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Artigo de periodico
Ene-reductases: Contribution from Brazilian fungi in organic synthesis (2023)
Ferreira, Irlon Maciel ; Jimenez, David Esteban Quintero ; Lopes, Samuel Q.; Oliveira, Alex Nazaré de ; Matos, Mateus J S; Porto, Andre Luiz Meleiro
Source: Results in Chemistry. Unidade: IQSC
Subjects: BIOMA, SÍNTESE ORGÂNICA, FUNGOS, MEIO AMBIENTE
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ABNT
FERREIRA, Irlon Maciel et al. Ene-reductases: Contribution from Brazilian fungi in organic synthesis. Results in Chemistry, v. 5 , p. 100965, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.rechem.2023.100965. Acesso em: 02 out. 2024.
APA
Ferreira, I. M., Jimenez, D. E. Q., Lopes, S. Q., Oliveira, A. N. de, Matos, M. J. S., & Porto, A. L. M. (2023). Ene-reductases: Contribution from Brazilian fungi in organic synthesis. Results in Chemistry, 5 , 100965. doi:10.1016/j.rechem.2023.100965
NLM
Ferreira IM, Jimenez DEQ, Lopes SQ, Oliveira AN de, Matos MJS, Porto ALM. Ene-reductases: Contribution from Brazilian fungi in organic synthesis [Internet]. Results in Chemistry. 2023 ;5 100965.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.rechem.2023.100965
Vancouver
Ferreira IM, Jimenez DEQ, Lopes SQ, Oliveira AN de, Matos MJS, Porto ALM. Ene-reductases: Contribution from Brazilian fungi in organic synthesis [Internet]. Results in Chemistry. 2023 ;5 100965.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.rechem.2023.100965
Artigo de periodico
Polyurethane films formation from microcrystalline cellulose as a polyol and cellulose nanocrystals as additive: reactions favored by the low viscosity of the source of isocyanate groups used (2023)
Porto, Deyvid de Souza ; Faria, Clara Maria Gonçalves de ; Inada, Natalia Mayumi ; Frollini, Elisabete
Source: International Journal of Biological Macromolecules. Unidades: IFSC, IQSC
Subjects: FÍSICO-QUÍMICA, CELULOSE, NANOPARTÍCULAS, SÍNTESE ORGÂNICA
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ABNT
PORTO, Deyvid de Souza et al. Polyurethane films formation from microcrystalline cellulose as a polyol and cellulose nanocrystals as additive: reactions favored by the low viscosity of the source of isocyanate groups used. International Journal of Biological Macromolecules, v. 236, p. 124035-1-124035-14, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.124035. Acesso em: 02 out. 2024.
APA
Porto, D. de S., Faria, C. M. G. de, Inada, N. M., & Frollini, E. (2023). Polyurethane films formation from microcrystalline cellulose as a polyol and cellulose nanocrystals as additive: reactions favored by the low viscosity of the source of isocyanate groups used. International Journal of Biological Macromolecules, 236, 124035-1-124035-14. doi:10.1016/j.ijbiomac.2023.124035
NLM
Porto D de S, Faria CMG de, Inada NM, Frollini E. Polyurethane films formation from microcrystalline cellulose as a polyol and cellulose nanocrystals as additive: reactions favored by the low viscosity of the source of isocyanate groups used [Internet]. International Journal of Biological Macromolecules. 2023 ; 236 124035-1-124035-14.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.124035
Vancouver
Porto D de S, Faria CMG de, Inada NM, Frollini E. Polyurethane films formation from microcrystalline cellulose as a polyol and cellulose nanocrystals as additive: reactions favored by the low viscosity of the source of isocyanate groups used [Internet]. International Journal of Biological Macromolecules. 2023 ; 236 124035-1-124035-14.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.124035
Artigo de periodico
Biocatalytic synthesis of lipophilic amides by the lipase of Candida antarctica type B (2022)
Lima, Rafaely Nascimento ; Anjos, Charlene Souza dos ; Porto, Andre Luiz Meleiro
Source: Molecular Catalysis. Unidade: IQSC
Subjects: ESTERIFICAÇÃO, AMIDAS, SÍNTESE ORGÂNICA
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ABNT
LIMA, Rafaely Nascimento e ANJOS, Charlene Souza dos e PORTO, Andre Luiz Meleiro. Biocatalytic synthesis of lipophilic amides by the lipase of Candida antarctica type B. Molecular Catalysis, v. 530, p. 112635, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.mcat.2022.112635. Acesso em: 02 out. 2024.
APA
Lima, R. N., Anjos, C. S. dos, & Porto, A. L. M. (2022). Biocatalytic synthesis of lipophilic amides by the lipase of Candida antarctica type B. Molecular Catalysis, 530, 112635. doi:10.1016/j.mcat.2022.112635
NLM
Lima RN, Anjos CS dos, Porto ALM. Biocatalytic synthesis of lipophilic amides by the lipase of Candida antarctica type B [Internet]. Molecular Catalysis. 2022 ;530 112635.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.mcat.2022.112635
Vancouver
Lima RN, Anjos CS dos, Porto ALM. Biocatalytic synthesis of lipophilic amides by the lipase of Candida antarctica type B [Internet]. Molecular Catalysis. 2022 ;530 112635.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.mcat.2022.112635
Artigo de periodico
One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors (2022)
Lei, Yuting; Madalena, Ludmila dos Santos; Ossonon, Benjamin D.; Bimbi Junior, Fausto Eduardo; Chen, Jiyun; Lanza, Marcos Roberto de Vasconcelos ; Tavares, Ana C.
Source: Molecules: a journal of synthetic organic and natural product chemistry. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, ELETROQUÍMICA, REDUÇÃO
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ABNT
LEI, Yuting et al. One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors. Molecules: a journal of synthetic organic and natural product chemistry, v. 27, p. 7629, 2022Tradução . . Disponível em: https://doi.org/10.3390/molecules27217629. Acesso em: 02 out. 2024.
APA
Lei, Y., Madalena, L. dos S., Ossonon, B. D., Bimbi Junior, F. E., Chen, J., Lanza, M. R. de V., & Tavares, A. C. (2022). One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors. Molecules: a journal of synthetic organic and natural product chemistry, 27, 7629. doi:10.3390/molecules27217629
NLM
Lei Y, Madalena L dos S, Ossonon BD, Bimbi Junior FE, Chen J, Lanza MR de V, Tavares AC. One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors [Internet]. Molecules: a journal of synthetic organic and natural product chemistry. 2022 ;27 7629.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules27217629
Vancouver
Lei Y, Madalena L dos S, Ossonon BD, Bimbi Junior FE, Chen J, Lanza MR de V, Tavares AC. One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors [Internet]. Molecules: a journal of synthetic organic and natural product chemistry. 2022 ;27 7629.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules27217629
Artigo de periodico
Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network (2021)
Khalid, Muhammad ; Ali, Akbar ; Khan, Muhammad Usman ; Tahir, Muhammad Nawaz; Ahmad, Anees ; Ashfaq, Muhammad; Hussain, Riaz; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo
Source: Journal of Molecular Structure. Unidades: IQ, IQSC
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
KHALID, Muhammad et al. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, v. 1230 p. 129827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129827. Acesso em: 02 out. 2024.
APA
Khalid, M., Ali, A., Khan, M. U., Tahir, M. N., Ahmad, A., Ashfaq, M., et al. (2021). Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, 1230 p. 129827. doi:10.1016/j.molstruc.2020.129827
NLM
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Vancouver
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Artigo de periodico
Direct Synthesis of α‑Fluoro-α-Triazol-1-yl Ketones from Sulfoxonium Ylides:: A One-Pot Approach (2021)
Day, David Philip; Vargas, Jorge Andres Mora ; Burtoloso, Antonio Carlos Bender
Source: The Journal of Organic Chemistry. Unidade: IQSC
Subjects: CETONA, SÍNTESE ORGÂNICA
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ABNT
DAY, David Philip e VARGAS, Jorge Andres Mora e BURTOLOSO, Antonio Carlos Bender. Direct Synthesis of α‑Fluoro-α-Triazol-1-yl Ketones from Sulfoxonium Ylides:: A One-Pot Approach. The Journal of Organic Chemistry, v. 86, n. 17, p. 12427–12435, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.1c01441. Acesso em: 02 out. 2024.
APA
Day, D. P., Vargas, J. A. M., & Burtoloso, A. C. B. (2021). Direct Synthesis of α‑Fluoro-α-Triazol-1-yl Ketones from Sulfoxonium Ylides:: A One-Pot Approach. The Journal of Organic Chemistry, 86( 17), 12427–12435. doi:10.1021/acs.joc.1c01441
NLM
Day DP, Vargas JAM, Burtoloso ACB. Direct Synthesis of α‑Fluoro-α-Triazol-1-yl Ketones from Sulfoxonium Ylides:: A One-Pot Approach [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 17): 12427–12435.[citado 2024 out. 02 ] Available from: https://doi.org/10.1021/acs.joc.1c01441
Vancouver
Day DP, Vargas JAM, Burtoloso ACB. Direct Synthesis of α‑Fluoro-α-Triazol-1-yl Ketones from Sulfoxonium Ylides:: A One-Pot Approach [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 17): 12427–12435.[citado 2024 out. 02 ] Available from: https://doi.org/10.1021/acs.joc.1c01441
Artigo de periodico
Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling (2020)
Bernardim, Barbara ; Dunsmore, Lavinia ; Li, He; Hocking, Brad; Nuñez-Franco, Reyes; Navo, Claudio D. ; Jiménez-Osés, Gonzalo ; Burtoloso, Antonio Carlos Bender ; Bernardes, Gonçalo J. L.
Source: Bioconjugate Chemistry. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, REAGENTES, PROTEÍNAS, ANTICORPOS
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ABNT
BERNARDIM, Barbara et al. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling. Bioconjugate Chemistry, v. 31, n. 6, p. 1604-1610 June 2020, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.bioconjchem.0c00232. Acesso em: 02 out. 2024.
APA
Bernardim, B., Dunsmore, L., Li, H., Hocking, B., Nuñez-Franco, R., Navo, C. D., et al. (2020). Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling. Bioconjugate Chemistry, 31( 6), 1604-1610 June 2020. doi:10.1021/acs.bioconjchem.0c00232
NLM
Bernardim B, Dunsmore L, Li H, Hocking B, Nuñez-Franco R, Navo CD, Jiménez-Osés G, Burtoloso ACB, Bernardes GJL. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling [Internet]. Bioconjugate Chemistry. 2020 ; 31( 6): 1604-1610 June 2020.[citado 2024 out. 02 ] Available from: https://doi.org/10.1021/acs.bioconjchem.0c00232
Vancouver
Bernardim B, Dunsmore L, Li H, Hocking B, Nuñez-Franco R, Navo CD, Jiménez-Osés G, Burtoloso ACB, Bernardes GJL. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling [Internet]. Bioconjugate Chemistry. 2020 ; 31( 6): 1604-1610 June 2020.[citado 2024 out. 02 ] Available from: https://doi.org/10.1021/acs.bioconjchem.0c00232
Artigo de periodico
Syntheses and Applications of Malonamide Derivatives – A Minireview (2020)
Aderibigbe, Abiodun D.; Day, David P
Source: ChemistrySelect. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
ADERIBIGBE, Abiodun D. e DAY, David P. Syntheses and Applications of Malonamide Derivatives – A Minireview. ChemistrySelect, v. 5, p. 15222–15232, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202004340. Acesso em: 02 out. 2024.
APA
Aderibigbe, A. D., & Day, D. P. (2020). Syntheses and Applications of Malonamide Derivatives – A Minireview. ChemistrySelect, 5, 15222–15232. doi:10.1002/slct.202004340
NLM
Aderibigbe AD, Day DP. Syntheses and Applications of Malonamide Derivatives – A Minireview [Internet]. ChemistrySelect. 2020 ; 5 15222–15232.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/slct.202004340
Vancouver
Aderibigbe AD, Day DP. Syntheses and Applications of Malonamide Derivatives – A Minireview [Internet]. ChemistrySelect. 2020 ; 5 15222–15232.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/slct.202004340
Artigo de periodico
Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal (2016)
Kawamura, Meire Yasuko; Talero, Alexánder G; Santiago, João V; Garambel-Vilca, Edson; Rosset, Isac G; Burtoloso, Antonio Carlos Bender
Source: Journal of Organic Chemistry. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
KAWAMURA, Meire Yasuko et al. Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal. Journal of Organic Chemistry, v. 81, n. 21, p. 10569-10575, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b01575. Acesso em: 02 out. 2024.
APA
Kawamura, M. Y., Talero, A. G., Santiago, J. V., Garambel-Vilca, E., Rosset, I. G., & Burtoloso, A. C. B. (2016). Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal. Journal of Organic Chemistry, 81( 21), 10569-10575. doi:10.1021/acs.joc.6b01575
NLM
Kawamura MY, Talero AG, Santiago JV, Garambel-Vilca E, Rosset IG, Burtoloso ACB. Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal [Internet]. Journal of Organic Chemistry. 2016 ; 81( 21): 10569-10575.[citado 2024 out. 02 ] Available from: https://doi.org/10.1021/acs.joc.6b01575
Vancouver
Kawamura MY, Talero AG, Santiago JV, Garambel-Vilca E, Rosset IG, Burtoloso ACB. Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal [Internet]. Journal of Organic Chemistry. 2016 ; 81( 21): 10569-10575.[citado 2024 out. 02 ] Available from: https://doi.org/10.1021/acs.joc.6b01575
Artigo de periodico
Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds (2016)
Bernardim, Barbara; Couch, Erica D.; Hardman-Baldwin, Andrea M; Burtoloso, Antonio Carlos Bender ; Mattson, Anitta E
Source: Synthesis. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, UREIA
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ABNT
BERNARDIM, Barbara et al. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, v. 48, n. 5, p. 677-686, 2016Tradução . . Disponível em: https://doi.org/10.1055/s-0035-1561061. Acesso em: 02 out. 2024.
APA
Bernardim, B., Couch, E. D., Hardman-Baldwin, A. M., Burtoloso, A. C. B., & Mattson, A. E. (2016). Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, 48( 5), 677-686. doi:10.1055/s-0035-1561061
NLM
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2024 out. 02 ] Available from: https://doi.org/10.1055/s-0035-1561061
Vancouver
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2024 out. 02 ] Available from: https://doi.org/10.1055/s-0035-1561061

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