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Artigo de periodico
Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes (2023)
Baviera, Giovanni Stoppa; Donate, Paulo Marcos
Source: Synlett. Unidade: FFCLRP
Subjects: HIDROCARBONETOS POLICÍCLICOS, HIDROCARBONOS AROMÁTICOS, NIÓBIO, ÉTER
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ABNT
BAVIERA, Giovanni Stoppa e DONATE, Paulo Marcos. Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes. Synlett, v. 34, n. 16, p. 1915-1919, 2023Tradução . . Disponível em: https://doi.org/10.1055/s-0041-1738445. Acesso em: 05 dez. 2025.
APA
Baviera, G. S., & Donate, P. M. (2023). Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes. Synlett, 34( 16), 1915-1919. doi:10.1055/s-0041-1738445
NLM
Baviera GS, Donate PM. Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes [Internet]. Synlett. 2023 ; 34( 16): 1915-1919.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1055/s-0041-1738445
Vancouver
Baviera GS, Donate PM. Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes [Internet]. Synlett. 2023 ; 34( 16): 1915-1919.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1055/s-0041-1738445
Artigo de periodico
Hydrogenation of biomass-derived 5-hydroxymethylfurfural (HMF) over Pd catalysts in aqueous medium (2022)
Silva, Wesley Romário da; Rosolen, José Mauricio ; Donate, Paulo Marcos
Source: Orbital: The Electronic Journal of Chemistry. Unidade: FFCLRP
Subjects: HIDROGENAÇÃO, NANOTUBOS DE CARBONO, CARVÃO VEGETAL, PALÁDIO, COMPOSTOS ORGÂNICOS
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SILVA, Wesley Romário da e ROSOLEN, José Mauricio e DONATE, Paulo Marcos. Hydrogenation of biomass-derived 5-hydroxymethylfurfural (HMF) over Pd catalysts in aqueous medium. Orbital: The Electronic Journal of Chemistry, v. 14, n. 2, p. 74-81, 2022Tradução . . Disponível em: https://doi.org/10.17807/orbital.v14i2.15596. Acesso em: 05 dez. 2025.
APA
Silva, W. R. da, Rosolen, J. M., & Donate, P. M. (2022). Hydrogenation of biomass-derived 5-hydroxymethylfurfural (HMF) over Pd catalysts in aqueous medium. Orbital: The Electronic Journal of Chemistry, 14( 2), 74-81. doi:10.17807/orbital.v14i2.15596
NLM
Silva WR da, Rosolen JM, Donate PM. Hydrogenation of biomass-derived 5-hydroxymethylfurfural (HMF) over Pd catalysts in aqueous medium [Internet]. Orbital: The Electronic Journal of Chemistry. 2022 ; 14( 2): 74-81.[citado 2025 dez. 05 ] Available from: https://doi.org/10.17807/orbital.v14i2.15596
Vancouver
Silva WR da, Rosolen JM, Donate PM. Hydrogenation of biomass-derived 5-hydroxymethylfurfural (HMF) over Pd catalysts in aqueous medium [Internet]. Orbital: The Electronic Journal of Chemistry. 2022 ; 14( 2): 74-81.[citado 2025 dez. 05 ] Available from: https://doi.org/10.17807/orbital.v14i2.15596
Artigo de periodico
Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives (2021)
Donate, Paulo Marcos ; Barbosa, Hugo Elias
Source: Orbital: The Electronic Journal of Chemistry. Unidade: FFCLRP
Subjects: RADIAÇÃO ELETROMAGNÉTICA, TECNOLOGIA DE MICRO-ONDAS, SOLVENTE
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DONATE, Paulo Marcos e BARBOSA, Hugo Elias. Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives. Orbital: The Electronic Journal of Chemistry, v. 13, n. 4, p. 376-384, 2021Tradução . . Disponível em: https://doi.org/10.17807/orbital.v13i4.1657. Acesso em: 05 dez. 2025.
APA
Donate, P. M., & Barbosa, H. E. (2021). Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives. Orbital: The Electronic Journal of Chemistry, 13( 4), 376-384. doi:10.17807/orbital.v13i4.1657
NLM
Donate PM, Barbosa HE. Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives [Internet]. Orbital: The Electronic Journal of Chemistry. 2021 ; 13( 4): 376-384.[citado 2025 dez. 05 ] Available from: https://doi.org/10.17807/orbital.v13i4.1657
Vancouver
Donate PM, Barbosa HE. Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives [Internet]. Orbital: The Electronic Journal of Chemistry. 2021 ; 13( 4): 376-384.[citado 2025 dez. 05 ] Available from: https://doi.org/10.17807/orbital.v13i4.1657
Artigo de periodico
Pd catalysts supported on different hydrophilic or hydrophobic carbonaceous substrate for furfural and 5-(hydroxymethyl)-furfural hydrogenation in water (2021)
Silva, Wesley Romário da ; Matsubara, Elaine Yoshiko; Rosolen, José Mauricio ; Donate, Paulo Marcos ; Gunnella, Roberto
Source: Molecular Catalysis. Unidade: FFCLRP
Subjects: NANOPARTÍCULAS, PALÁDIO, NANOTUBOS, CARBONO, CARVÃO VEGETAL, HIDROGENAÇÃO, ÁGUA
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ABNT
SILVA, Wesley Romário da et al. Pd catalysts supported on different hydrophilic or hydrophobic carbonaceous substrate for furfural and 5-(hydroxymethyl)-furfural hydrogenation in water. Molecular Catalysis, v. 504, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.mcat.2021.111496. Acesso em: 05 dez. 2025.
APA
Silva, W. R. da, Matsubara, E. Y., Rosolen, J. M., Donate, P. M., & Gunnella, R. (2021). Pd catalysts supported on different hydrophilic or hydrophobic carbonaceous substrate for furfural and 5-(hydroxymethyl)-furfural hydrogenation in water. Molecular Catalysis, 504. doi:10.1016/j.mcat.2021.111496
NLM
Silva WR da, Matsubara EY, Rosolen JM, Donate PM, Gunnella R. Pd catalysts supported on different hydrophilic or hydrophobic carbonaceous substrate for furfural and 5-(hydroxymethyl)-furfural hydrogenation in water [Internet]. Molecular Catalysis. 2021 ; 504[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.mcat.2021.111496
Vancouver
Silva WR da, Matsubara EY, Rosolen JM, Donate PM, Gunnella R. Pd catalysts supported on different hydrophilic or hydrophobic carbonaceous substrate for furfural and 5-(hydroxymethyl)-furfural hydrogenation in water [Internet]. Molecular Catalysis. 2021 ; 504[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.mcat.2021.111496
Artigo de periodico
Recent advances in the syntheses of anthracene derivatives (2021)
Baviera, Giovanni Stoppa; Donate, Paulo Marcos
Source: Beilstein Journal of Organic Chemistry. Unidade: FFCLRP
Subjects: SÍNTESE QUÍMICA, POLÍMEROS (MATERIAIS), CÉLULAS SOLARES, HIDROCARBONETOS POLICÍCLICOS
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ABNT
BAVIERA, Giovanni Stoppa e DONATE, Paulo Marcos. Recent advances in the syntheses of anthracene derivatives. Beilstein Journal of Organic Chemistry, v. 17, p. 2028-2050, 2021Tradução . . Disponível em: https://doi.org/10.3762/bjoc.17.131. Acesso em: 05 dez. 2025.
APA
Baviera, G. S., & Donate, P. M. (2021). Recent advances in the syntheses of anthracene derivatives. Beilstein Journal of Organic Chemistry, 17, 2028-2050. doi:10.3762/bjoc.17.131
NLM
Baviera GS, Donate PM. Recent advances in the syntheses of anthracene derivatives [Internet]. Beilstein Journal of Organic Chemistry. 2021 ; 17 2028-2050.[citado 2025 dez. 05 ] Available from: https://doi.org/10.3762/bjoc.17.131
Vancouver
Baviera GS, Donate PM. Recent advances in the syntheses of anthracene derivatives [Internet]. Beilstein Journal of Organic Chemistry. 2021 ; 17 2028-2050.[citado 2025 dez. 05 ] Available from: https://doi.org/10.3762/bjoc.17.131
Artigo de periodico
Real-time monitoring of a cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction (2020)
Crotti, Antonio Eduardo Miller ; Previdi, Daniel; Donate, Paulo Marcos ; McIndoe, J. Scott
Source: Inorganica Chimica Acta. Unidade: FFCLRP
Subjects: ESPECTROMETRIA DE MASSAS, COBALTO, CATÁLISE
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ABNT
CROTTI, Antonio Eduardo Miller et al. Real-time monitoring of a cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction. Inorganica Chimica Acta, v. 508, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ica.2020.119654. Acesso em: 05 dez. 2025.
APA
Crotti, A. E. M., Previdi, D., Donate, P. M., & McIndoe, J. S. (2020). Real-time monitoring of a cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction. Inorganica Chimica Acta, 508. doi:10.1016/j.ica.2020.119654
NLM
Crotti AEM, Previdi D, Donate PM, McIndoe JS. Real-time monitoring of a cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction [Internet]. Inorganica Chimica Acta. 2020 ; 508[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.ica.2020.119654
Vancouver
Crotti AEM, Previdi D, Donate PM, McIndoe JS. Real-time monitoring of a cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction [Internet]. Inorganica Chimica Acta. 2020 ; 508[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.ica.2020.119654
Artigo de periodico
Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations (2019)
Previdi, Daniel ; Nardini, Viviani ; Celorio, Mayla Eduarda Rosa; Palaretti, Vinicius; Silva, Gil Valdo José da ; Donate, Paulo Marcos
Source: Journal of Molecular Structure. Unidades: FCFRP, FFCLRP
Subjects: ESTEREOQUÍMICA, RESSONÂNCIA MAGNÉTICA NUCLEAR, QUÍMICA MÉDICA
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ABNT
PREVIDI, Daniel et al. Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations. Journal of Molecular Structure, v. 1178, p. 467-478, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2018.10.064. Acesso em: 05 dez. 2025.
APA
Previdi, D., Nardini, V., Celorio, M. E. R., Palaretti, V., Silva, G. V. J. da, & Donate, P. M. (2019). Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations. Journal of Molecular Structure, 1178, 467-478. doi:10.1016/j.molstruc.2018.10.064
NLM
Previdi D, Nardini V, Celorio MER, Palaretti V, Silva GVJ da, Donate PM. Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations [Internet]. Journal of Molecular Structure. 2019 ;1178 467-478.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molstruc.2018.10.064
Vancouver
Previdi D, Nardini V, Celorio MER, Palaretti V, Silva GVJ da, Donate PM. Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations [Internet]. Journal of Molecular Structure. 2019 ;1178 467-478.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molstruc.2018.10.064
Artigo de periodico
Synthesis and antileishmanial activity of some functionalized peptoids (2019)
Previdi, Daniel; Rodrigues, Stephanie; Coelho, Mike Gustavo; Candido, Ana Carolina Bolela Bovo; Magalhães, Lizandra Guidi; Donate, Paulo Marcos
Source: Journal of the Brazilian Chemical Society. Unidade: FFCLRP
Subjects: QUÍMICA, PEPTÍDEOS, LEISHMANIA
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ABNT
PREVIDI, Daniel et al. Synthesis and antileishmanial activity of some functionalized peptoids. Journal of the Brazilian Chemical Society, v. 30, n. 6, p. 1334-1340, 2019Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20190023. Acesso em: 05 dez. 2025.
APA
Previdi, D., Rodrigues, S., Coelho, M. G., Candido, A. C. B. B., Magalhães, L. G., & Donate, P. M. (2019). Synthesis and antileishmanial activity of some functionalized peptoids. Journal of the Brazilian Chemical Society, 30( 6), 1334-1340. doi:10.21577/0103-5053.20190023
NLM
Previdi D, Rodrigues S, Coelho MG, Candido ACBB, Magalhães LG, Donate PM. Synthesis and antileishmanial activity of some functionalized peptoids [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 6): 1334-1340.[citado 2025 dez. 05 ] Available from: https://doi.org/10.21577/0103-5053.20190023
Vancouver
Previdi D, Rodrigues S, Coelho MG, Candido ACBB, Magalhães LG, Donate PM. Synthesis and antileishmanial activity of some functionalized peptoids [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 6): 1334-1340.[citado 2025 dez. 05 ] Available from: https://doi.org/10.21577/0103-5053.20190023
Artigo de periodico
Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes (2019)
Rodrigues, Shirley Muniz Machado; Previdi, Daniel; Baviera, Giovanni Stoppa; Matias, Alexandre A.; Donate, Paulo Marcos
Source: Synthesis. Unidade: FFCLRP
Subjects: COMPOSTOS ORGÂNICOS, NIÓBIO, ALDEÍDOS
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ABNT
RODRIGUES, Shirley Muniz Machado et al. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes. Synthesis, v. 51, n. 23, p. 4498-4506, 2019Tradução . . Disponível em: https://doi.org/10.1055/s-0037-1610727. Acesso em: 05 dez. 2025.
APA
Rodrigues, S. M. M., Previdi, D., Baviera, G. S., Matias, A. A., & Donate, P. M. (2019). Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes. Synthesis, 51( 23), 4498-4506. doi:10.1055/s-0037-1610727
NLM
Rodrigues SMM, Previdi D, Baviera GS, Matias AA, Donate PM. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes [Internet]. Synthesis. 2019 ; 51( 23): 4498-4506.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1055/s-0037-1610727
Vancouver
Rodrigues SMM, Previdi D, Baviera GS, Matias AA, Donate PM. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes [Internet]. Synthesis. 2019 ; 51( 23): 4498-4506.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1055/s-0037-1610727
Artigo de periodico
Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions (2018)
Ponte, Gino Del; Archanjo, Fernando C.; Watanabe, Lilian Y.; Donate, Paulo Marcos; Campos, Joaquín M.
Source: Arabian Journal of Chemistry. Unidades: FCFRP, FFCLRP
Subjects: SÍNTESE QUÍMICA, COMPOSTOS AROMÁTICOS, ANÉIS, ÍONS
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ABNT
PONTE, Gino Del et al. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions. Arabian Journal of Chemistry, v. 11, n. 3, p. 415-425, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.11.001. Acesso em: 05 dez. 2025.
APA
Ponte, G. D., Archanjo, F. C., Watanabe, L. Y., Donate, P. M., & Campos, J. M. (2018). Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions. Arabian Journal of Chemistry, 11( 3), 415-425. doi:10.1016/j.arabjc.2016.11.001
NLM
Ponte GD, Archanjo FC, Watanabe LY, Donate PM, Campos JM. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions [Internet]. Arabian Journal of Chemistry. 2018 ; 11( 3): 415-425.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.arabjc.2016.11.001
Vancouver
Ponte GD, Archanjo FC, Watanabe LY, Donate PM, Campos JM. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions [Internet]. Arabian Journal of Chemistry. 2018 ; 11( 3): 415-425.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.arabjc.2016.11.001
Artigo de periodico
The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells (2018)
Abd El-Salam, Mohamed ; Bastos, Jairo Kenupp; Han, Jing Jing; Previdi, Daniel ; Coelho, Eduardo Barbosa ; Donate, Paulo Marcos ; Romero, Michael F.; Lieske, John
Source: Journal of Medicinal Chemistry. Unidades: FCFRP, FMRP, FFCLRP
Subjects: FRAÇÕES SUBCELULARES, CÉLULAS, RIM, ANTIOXIDANTES, DROSOPHILA
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ABNT
ABD EL-SALAM, Mohamed et al. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells. Journal of Medicinal Chemistry, v. 61, n. 4, p. 1609-1621, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.7b01566. Acesso em: 05 dez. 2025.
APA
Abd El-Salam, M., Bastos, J. K., Han, J. J., Previdi, D., Coelho, E. B., Donate, P. M., et al. (2018). The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells. Journal of Medicinal Chemistry, 61( 4), 1609-1621. doi:10.1021/acs.jmedchem.7b01566
NLM
Abd El-Salam M, Bastos JK, Han JJ, Previdi D, Coelho EB, Donate PM, Romero MF, Lieske J. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 4): 1609-1621.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.jmedchem.7b01566
Vancouver
Abd El-Salam M, Bastos JK, Han JJ, Previdi D, Coelho EB, Donate PM, Romero MF, Lieske J. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 4): 1609-1621.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.jmedchem.7b01566
Artigo de periodico
Fast and efficient synthesis of maculalactone derivatives via the microwave technique (2017)
Previdi, Daniel; Rosa, Mayla E.; Donate, Paulo Marcos
Source: Current Microwave Chemistry. Unidade: FFCLRP
Subjects: SÍNTESE ORGÂNICA, PRODUTOS NATURAIS, CYANOPHYTA, RADIAÇÃO ELETROMAGNÉTICA
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ABNT
PREVIDI, Daniel e ROSA, Mayla E. e DONATE, Paulo Marcos. Fast and efficient synthesis of maculalactone derivatives via the microwave technique. Current Microwave Chemistry, v. 4, n. 3, p. 229-237, 2017Tradução . . Disponível em: https://doi.org/10.2174/2213335604666170616122835. Acesso em: 05 dez. 2025.
APA
Previdi, D., Rosa, M. E., & Donate, P. M. (2017). Fast and efficient synthesis of maculalactone derivatives via the microwave technique. Current Microwave Chemistry, 4( 3), 229-237. doi:10.2174/2213335604666170616122835
NLM
Previdi D, Rosa ME, Donate PM. Fast and efficient synthesis of maculalactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2017 ; 4( 3): 229-237.[citado 2025 dez. 05 ] Available from: https://doi.org/10.2174/2213335604666170616122835
Vancouver
Previdi D, Rosa ME, Donate PM. Fast and efficient synthesis of maculalactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2017 ; 4( 3): 229-237.[citado 2025 dez. 05 ] Available from: https://doi.org/10.2174/2213335604666170616122835
Artigo de periodico
Palladium decoration of hybrid carbon nanotubes/charcoal composite and its catalytic behavior in the hydrogenation of trans-cinnamaldehyde (2015)
Ribeiro, Pedro Henrique Zana; Matsubara, Elaine Y.; Rosolen, José Maurício; Donate, Paulo Marcos; Gunnella, Roberto
Source: Journal of Molecular Catalysis A: Chemical. Unidade: FFCLRP
Subjects: NANOPARTÍCULAS, PALÁDIO, HIDROGENAÇÃO
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ABNT
RIBEIRO, Pedro Henrique Zana et al. Palladium decoration of hybrid carbon nanotubes/charcoal composite and its catalytic behavior in the hydrogenation of trans-cinnamaldehyde. Journal of Molecular Catalysis A: Chemical, v. 410, p. 34-40, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.molcata.2015.08.027. Acesso em: 05 dez. 2025.
APA
Ribeiro, P. H. Z., Matsubara, E. Y., Rosolen, J. M., Donate, P. M., & Gunnella, R. (2015). Palladium decoration of hybrid carbon nanotubes/charcoal composite and its catalytic behavior in the hydrogenation of trans-cinnamaldehyde. Journal of Molecular Catalysis A: Chemical, 410, 34-40. doi:10.1016/j.molcata.2015.08.027
NLM
Ribeiro PHZ, Matsubara EY, Rosolen JM, Donate PM, Gunnella R. Palladium decoration of hybrid carbon nanotubes/charcoal composite and its catalytic behavior in the hydrogenation of trans-cinnamaldehyde [Internet]. Journal of Molecular Catalysis A: Chemical. 2015 ; 410 34-40.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molcata.2015.08.027
Vancouver
Ribeiro PHZ, Matsubara EY, Rosolen JM, Donate PM, Gunnella R. Palladium decoration of hybrid carbon nanotubes/charcoal composite and its catalytic behavior in the hydrogenation of trans-cinnamaldehyde [Internet]. Journal of Molecular Catalysis A: Chemical. 2015 ; 410 34-40.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molcata.2015.08.027
Artigo de periodico
Microwave-assisted green production of furfural from D-xylose of sugarcane bagasse (2015)
Vaz Junior, Sílvio; Donate, Paulo Marcos
Source: BioResources. Unidade: FFCLRP
Subjects: CANA-DE-AÇÚCAR, BAGAÇOS, ENZIMAS, TECNOLOGIA DE MICRO-ONDAS, QUÍMICA VERDE
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ABNT
VAZ JUNIOR, Sílvio e DONATE, Paulo Marcos. Microwave-assisted green production of furfural from D-xylose of sugarcane bagasse. BioResources, v. 10, n. 4, p. 8168-8180, 2015Tradução . . Disponível em: https://doi.org/10.15376/biores.10.4.8168-8180. Acesso em: 05 dez. 2025.
APA
Vaz Junior, S., & Donate, P. M. (2015). Microwave-assisted green production of furfural from D-xylose of sugarcane bagasse. BioResources, 10( 4), 8168-8180. doi:10.15376/biores.10.4.8168-8180
NLM
Vaz Junior S, Donate PM. Microwave-assisted green production of furfural from D-xylose of sugarcane bagasse [Internet]. BioResources. 2015 ; 10( 4): 8168-8180.[citado 2025 dez. 05 ] Available from: https://doi.org/10.15376/biores.10.4.8168-8180
Vancouver
Vaz Junior S, Donate PM. Microwave-assisted green production of furfural from D-xylose of sugarcane bagasse [Internet]. BioResources. 2015 ; 10( 4): 8168-8180.[citado 2025 dez. 05 ] Available from: https://doi.org/10.15376/biores.10.4.8168-8180
Artigo de periodico
A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique (2015)
Pinatto-Botelho, Marcos F; Donate, Paulo Marcos
Source: Current Microwave Chemistry. Unidade: FFCLRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, TECNOLOGIA DE MICRO-ONDAS, PRODUTOS NATURAIS
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ABNT
PINATTO-BOTELHO, Marcos F e DONATE, Paulo Marcos. A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique. Current Microwave Chemistry, v. 2, n. 1, p. 83-87, 2015Tradução . . Disponível em: https://doi.org/10.2174/221333560201150212113120. Acesso em: 05 dez. 2025.
APA
Pinatto-Botelho, M. F., & Donate, P. M. (2015). A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique. Current Microwave Chemistry, 2( 1), 83-87. doi:10.2174/221333560201150212113120
NLM
Pinatto-Botelho MF, Donate PM. A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2015 ; 2( 1): 83-87.[citado 2025 dez. 05 ] Available from: https://doi.org/10.2174/221333560201150212113120
Vancouver
Pinatto-Botelho MF, Donate PM. A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2015 ; 2( 1): 83-87.[citado 2025 dez. 05 ] Available from: https://doi.org/10.2174/221333560201150212113120
Artigo de periodico
New approach to the synthesis of the natural product aripuanin (2015)
Lazaro, Aline S; Ribeiro, Pedro H. Zana; Sairre, Mirela I; Donate, Paulo Marcos
Source: Synthetic Communications. Unidade: FFCLRP
Subjects: PRODUTOS NATURAIS (SÍNTESE QUÍMICA), SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAZARO, Aline S et al. New approach to the synthesis of the natural product aripuanin. Synthetic Communications, v. 45, n. 11, p. 1374-1378, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1021426. Acesso em: 05 dez. 2025.
APA
Lazaro, A. S., Ribeiro, P. H. Z., Sairre, M. I., & Donate, P. M. (2015). New approach to the synthesis of the natural product aripuanin. Synthetic Communications, 45( 11), 1374-1378. doi:10.1080/00397911.2015.1021426
NLM
Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1080/00397911.2015.1021426
Vancouver
Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1080/00397911.2015.1021426
Artigo de periodico
Synthesis of some functionalized peptomers via UGI four-component reaction (2015)
Silva, Eduardo H. B; Emery, Flavio da Silva; Del Ponte, Gino; Donate, Paulo Marcos
Source: Synthetic Communications. Unidades: FCFRP, FFCLRP
Subjects: PEPTÍDEOS, SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Eduardo H. B et al. Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, v. 45, n. 15, p. 1761-1767, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1042591. Acesso em: 05 dez. 2025.
APA
Silva, E. H. B., Emery, F. da S., Del Ponte, G., & Donate, P. M. (2015). Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, 45( 15), 1761-1767. doi:10.1080/00397911.2015.1042591
NLM
Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
Vancouver
Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
Artigo de periodico
Synthesis of analogues of thyroid hormones: nuclear receptor modulators (2015)
Castro, Guilherme Vieira de; Rocha, Carlos Murilo Romero; Sanches, Vitor Lacerda; Ribeiro, Pedro H. Zana; Donate, Paulo Marcos; Laurentiz, Rosangela da Silva de; Polikarpov, Igor ; Sairre, Mirela I.
Source: Orbital. Unidades: FFCLRP, IFSC
Subjects: HORMÔNIOS TIREOIDIANOS, LIGANTES, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Guilherme Vieira de et al. Synthesis of analogues of thyroid hormones: nuclear receptor modulators. Orbital, v. 7, n. 3, p. 281-291, 2015Tradução . . Disponível em: https://doi.org/10.17807/orbital.v7i3.739. Acesso em: 05 dez. 2025.
APA
Castro, G. V. de, Rocha, C. M. R., Sanches, V. L., Ribeiro, P. H. Z., Donate, P. M., Laurentiz, R. da S. de, et al. (2015). Synthesis of analogues of thyroid hormones: nuclear receptor modulators. Orbital, 7( 3), 281-291. doi:10.17807/orbital.v7i3.739
NLM
Castro GV de, Rocha CMR, Sanches VL, Ribeiro PHZ, Donate PM, Laurentiz R da S de, Polikarpov I, Sairre MI. Synthesis of analogues of thyroid hormones: nuclear receptor modulators [Internet]. Orbital. 2015 ; 7( 3): 281-291.[citado 2025 dez. 05 ] Available from: https://doi.org/10.17807/orbital.v7i3.739
Vancouver
Castro GV de, Rocha CMR, Sanches VL, Ribeiro PHZ, Donate PM, Laurentiz R da S de, Polikarpov I, Sairre MI. Synthesis of analogues of thyroid hormones: nuclear receptor modulators [Internet]. Orbital. 2015 ; 7( 3): 281-291.[citado 2025 dez. 05 ] Available from: https://doi.org/10.17807/orbital.v7i3.739
Artigo de periodico
Convenient synthesis of ketal derivatives from cubebin using amberlite as heterogeneous catalyst (2015)
Laurentiz, Rosangela da Silva de; Borges, Alexandre; Silva, Marcio Luis Andrade e; Donate, Paulo Marcos
Source: Chemistry of Natural Compounds. Unidade: FFCLRP
Subjects: PRODUTOS NATURAIS, CATÁLISE, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAURENTIZ, Rosangela da Silva de et al. Convenient synthesis of ketal derivatives from cubebin using amberlite as heterogeneous catalyst. Chemistry of Natural Compounds, v. 51, n. 1, p. 34-39, 2015Tradução . . Disponível em: https://doi.org/10.1007/s10600-015-1197-8. Acesso em: 05 dez. 2025.
APA
Laurentiz, R. da S. de, Borges, A., Silva, M. L. A. e, & Donate, P. M. (2015). Convenient synthesis of ketal derivatives from cubebin using amberlite as heterogeneous catalyst. Chemistry of Natural Compounds, 51( 1), 34-39. doi:10.1007/s10600-015-1197-8
NLM
Laurentiz R da S de, Borges A, Silva MLA e, Donate PM. Convenient synthesis of ketal derivatives from cubebin using amberlite as heterogeneous catalyst [Internet]. Chemistry of Natural Compounds. 2015 ; 51( 1): 34-39.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1007/s10600-015-1197-8
Vancouver
Laurentiz R da S de, Borges A, Silva MLA e, Donate PM. Convenient synthesis of ketal derivatives from cubebin using amberlite as heterogeneous catalyst [Internet]. Chemistry of Natural Compounds. 2015 ; 51( 1): 34-39.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1007/s10600-015-1197-8
Artigo de periodico
Green synthesis from biomass (2014)
Donate, Paulo Marcos
Source: Chemical and Biological Technologies in Agriculture. Unidade: FFCLRP
Subjects: QUÍMICA VERDE, SÍNTESE QUÍMICA, BIOMASSA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DONATE, Paulo Marcos. Green synthesis from biomass. Chemical and Biological Technologies in Agriculture, v. 1, 2014Tradução . . Disponível em: https://doi.org/10.1186/s40538-014-0004-2. Acesso em: 05 dez. 2025.
APA
Donate, P. M. (2014). Green synthesis from biomass. Chemical and Biological Technologies in Agriculture, 1. doi:10.1186/s40538-014-0004-2
NLM
Donate PM. Green synthesis from biomass [Internet]. Chemical and Biological Technologies in Agriculture. 2014 ; 1[citado 2025 dez. 05 ] Available from: https://doi.org/10.1186/s40538-014-0004-2
Vancouver
Donate PM. Green synthesis from biomass [Internet]. Chemical and Biological Technologies in Agriculture. 2014 ; 1[citado 2025 dez. 05 ] Available from: https://doi.org/10.1186/s40538-014-0004-2

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