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Cellulose. Cellulose. Dordrecht: Instituto de Química, Universidade de São Paulo. Disponível em: https://link.springer.com/journal/10570/editors. Acesso em: 07 dez. 2025. , 2024
APA
Cellulose. (2024). Cellulose. Cellulose. Dordrecht: Instituto de Química, Universidade de São Paulo. Recuperado de https://link.springer.com/journal/10570/editors
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FROLLINI, Elisabete. Cellulose. Cellulose. Dordrecht: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://www.springer.com/journal/10570/editors. Acesso em: 07 dez. 2025. , 2023
APA
Frollini, E. (2023). Cellulose. Cellulose. Dordrecht: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://www.springer.com/journal/10570/editors
NLM
Frollini E. Cellulose [Internet]. Cellulose. 2023 ;[citado 2025 dez. 07 ] Available from: https://www.springer.com/journal/10570/editors
Vancouver
Frollini E. Cellulose [Internet]. Cellulose. 2023 ;[citado 2025 dez. 07 ] Available from: https://www.springer.com/journal/10570/editors
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Cellulose. Cellulose. Dordrecht: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://www.springer.com/journal/10570/editors. Acesso em: 07 dez. 2025. , 2022
APA
Cellulose. (2022). Cellulose. Cellulose. Dordrecht: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://www.springer.com/journal/10570/editors
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MELLO, Rodrigo Brito de e EMERY, Flavio da Silva. Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties. Journal of Fluorescence, v. 32, n. 1, p. 81-86, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10895-021-02831-z. Acesso em: 07 dez. 2025.
APA
Mello, R. B. de, & Emery, F. da S. (2021). Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties. Journal of Fluorescence, 32( 1), 81-86. doi:10.1007/s10895-021-02831-z
NLM
Mello RB de, Emery F da S. Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties [Internet]. Journal of Fluorescence. 2021 ; 32( 1): 81-86.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1007/s10895-021-02831-z
Vancouver
Mello RB de, Emery F da S. Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties [Internet]. Journal of Fluorescence. 2021 ; 32( 1): 81-86.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1007/s10895-021-02831-z
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CAIUBY, Clarice Alves Dale e JESUS, Matheus Pereira de e BURTOLOSO, Antonio Carlos Bender. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, v. 85, n. 11, p. 7433-7445 April 28, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.0c00833. Acesso em: 07 dez. 2025.
APA
Caiuby, C. A. D., Jesus, M. P. de, & Burtoloso, A. C. B. (2020). α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, 85( 11), 7433-7445 April 28. doi:10.1021/acs.joc.0c00833
NLM
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
Vancouver
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
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ALVES, Jacqueline Q. et al. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman. Journal of Coordination Chemistry, v. 73, n. 2, p. 191-205, 2020Tradução . . Disponível em: https://doi.org/10.1080/00958972.2020.1724287. Acesso em: 07 dez. 2025.
APA
Alves, J. Q., Formiga, A. L. B., Gonçalves, R. R., & Silva, R. S. da. (2020). Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman. Journal of Coordination Chemistry, 73( 2), 191-205. doi:10.1080/00958972.2020.1724287
NLM
Alves JQ, Formiga ALB, Gonçalves RR, Silva RS da. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman [Internet]. Journal of Coordination Chemistry. 2020 ; 73( 2): 191-205.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1080/00958972.2020.1724287
Vancouver
Alves JQ, Formiga ALB, Gonçalves RR, Silva RS da. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman [Internet]. Journal of Coordination Chemistry. 2020 ; 73( 2): 191-205.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1080/00958972.2020.1724287
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BERNARDIM, Barbara et al. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, v. 14, n. Ja 2019, p. 86-99, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41596-018-0083-9. Acesso em: 07 dez. 2025.
APA
Bernardim, B., Matos, M. J., Ferhati, X., Compañón, I., Guerreiro, A., Akkapeddi, P., et al. (2019). Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, 14( Ja 2019), 86-99. doi:10.1038/s41596-018-0083-9
NLM
Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
Vancouver
Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
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Cellulose. . Dordrecht: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/1dacbe9c-3810-4aca-815a-aa1449ca1451/P17909.pdf. Acesso em: 07 dez. 2025. , 2019
APA
Cellulose. (2019). Cellulose. Dordrecht: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/1dacbe9c-3810-4aca-815a-aa1449ca1451/P17909.pdf
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QUEIROZ, Thayane M et al. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, v. 5, n. 9, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2019.e02408. Acesso em: 07 dez. 2025.
APA
Queiroz, T. M., Orozco, E. V. M., Silva, V., Santos, L. S., Soares, M. B. P., Bezerra, D. P., & Porto, A. L. M. (2019). Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, 5( 9). doi:10.1016/j.heliyon.2019.e02408
NLM
Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2025 dez. 07 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
Vancouver
Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2025 dez. 07 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
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AHMAD, Anees e BURTOLOSO, Antonio Carlos Bender. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, v. 21, p. 6079-6083, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.9b02221. Acesso em: 07 dez. 2025.
APA
Ahmad, A., & Burtoloso, A. C. B. (2019). Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, 21, 6079-6083. doi:10.1021/acs.orglett.9b02221
NLM
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
Vancouver
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
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MELLO, Amanda C. et al. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones. The Journal of Organic Chemistry, v. 83, p. 11399-11406, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.8b01683. Acesso em: 07 dez. 2025.
APA
Mello, A. C., Momo, P. B., Burtoloso, A. C. B., & Amarante, G. W. (2018). Metal-free Insertion Reactions of Diazo carbonyls to Azlactones. The Journal of Organic Chemistry, 83, 11399-11406. doi:10.1021/acs.joc.8b01683
NLM
Mello AC, Momo PB, Burtoloso ACB, Amarante GW. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones [Internet]. The Journal of Organic Chemistry. 2018 ;83 11399-11406.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.joc.8b01683
Vancouver
Mello AC, Momo PB, Burtoloso ACB, Amarante GW. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones [Internet]. The Journal of Organic Chemistry. 2018 ;83 11399-11406.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.joc.8b01683
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MORAIS, Aline Teixeira do Brasil et al. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi. Biocatalysis and Agricultural Biotechnology, v. 16. p.314-319, 2018Tradução . . Disponível em: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd. Acesso em: 07 dez. 2025.
APA
Morais, A. T. do B., Ferreira , I. M., Jimenez, D. E. Q., & Porto, A. L. M. (2018). Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi. Biocatalysis and Agricultural Biotechnology, 16. p.314-319. doi:10.1016/j.bcab.2018.08.003
NLM
Morais AT do B, Ferreira IM, Jimenez DEQ, Porto ALM. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi [Internet]. Biocatalysis and Agricultural Biotechnology. 2018 ;16. p.314-319[citado 2025 dez. 07 ] Available from: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd
Vancouver
Morais AT do B, Ferreira IM, Jimenez DEQ, Porto ALM. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi [Internet]. Biocatalysis and Agricultural Biotechnology. 2018 ;16. p.314-319[citado 2025 dez. 07 ] Available from: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd
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ORENHA, Renato Pereira e TFOUNI, Elia e GALEMBECK, Sérgio Emanuel. How does the total charge and isomerism influence the Ru–NO ammine complexes?. Physical Chemistry Chemical Physics, v. 20, n. 19, p. 13348-13356, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8cp00865e. Acesso em: 07 dez. 2025.
APA
Orenha, R. P., Tfouni, E., & Galembeck, S. E. (2018). How does the total charge and isomerism influence the Ru–NO ammine complexes? Physical Chemistry Chemical Physics, 20( 19), 13348-13356. doi:10.1039/c8cp00865e
NLM
Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1039/c8cp00865e
Vancouver
Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1039/c8cp00865e
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GALLO, Rafael D. C e BURTOLOSO, Antonio Carlos Bender. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, v. 20, p. 4547-4556, 2018Tradução . . Disponível em: https://doi.org/10.1039/C8GC02574F. Acesso em: 07 dez. 2025.
APA
Gallo, R. D. C., & Burtoloso, A. C. B. (2018). Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, 20, 4547-4556. doi:10.1039/C8GC02574F
NLM
Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1039/C8GC02574F
Vancouver
Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1039/C8GC02574F
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TALERO, Alexánder G e MARTINS, Bruna S e BURTOLOSO, Antonio Carlos Bender. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones. Organic letters, v. 20, p. 7206-7211, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.8b03126. Acesso em: 07 dez. 2025.
APA
Talero, A. G., Martins, B. S., & Burtoloso, A. C. B. (2018). Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones. Organic letters, 20, 7206-7211. doi:10.1021/acs.orglett.8b03126
NLM
Talero AG, Martins BS, Burtoloso ACB. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones [Internet]. Organic letters. 2018 ;20 7206-7211.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.orglett.8b03126
Vancouver
Talero AG, Martins BS, Burtoloso ACB. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones [Internet]. Organic letters. 2018 ;20 7206-7211.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1021/acs.orglett.8b03126