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Parte de monografia/livro
Síntese biocatalítica de amidas e amidasgraxas derivadas do s-mandelato de Etila e potenciais aplicações cosméticas (2023)
Lima, Rafaely Nascimento ; Porto, Andre Luiz Meleiro
Source: Princípios de quimica 2. Unidade: IQSC
Subjects: QUÍMICA VERDE, CATÁLISE
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ABNT
LIMA, Rafaely Nascimento e PORTO, Andre Luiz Meleiro. Síntese biocatalítica de amidas e amidasgraxas derivadas do s-mandelato de Etila e potenciais aplicações cosméticas. Princípios de quimica 2. Tradução . Ponta Grossa: Instituto de Química de São Carlos, Universidade de São Paulo, 2023. p. 58 . Disponível em: https://doi.org/10.22533/at.ed.779230501. Acesso em: 07 out. 2024.
APA
Lima, R. N., & Porto, A. L. M. (2023). Síntese biocatalítica de amidas e amidasgraxas derivadas do s-mandelato de Etila e potenciais aplicações cosméticas. In Princípios de quimica 2 (p. 58 ). Ponta Grossa: Instituto de Química de São Carlos, Universidade de São Paulo. doi:10.22533/at.ed.779230501
NLM
Lima RN, Porto ALM. Síntese biocatalítica de amidas e amidasgraxas derivadas do s-mandelato de Etila e potenciais aplicações cosméticas [Internet]. In: Princípios de quimica 2. Ponta Grossa: Instituto de Química de São Carlos, Universidade de São Paulo; 2023. p. 58 .[citado 2024 out. 07 ] Available from: https://doi.org/10.22533/at.ed.779230501
Vancouver
Lima RN, Porto ALM. Síntese biocatalítica de amidas e amidasgraxas derivadas do s-mandelato de Etila e potenciais aplicações cosméticas [Internet]. In: Princípios de quimica 2. Ponta Grossa: Instituto de Química de São Carlos, Universidade de São Paulo; 2023. p. 58 .[citado 2024 out. 07 ] Available from: https://doi.org/10.22533/at.ed.779230501
Artigo de periodico
Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties (2022)
Zanin, Lucas Lima ; Jimenez, David Esteban Quintero ; Birolli, Willian Garcia ; Venâncio, Tiago ; Valdes, Talita Alvarenga; Leitão, Andrei ; Porto, Andre Luiz Meleiro
Source: Current Bioactive Compounds. Unidades: IQSC, BIOENGENHARIA
Subjects: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS, BACTERICIDAS, NEOPLASIAS, CATÁLISE
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ABNT
ZANIN, Lucas Lima et al. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties. Current Bioactive Compounds, v. 18, n. 4, p. e191121198117, 2022Tradução . . Disponível em: https://doi.org/10.2174/1573407217666211119092038. Acesso em: 07 out. 2024.
APA
Zanin, L. L., Jimenez, D. E. Q., Birolli, W. G., Venâncio, T., Valdes, T. A., Leitão, A., & Porto, A. L. M. (2022). Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties. Current Bioactive Compounds, 18( 4), e191121198117. doi:10.2174/1573407217666211119092038
NLM
Zanin LL, Jimenez DEQ, Birolli WG, Venâncio T, Valdes TA, Leitão A, Porto ALM. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties [Internet]. Current Bioactive Compounds. 2022 ; 18( 4): e191121198117.[citado 2024 out. 07 ] Available from: https://doi.org/10.2174/1573407217666211119092038
Vancouver
Zanin LL, Jimenez DEQ, Birolli WG, Venâncio T, Valdes TA, Leitão A, Porto ALM. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties [Internet]. Current Bioactive Compounds. 2022 ; 18( 4): e191121198117.[citado 2024 out. 07 ] Available from: https://doi.org/10.2174/1573407217666211119092038
Trabalho de evento-resumo
Biossíntese de nanopartículas de ouro pela bactéria endofítica Bacillus sp. da flor de lavandin e aplicação em reações de Knoevenagel (2022)
Viana, Juliana Galan ; Calixto, Lucas A.; Luis, Maria F. F.; Moraes, Daniel Angeli de ; Varanda, Laudemir Carlos ; Jimenez, David Esteban Quintero ; Porto, Andre Luiz Meleiro
Source: Libro de resúmenes. Conference titles: Simposio Latinoamericano de Biocatálisis y Biotransformaciones - SiLaByB. Unidades: IQSC, EESC
Subjects: CATÁLISE, NANOPARTÍCULAS, OURO, BACTÉRIAS
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ABNT
VIANA, Juliana Galan et al. Biossíntese de nanopartículas de ouro pela bactéria endofítica Bacillus sp. da flor de lavandin e aplicação em reações de Knoevenagel. 2022, Anais.. Santiago: Instituto de Química de São Carlos, Universidade de São Paulo, 2022. Disponível em: https://ivsilabyb.usach.cl/es. Acesso em: 07 out. 2024.
APA
Viana, J. G., Calixto, L. A., Luis, M. F. F., Moraes, D. A. de, Varanda, L. C., Jimenez, D. E. Q., & Porto, A. L. M. (2022). Biossíntese de nanopartículas de ouro pela bactéria endofítica Bacillus sp. da flor de lavandin e aplicação em reações de Knoevenagel. In Libro de resúmenes. Santiago: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://ivsilabyb.usach.cl/es
NLM
Viana JG, Calixto LA, Luis MFF, Moraes DA de, Varanda LC, Jimenez DEQ, Porto ALM. Biossíntese de nanopartículas de ouro pela bactéria endofítica Bacillus sp. da flor de lavandin e aplicação em reações de Knoevenagel [Internet]. Libro de resúmenes. 2022 ;[citado 2024 out. 07 ] Available from: https://ivsilabyb.usach.cl/es
Vancouver
Viana JG, Calixto LA, Luis MFF, Moraes DA de, Varanda LC, Jimenez DEQ, Porto ALM. Biossíntese de nanopartículas de ouro pela bactéria endofítica Bacillus sp. da flor de lavandin e aplicação em reações de Knoevenagel [Internet]. Libro de resúmenes. 2022 ;[citado 2024 out. 07 ] Available from: https://ivsilabyb.usach.cl/es
Parte de monografia/livro
Promiscuous Activity of Hydrolases (2021)
Orozco, Erika Vanessa Meñaca ; Porto, Andre Luiz Meleiro
Source: Biocatalysis for Practitioners: Techniques, Reactions and Applications. Unidades: IQSC, IQ
Subjects: CATÁLISE, ENZIMAS HIDROLÍTICAS
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ABNT
OROZCO, Erika Vanessa Meñaca e PORTO, Andre Luiz Meleiro. Promiscuous Activity of Hydrolases. Biocatalysis for Practitioners: Techniques, Reactions and Applications. Tradução . Weinheim: Instituto de Química de São Carlos, Universidade de São Paulo, 2021. p. 528 . Disponível em: https://doi.org/10.1002/9783527824465.ch5. Acesso em: 07 out. 2024.
APA
Orozco, E. V. M., & Porto, A. L. M. (2021). Promiscuous Activity of Hydrolases. In Biocatalysis for Practitioners: Techniques, Reactions and Applications (p. 528 ). Weinheim: Instituto de Química de São Carlos, Universidade de São Paulo. doi:10.1002/9783527824465.ch5
NLM
Orozco EVM, Porto ALM. Promiscuous Activity of Hydrolases [Internet]. In: Biocatalysis for Practitioners: Techniques, Reactions and Applications. Weinheim: Instituto de Química de São Carlos, Universidade de São Paulo; 2021. p. 528 .[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/9783527824465.ch5
Vancouver
Orozco EVM, Porto ALM. Promiscuous Activity of Hydrolases [Internet]. In: Biocatalysis for Practitioners: Techniques, Reactions and Applications. Weinheim: Instituto de Química de São Carlos, Universidade de São Paulo; 2021. p. 528 .[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/9783527824465.ch5
Artigo de periodico
High-throughput screening for distinguishing nitrilases from nitrile hydratases in Aspergillus and application of a Box–Behnken design for the optimization of nitrilase (2021)
Santos, Edvan do Carmo; Menezes, Luiz Henrique Sales de; Santos, Carolline Silva; Santana, Paulo Vinicius Bispo; Soares, Glêydison Amarante ; Tavares, Iasnaia Maria de Carvalho ; Freitas, Janaina de Silva; Souza-Motta, Cristina Maria; Bezerra, José Luiz; Costa, Andréa Miura da ; Uetanabaro, Ana Paula Trovatti ; Porto, Andre Luiz Meleiro ; Franco, Marcelo; Oliveira, Julieta Rangel de
Source: Biotechnology and Applied Biochemistry. Unidade: IQSC
Subjects: CATÁLISE, HIDRÓLISE, NITRILAS, ASPERGILLUS
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ABNT
SANTOS, Edvan do Carmo et al. High-throughput screening for distinguishing nitrilases from nitrile hydratases in Aspergillus and application of a Box–Behnken design for the optimization of nitrilase. Biotechnology and Applied Biochemistry, p. 1- 10, 2021Tradução . . Disponível em: https://doi.org/10.1002/bab.2269. Acesso em: 07 out. 2024.
APA
Santos, E. do C., Menezes, L. H. S. de, Santos, C. S., Santana, P. V. B., Soares, G. A., Tavares, I. M. de C., et al. (2021). High-throughput screening for distinguishing nitrilases from nitrile hydratases in Aspergillus and application of a Box–Behnken design for the optimization of nitrilase. Biotechnology and Applied Biochemistry, 1- 10. doi:10.1002/bab.2269
NLM
Santos E do C, Menezes LHS de, Santos CS, Santana PVB, Soares GA, Tavares IM de C, Freitas J de S, Souza-Motta CM, Bezerra JL, Costa AM da, Uetanabaro APT, Porto ALM, Franco M, Oliveira JR de. High-throughput screening for distinguishing nitrilases from nitrile hydratases in Aspergillus and application of a Box–Behnken design for the optimization of nitrilase [Internet]. Biotechnology and Applied Biochemistry. 2021 ; 1- 10.[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/bab.2269
Vancouver
Santos E do C, Menezes LHS de, Santos CS, Santana PVB, Soares GA, Tavares IM de C, Freitas J de S, Souza-Motta CM, Bezerra JL, Costa AM da, Uetanabaro APT, Porto ALM, Franco M, Oliveira JR de. High-throughput screening for distinguishing nitrilases from nitrile hydratases in Aspergillus and application of a Box–Behnken design for the optimization of nitrilase [Internet]. Biotechnology and Applied Biochemistry. 2021 ; 1- 10.[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/bab.2269
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: 07 out. 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 out. 07 ] 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 out. 07 ] Available from: https://doi.org/10.1021/acscatal.9b04611
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
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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: 07 out. 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 out. 07 ] 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 out. 07 ] Available from: https://doi.org/10.1016/j.biortech.2019.122441
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: 07 out. 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 out. 07 ] 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 out. 07 ] 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: 07 out. 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 out. 07 ] 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 out. 07 ] Available from: https://doi.org/10.1007/s10126-020-09953-8
Artigo de periodico
Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra (2019)
Jimenez, David; Barreiro, Juliana Cristina; Santos Júnior, Fernando M. dos; Vasconcellos, Suzan; Vasconcellos, Suzan P de; Porto, Andre Luiz Meleiro ; Batista Junior, Fernando M
Source: Chirality. Unidade: IQSC
Assunto: CATÁLISE
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ABNT
JIMENEZ, David et al. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, v. 31, p. 534-542, 2019Tradução . . Disponível em: https://doi.org/10.1002/chir.23078. Acesso em: 07 out. 2024.
APA
Jimenez, D., Barreiro, J. C., Santos Júnior, F. M. dos, Vasconcellos, S., Vasconcellos, S. P. de, Porto, A. L. M., & Batista Junior, F. M. (2019). Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, 31, 534-542. doi:10.1002/chir.23078
NLM
Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/chir.23078
Vancouver
Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/chir.23078
Artigo de periodico
Amazon Oils from Andiroba (Carapa sp.) and Babassu (Orbignya sp.) for Preparation Biodiesel by Enzymatic Catalysis (2018)
Ferreira, Adriana Martini; Sena, Iracirema da S.; Magalhães, Keurison F; Oliveira, Samuel L; Ferreira, Iron M; Porto, Andre Luiz Meleiro
Source: Current biotechnology. Unidade: IQSC
Subjects: BIODIESEL, CATÁLISE, BABAÇU
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ABNT
FERREIRA, Adriana Martini et al. Amazon Oils from Andiroba (Carapa sp.) and Babassu (Orbignya sp.) for Preparation Biodiesel by Enzymatic Catalysis. Current biotechnology, v. 7, p. 428-437, 2018Tradução . . Disponível em: https://doi.org/10.2174/2211550108666190125115515. Acesso em: 07 out. 2024.
APA
Ferreira, A. M., Sena, I. da S., Magalhães, K. F., Oliveira, S. L., Ferreira, I. M., & Porto, A. L. M. (2018). Amazon Oils from Andiroba (Carapa sp.) and Babassu (Orbignya sp.) for Preparation Biodiesel by Enzymatic Catalysis. Current biotechnology, 7, 428-437. doi:10.2174/2211550108666190125115515
NLM
Ferreira AM, Sena I da S, Magalhães KF, Oliveira SL, Ferreira IM, Porto ALM. Amazon Oils from Andiroba (Carapa sp.) and Babassu (Orbignya sp.) for Preparation Biodiesel by Enzymatic Catalysis [Internet]. Current biotechnology. 2018 ;7 428-437.[citado 2024 out. 07 ] Available from: https://doi.org/10.2174/2211550108666190125115515
Vancouver
Ferreira AM, Sena I da S, Magalhães KF, Oliveira SL, Ferreira IM, Porto ALM. Amazon Oils from Andiroba (Carapa sp.) and Babassu (Orbignya sp.) for Preparation Biodiesel by Enzymatic Catalysis [Internet]. Current biotechnology. 2018 ;7 428-437.[citado 2024 out. 07 ] Available from: https://doi.org/10.2174/2211550108666190125115515
Artigo de periodico
Stereoselective reduction of 2-azido-1-phenylethanone derivatives by whole cells of marine-derived fungi applied to synthesisof enantioenriched β-hydroxy-1,2,3-triazoles (2017)
Alvarenga, Natália; Porto, Andre Luiz Meleiro
Source: Biocatalysis and Biotransformation. Unidade: IQSC
Subjects: MICRORGANISMOS CELULOLÍTICOS, CATÁLISE
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ABNT
ALVARENGA, Natália e PORTO, Andre Luiz Meleiro. Stereoselective reduction of 2-azido-1-phenylethanone derivatives by whole cells of marine-derived fungi applied to synthesisof enantioenriched β-hydroxy-1,2,3-triazoles. Biocatalysis and Biotransformation, v. 35, n. 6, p. 388-396, 2017Tradução . . Disponível em: https://doi.org/10.1080/10242422.2017.1352585. Acesso em: 07 out. 2024.
APA
Alvarenga, N., & Porto, A. L. M. (2017). Stereoselective reduction of 2-azido-1-phenylethanone derivatives by whole cells of marine-derived fungi applied to synthesisof enantioenriched β-hydroxy-1,2,3-triazoles. Biocatalysis and Biotransformation, 35( 6), 388-396. doi:10.1080/10242422.2017.1352585
NLM
Alvarenga N, Porto ALM. Stereoselective reduction of 2-azido-1-phenylethanone derivatives by whole cells of marine-derived fungi applied to synthesisof enantioenriched β-hydroxy-1,2,3-triazoles [Internet]. Biocatalysis and Biotransformation. 2017 ; 35( 6): 388-396.[citado 2024 out. 07 ] Available from: https://doi.org/10.1080/10242422.2017.1352585
Vancouver
Alvarenga N, Porto ALM. Stereoselective reduction of 2-azido-1-phenylethanone derivatives by whole cells of marine-derived fungi applied to synthesisof enantioenriched β-hydroxy-1,2,3-triazoles [Internet]. Biocatalysis and Biotransformation. 2017 ; 35( 6): 388-396.[citado 2024 out. 07 ] Available from: https://doi.org/10.1080/10242422.2017.1352585
Artigo de periodico
Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins (2017)
Ferreira , Irlon Maciel; Yoshioka, Sergio Akinobu ; Comasseto, João Valdir; Porto, Andre Luiz Meleiro
Source: RSC Advances. Unidades: IQSC, IQ
Subjects: ENZIMAS, CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA , Irlon Maciel et al. Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins. RSC Advances, v. 7, p. 12650-12658, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7ra00083a. Acesso em: 07 out. 2024.
APA
Ferreira , I. M., Yoshioka, S. A., Comasseto, J. V., & Porto, A. L. M. (2017). Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins. RSC Advances, 7, 12650-12658. doi:10.1039/c7ra00083a
NLM
Ferreira IM, Yoshioka SA, Comasseto JV, Porto ALM. Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins [Internet]. RSC Advances. 2017 ; 7 12650-12658.[citado 2024 out. 07 ] Available from: https://doi.org/10.1039/c7ra00083a
Vancouver
Ferreira IM, Yoshioka SA, Comasseto JV, Porto ALM. Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins [Internet]. RSC Advances. 2017 ; 7 12650-12658.[citado 2024 out. 07 ] Available from: https://doi.org/10.1039/c7ra00083a
Artigo de periodico
Alternative route for the synthesis of high surface-area h-Al2O3/Nb2O5 catalyst from aluminum waste (2016)
Nogueira, Francisco Guilherme Esteves; Asencios, Yvan Jesús Olortiga; Rodella, Cristiane B.; Porto, Andre Luiz Meleiro ; Assaf, Elisabete Moreira
Source: Materials Chemistry and Physics. Unidade: IQSC
Assunto: CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOGUEIRA, Francisco Guilherme Esteves et al. Alternative route for the synthesis of high surface-area h-Al2O3/Nb2O5 catalyst from aluminum waste. Materials Chemistry and Physics, v. 184, p. 23-30, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.matchemphys.2016.08.032. Acesso em: 07 out. 2024.
APA
Nogueira, F. G. E., Asencios, Y. J. O., Rodella, C. B., Porto, A. L. M., & Assaf, E. M. (2016). Alternative route for the synthesis of high surface-area h-Al2O3/Nb2O5 catalyst from aluminum waste. Materials Chemistry and Physics, 184, 23-30. doi:10.1016/j.matchemphys.2016.08.032
NLM
Nogueira FGE, Asencios YJO, Rodella CB, Porto ALM, Assaf EM. Alternative route for the synthesis of high surface-area h-Al2O3/Nb2O5 catalyst from aluminum waste [Internet]. Materials Chemistry and Physics. 2016 ; 184 23-30.[citado 2024 out. 07 ] Available from: https://doi.org/10.1016/j.matchemphys.2016.08.032
Vancouver
Nogueira FGE, Asencios YJO, Rodella CB, Porto ALM, Assaf EM. Alternative route for the synthesis of high surface-area h-Al2O3/Nb2O5 catalyst from aluminum waste [Internet]. Materials Chemistry and Physics. 2016 ; 184 23-30.[citado 2024 out. 07 ] Available from: https://doi.org/10.1016/j.matchemphys.2016.08.032

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