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Artigo de periodico
Antitumor Activity of New Pd(II) Complexes with Ligands Derived from O-Vanillin Acting as Topoisomerase I and II Inhibitors (2024)
Franco, Mariane A.; Guedes, Adriana P. M.; Batista, Alzir A.; Deflon, Victor Marcelo ; Akinyemi, Amos O.; Rocha, Josias S.; Rocha, Fillipe V.
Source: ChemistrySelect. Unidade: IQSC
Assunto: ENZIMAS
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ABNT
FRANCO, Mariane A. et al. Antitumor Activity of New Pd(II) Complexes with Ligands Derived from O-Vanillin Acting as Topoisomerase I and II Inhibitors. ChemistrySelect, v. 9, p. e202402328, 2024Tradução . . Disponível em: https://doi.org/10.1002/slct.202402328. Acesso em: 27 nov. 2025.
APA
Franco, M. A., Guedes, A. P. M., Batista, A. A., Deflon, V. M., Akinyemi, A. O., Rocha, J. S., & Rocha, F. V. (2024). Antitumor Activity of New Pd(II) Complexes with Ligands Derived from O-Vanillin Acting as Topoisomerase I and II Inhibitors. ChemistrySelect, 9, e202402328. doi:10.1002/slct.202402328
NLM
Franco MA, Guedes APM, Batista AA, Deflon VM, Akinyemi AO, Rocha JS, Rocha FV. Antitumor Activity of New Pd(II) Complexes with Ligands Derived from O-Vanillin Acting as Topoisomerase I and II Inhibitors [Internet]. ChemistrySelect. 2024 ;9 e202402328.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202402328
Vancouver
Franco MA, Guedes APM, Batista AA, Deflon VM, Akinyemi AO, Rocha JS, Rocha FV. Antitumor Activity of New Pd(II) Complexes with Ligands Derived from O-Vanillin Acting as Topoisomerase I and II Inhibitors [Internet]. ChemistrySelect. 2024 ;9 e202402328.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202402328
Artigo de periodico
Synthesis, Structural Characterization, X-ray, Hirshfeld Surfaces, DFT calculations, In Silico ADME Approach and a Molecular Docking Study of a New Nickel(II) Complex (2022)
Souza, Rafael Aparecido Carvalho; Cunha, Vito Labruna; Franca, Eduardo de Faria; Deflon, Victor Marcelo ; Maia, Pedro Ivo da Silva; Oliveira, Carolina Gonçalves
Source: ChemistrySelect. Unidade: IQSC
Subjects: RAIOS X, NÍQUEL, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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ABNT
SOUZA, Rafael Aparecido Carvalho et al. Synthesis, Structural Characterization, X-ray, Hirshfeld Surfaces, DFT calculations, In Silico ADME Approach and a Molecular Docking Study of a New Nickel(II) Complex. ChemistrySelect, v. 7, p. e202202409, 2022Tradução . . Disponível em: https://doi.org/10.1002/slct.202202409. Acesso em: 27 nov. 2025.
APA
Souza, R. A. C., Cunha, V. L., Franca, E. de F., Deflon, V. M., Maia, P. I. da S., & Oliveira, C. G. (2022). Synthesis, Structural Characterization, X-ray, Hirshfeld Surfaces, DFT calculations, In Silico ADME Approach and a Molecular Docking Study of a New Nickel(II) Complex. ChemistrySelect, 7, e202202409. doi:10.1002/slct.202202409
NLM
Souza RAC, Cunha VL, Franca E de F, Deflon VM, Maia PI da S, Oliveira CG. Synthesis, Structural Characterization, X-ray, Hirshfeld Surfaces, DFT calculations, In Silico ADME Approach and a Molecular Docking Study of a New Nickel(II) Complex [Internet]. ChemistrySelect. 2022 ;7 e202202409.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202202409
Vancouver
Souza RAC, Cunha VL, Franca E de F, Deflon VM, Maia PI da S, Oliveira CG. Synthesis, Structural Characterization, X-ray, Hirshfeld Surfaces, DFT calculations, In Silico ADME Approach and a Molecular Docking Study of a New Nickel(II) Complex [Internet]. ChemistrySelect. 2022 ;7 e202202409.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202202409
Artigo de periodico
Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate (2021)
Lima, Rafaely Nascimento ; Vaz, Artur de Lara Lima ; Clososki, Giuliano Cesar ; Porto, Andre Luiz Meleiro
Source: ChemistrySelect. Unidades: FCFRP, IQSC
Assunto: QUÍMICA VERDE
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ABNT
LIMA, Rafaely Nascimento et al. Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate. ChemistrySelect, v. 6, p. 21, 2021Tradução . . Disponível em: https://doi.org/10.1002/slct.202100883. Acesso em: 27 nov. 2025.
APA
Lima, R. N., Vaz, A. de L. L., Clososki, G. C., & Porto, A. L. M. (2021). Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate. ChemistrySelect, 6, 21. doi:10.1002/slct.202100883
NLM
Lima RN, Vaz A de LL, Clososki GC, Porto ALM. Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate [Internet]. ChemistrySelect. 2021 ;6 21.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202100883
Vancouver
Lima RN, Vaz A de LL, Clososki GC, Porto ALM. Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate [Internet]. ChemistrySelect. 2021 ;6 21.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202100883
Artigo de periodico
Gellan-Gum and LiTFSI-Based Solid Polymer Electrolytes for Electrochromic Devices (2021)
Isfahani, Vahideh Bayzi; Pereira, Rui F P; Fernandes, Mariana; Sabadini, Rodrigo Cesar ; Pereira, Sónia; Dizaji, Hamid Rezagholipour; Arab, Ali; Fortunato, Elvira ; Pawlicka, Agnieszka ; Rego, Rosa; Bermudez, Verónica de Zea; Silva, Maria Manuela
Source: ChemistrySelect. Unidade: IQSC
Subjects: POLÍMEROS (MATERIAIS), ELETRÓLITOS
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ABNT
ISFAHANI, Vahideh Bayzi et al. Gellan-Gum and LiTFSI-Based Solid Polymer Electrolytes for Electrochromic Devices. ChemistrySelect, v. 6, n. 20, p. 5110-5119, 2021Tradução . . Disponível em: https://doi.org/10.1002/slct.202004614. Acesso em: 27 nov. 2025.
APA
Isfahani, V. B., Pereira, R. F. P., Fernandes, M., Sabadini, R. C., Pereira, S., Dizaji, H. R., et al. (2021). Gellan-Gum and LiTFSI-Based Solid Polymer Electrolytes for Electrochromic Devices. ChemistrySelect, 6( 20), 5110-5119. doi:10.1002/slct.202004614
NLM
Isfahani VB, Pereira RFP, Fernandes M, Sabadini RC, Pereira S, Dizaji HR, Arab A, Fortunato E, Pawlicka A, Rego R, Bermudez V de Z, Silva MM. Gellan-Gum and LiTFSI-Based Solid Polymer Electrolytes for Electrochromic Devices [Internet]. ChemistrySelect. 2021 ;6( 20): 5110-5119.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202004614
Vancouver
Isfahani VB, Pereira RFP, Fernandes M, Sabadini RC, Pereira S, Dizaji HR, Arab A, Fortunato E, Pawlicka A, Rego R, Bermudez V de Z, Silva MM. Gellan-Gum and LiTFSI-Based Solid Polymer Electrolytes for Electrochromic Devices [Internet]. ChemistrySelect. 2021 ;6( 20): 5110-5119.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202004614
Artigo de periodico
HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions (2020)
Zanin, Lucas Lima ; Porto, Andre Luiz Meleiro
Source: ChemistrySelect. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, CATALISADORES
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ABNT
ZANIN, Lucas Lima e PORTO, Andre Luiz Meleiro. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, v. 5, n. 28, p. 8604-8608, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202001830. Acesso em: 27 nov. 2025.
APA
Zanin, L. L., & Porto, A. L. M. (2020). HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, 5( 28), 8604-8608. doi:10.1002/slct.202001830
NLM
Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202001830
Vancouver
Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202001830
Artigo de periodico
Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry (2020)
Khalid, Muhammad ; Ali, Akbar ; Abid , Saba; Tahir, Muhammad Nawaz; Khan, Muhammad Usman ; Ashfaq, Muhammad; Imran, Muhammad; Ahmad, Anees
Source: ChemistrySelect. Unidade: IQSC
Subjects: ULTRASSOM, RAIOS X
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ABNT
KHALID, Muhammad et al. Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry. ChemistrySelect, v. 5, p. , 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202003589. Acesso em: 27 nov. 2025.
APA
Khalid, M., Ali, A., Abid , S., Tahir, M. N., Khan, M. U., Ashfaq, M., et al. (2020). Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry. ChemistrySelect, 5, . doi:10.1002/slct.202003589
NLM
Khalid M, Ali A, Abid S, Tahir MN, Khan MU, Ashfaq M, Imran M, Ahmad A. Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry [Internet]. ChemistrySelect. 2020 ; 5 .[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202003589
Vancouver
Khalid M, Ali A, Abid S, Tahir MN, Khan MU, Ashfaq M, Imran M, Ahmad A. Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry [Internet]. ChemistrySelect. 2020 ; 5 .[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202003589
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: 27 nov. 2025.
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 2025 nov. 27 ] 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 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.202004340
Artigo de periodico
Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities (2018)
Metzker, Gustavo; Dias, Rafael Mafra de Paula; Burtoloso, Antonio Carlos Bender
Source: ChemistrySelect. Unidade: IQSC
Assunto: BIOMASSA
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ABNT
METZKER, Gustavo e DIAS, Rafael Mafra de Paula e BURTOLOSO, Antonio Carlos Bender. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities. ChemistrySelect, v. 3, n. 2, p. 368-372, 2018Tradução . . Disponível em: https://doi.org/10.1002/slct.201702580. Acesso em: 27 nov. 2025.
APA
Metzker, G., Dias, R. M. de P., & Burtoloso, A. C. B. (2018). Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities. ChemistrySelect, 3( 2), 368-372. doi:10.1002/slct.201702580
NLM
Metzker G, Dias RM de P, Burtoloso ACB. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities [Internet]. ChemistrySelect. 2018 ; 3( 2): 368-372.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.201702580
Vancouver
Metzker G, Dias RM de P, Burtoloso ACB. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities [Internet]. ChemistrySelect. 2018 ; 3( 2): 368-372.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1002/slct.201702580

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