Antonio Carlos Bender ; Ford, Peter C
Source: ACS Sustainable Chemistry & Engineering. Unidade: IQSC
Assunto: CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHIU, Megan et al. Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides. ACS Sustainable Chemistry & Engineering, v. 5, n. 4, p. 3158–3169, 2017Tradução . . Disponível em: https://doi.org/10.1021/acssuschemeng.6b02954. Acesso em: 08 ago. 2024.
APA
Chiu, M., Metzker, G., Bernt, C. M., Tran, A. T., Burtoloso, A. C. B., & Ford, P. C. (2017). Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides. ACS Sustainable Chemistry & Engineering, 5( 4), 3158–3169. doi:10.1021/acssuschemeng.6b02954
NLM
Chiu M, Metzker G, Bernt CM, Tran AT, Burtoloso ACB, Ford PC. Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides [Internet]. ACS Sustainable Chemistry & Engineering. 2017 ; 5( 4): 3158–3169.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acssuschemeng.6b02954
Vancouver
Chiu M, Metzker G, Bernt CM, Tran AT, Burtoloso ACB, Ford PC. Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides [Internet]. ACS Sustainable Chemistry & Engineering. 2017 ; 5( 4): 3158–3169.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1021/acssuschemeng.6b02954
Artigo de periodico
Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application (2016)
Mouad, Ana Maria; Taupin, Delphine; Lehr, Laurent; Yvergnaux, Florent; Porto, Andre Luiz Meleiro
Source: Journal of Molecular Catalysis B: enzymatic. Unidade: IQSC
Assunto: CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOUAD, Ana Maria et al. Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application. Journal of Molecular Catalysis B: enzymatic, v. 126, p. 64-68, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2016.01.002. Acesso em: 08 ago. 2024.
APA
Mouad, A. M., Taupin, D., Lehr, L., Yvergnaux, F., & Porto, A. L. M. (2016). Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application. Journal of Molecular Catalysis B: enzymatic, 126, 64-68. doi:10.1016/j.molcatb.2016.01.002
NLM
Mouad AM, Taupin D, Lehr L, Yvergnaux F, Porto ALM. Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application [Internet]. Journal of Molecular Catalysis B: enzymatic. 2016 ; 126 64-68.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.molcatb.2016.01.002
Vancouver
Mouad AM, Taupin D, Lehr L, Yvergnaux F, Porto ALM. Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application [Internet]. Journal of Molecular Catalysis B: enzymatic. 2016 ; 126 64-68.[citado 2024 ago. 08 ] Available from: https://doi.org/10.1016/j.molcatb.2016.01.002

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