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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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ABNT
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
ESR dosimetry with lithium, potassium, and sodium compounds (2022)
Rech, Amanda B.; Kinoshita, Angela; Donate, Paulo Marcos ; Baffa, Oswaldo
Source: Applied Radiation and Isotopes. Unidade: FFCLRP
Subjects: DOSIMETRIA, RESSONÂNCIA PARAMAGNÉTICA DE SPIN, DOSÍMETROS, LÍTIO, POTÁSSIO, SÓDIO
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ABNT
RECH, Amanda B. et al. ESR dosimetry with lithium, potassium, and sodium compounds. Applied Radiation and Isotopes, v. 181, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.apradiso.2022.110105. Acesso em: 05 dez. 2025.
APA
Rech, A. B., Kinoshita, A., Donate, P. M., & Baffa, O. (2022). ESR dosimetry with lithium, potassium, and sodium compounds. Applied Radiation and Isotopes, 181. doi:10.1016/j.apradiso.2022.110105
NLM
Rech AB, Kinoshita A, Donate PM, Baffa O. ESR dosimetry with lithium, potassium, and sodium compounds [Internet]. Applied Radiation and Isotopes. 2022 ; 181[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.apradiso.2022.110105
Vancouver
Rech AB, Kinoshita A, Donate PM, Baffa O. ESR dosimetry with lithium, potassium, and sodium compounds [Internet]. Applied Radiation and Isotopes. 2022 ; 181[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.apradiso.2022.110105
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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ABNT
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
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
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
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
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
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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
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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
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
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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

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