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Artigo de periodico
Oxidation products from the neolignan licarin A by biomimetic reactions and assessment of in vivo acute toxicity (2023)
Souza, Juliana Neves de Paula e; Silva, Rodrigo Moreira da ; Fortes, Simone Silveira; Oliveira, Anderson Rodrigo Moraes de ; Ferreira, Leandro S.; Vessecchi, Ricardo ; Lopes, Norberto Peporine ; Silva, Denise Brentan da
Fonte: Planta Medica. Unidades: FCFRP, FFCLRP
Assuntos: CATALISADORES, POLIFENÓIS, FÍGADO, OXIDAÇÃO
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SOUZA, Juliana Neves de Paula e et al. Oxidation products from the neolignan licarin A by biomimetic reactions and assessment of in vivo acute toxicity. Planta Medica, v. 89, n. 7, p. 700-708, 2023Tradução . . Disponível em: https://doi.org/10.1055/a-2009-0732. Acesso em: 23 jul. 2024.
APA
Souza, J. N. de P. e, Silva, R. M. da, Fortes, S. S., Oliveira, A. R. M. de, Ferreira, L. S., Vessecchi, R., et al. (2023). Oxidation products from the neolignan licarin A by biomimetic reactions and assessment of in vivo acute toxicity. Planta Medica, 89( 7), 700-708. doi:10.1055/a-2009-0732
NLM
Souza JN de P e, Silva RM da, Fortes SS, Oliveira ARM de, Ferreira LS, Vessecchi R, Lopes NP, Silva DB da. Oxidation products from the neolignan licarin A by biomimetic reactions and assessment of in vivo acute toxicity [Internet]. Planta Medica. 2023 ; 89( 7): 700-708.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1055/a-2009-0732
Vancouver
Souza JN de P e, Silva RM da, Fortes SS, Oliveira ARM de, Ferreira LS, Vessecchi R, Lopes NP, Silva DB da. Oxidation products from the neolignan licarin A by biomimetic reactions and assessment of in vivo acute toxicity [Internet]. Planta Medica. 2023 ; 89( 7): 700-708.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1055/a-2009-0732
Artigo de periodico
Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry (2023)
Borges, Letícia da Silva; Batista, João Henrique Carvalho; Bozzini, Leandro Alves ; Lourenço Júnior, Celso Donizete; Lopes, Norberto Peporine ; Clososki, Giuliano Cesar ; Vessecchi, Ricardo
Fonte: Rapid Communications in Mass Spectrometry. Unidades: FCFRP, FFCLRP
Assuntos: ÍONS, MECÂNICA QUÂNTICA, ESPECTROMETRIA DE MASSAS
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BORGES, Letícia da Silva et al. Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry. Rapid Communications in Mass Spectrometry, v. 37, n. 4, p. 1-11, 2023Tradução . . Disponível em: https://doi.org/10.1002/rcm.9449. Acesso em: 23 jul. 2024.
APA
Borges, L. da S., Batista, J. H. C., Bozzini, L. A., Lourenço Júnior, C. D., Lopes, N. P., Clososki, G. C., & Vessecchi, R. (2023). Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry. Rapid Communications in Mass Spectrometry, 37( 4), 1-11. doi:10.1002/rcm.9449
NLM
Borges L da S, Batista JHC, Bozzini LA, Lourenço Júnior CD, Lopes NP, Clososki GC, Vessecchi R. Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry [Internet]. Rapid Communications in Mass Spectrometry. 2023 ; 37( 4): 1-11.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/rcm.9449
Vancouver
Borges L da S, Batista JHC, Bozzini LA, Lourenço Júnior CD, Lopes NP, Clososki GC, Vessecchi R. Are benzoylium and nitrilium ions produced from substituted 2‐arene‐2‐oxazolines during mass spectrometry?: a study based on density functional theory calculations, quantum theory of atoms in molecules, and electrospray ionization tandem mass spectrometry [Internet]. Rapid Communications in Mass Spectrometry. 2023 ; 37( 4): 1-11.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/rcm.9449
Artigo de periodico
Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases (2021)
Santos, Thiago dos ; Orenha, Henrique Pereira; Murie, Valter Eduardo ; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Fonte: Organic Letters. Unidades: FFCLRP, FCFRP
Assuntos: COMPOSTOS DE NITROGÊNIO, NITRILAS, QUÍMICA ORGÂNICA, COMPOSTOS HETEROCÍCLICOS
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SANTOS, Thiago dos et al. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, v. 23, n. 19, p. 7396-7400, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c02572. Acesso em: 23 jul. 2024.
APA
Santos, T. dos, Orenha, H. P., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2021). Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, 23( 19), 7396-7400. doi:10.1021/acs.orglett.1c02572
NLM
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Vancouver
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Artigo de periodico
Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides (2021)
Bozzini, Leandro Alves; Santos, Thiago dos ; Murie, Valter Eduardo ; Mello, Murilo B. M.; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Fonte: The Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP
Assuntos: COMPOSTOS HETEROCÍCLICOS, QUÍMICA MÉDICA, PRODUTOS NATURAIS, MEDICAMENTO
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BOZZINI, Leandro Alves et al. Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides. The Journal of Organic Chemistry, v. 86, n. 1, p. 1204-1215, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.0c02369. Acesso em: 23 jul. 2024.
APA
Bozzini, L. A., Santos, T. dos, Murie, V. E., Mello, M. B. M., Vessecchi, R., & Clososki, G. C. (2021). Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides. The Journal of Organic Chemistry, 86( 1), 1204-1215. doi:10.1021/acs.joc.0c02369
NLM
Bozzini LA, Santos T dos, Murie VE, Mello MBM, Vessecchi R, Clososki GC. Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 1): 1204-1215.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1021/acs.joc.0c02369
Vancouver
Bozzini LA, Santos T dos, Murie VE, Mello MBM, Vessecchi R, Clososki GC. Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 1): 1204-1215.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1021/acs.joc.0c02369
Artigo de periodico
Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations (2020)
Nishimura, Rodolfo Hideki Vicente ; Murie, Valter Eduardo ; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Fonte: ChemistrySelect. Unidades: FFCLRP, FCFRP
Assuntos: METALIZAÇÃO, COMPOSTOS ORGANOMETÁLICOS, QUÍMICA MÉDICA, SÍNTESE ORGÂNICA, AMIDAS
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NISHIMURA, Rodolfo Hideki Vicente et al. Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations. ChemistrySelect, v. 5, n. 36, p. 11106-11111, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202002589. Acesso em: 23 jul. 2024.
APA
Nishimura, R. H. V., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2020). Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations. ChemistrySelect, 5( 36), 11106-11111. doi:10.1002/slct.202002589
NLM
Nishimura RHV, Murie VE, Vessecchi R, Clososki GC. Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations [Internet]. ChemistrySelect. 2020 ; 5( 36): 11106-11111.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/slct.202002589
Vancouver
Nishimura RHV, Murie VE, Vessecchi R, Clososki GC. Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations [Internet]. ChemistrySelect. 2020 ; 5( 36): 11106-11111.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/slct.202002589
Artigo de periodico
Electrospray ionization tandem mass spectrometry of monoketone curcuminoids (2020)
Vieira, Tatiana Manzini ; Orenha, Renato Pereira; Crevelin, Eduardo José ; Furtado, Saulo S. P.; Vessecchi, Ricardo ; Parreira, Renato L. T.; Crotti, Antonio Eduardo Miller
Fonte: Rapid Communications in Mass Spectrometry. Unidade: FFCLRP
Assuntos: ESPECTROMETRIA DE MASSAS, ÍONS, DEUTÉRIO, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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VIEIRA, Tatiana Manzini et al. Electrospray ionization tandem mass spectrometry of monoketone curcuminoids. Rapid Communications in Mass Spectrometry, v. 34, 2020Tradução . . Disponível em: https://doi.org/10.1002/rcm.8699. Acesso em: 23 jul. 2024.
APA
Vieira, T. M., Orenha, R. P., Crevelin, E. J., Furtado, S. S. P., Vessecchi, R., Parreira, R. L. T., & Crotti, A. E. M. (2020). Electrospray ionization tandem mass spectrometry of monoketone curcuminoids. Rapid Communications in Mass Spectrometry, 34. doi:10.1002/rcm.8699
NLM
Vieira TM, Orenha RP, Crevelin EJ, Furtado SSP, Vessecchi R, Parreira RLT, Crotti AEM. Electrospray ionization tandem mass spectrometry of monoketone curcuminoids [Internet]. Rapid Communications in Mass Spectrometry. 2020 ; 34[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/rcm.8699
Vancouver
Vieira TM, Orenha RP, Crevelin EJ, Furtado SSP, Vessecchi R, Parreira RLT, Crotti AEM. Electrospray ionization tandem mass spectrometry of monoketone curcuminoids [Internet]. Rapid Communications in Mass Spectrometry. 2020 ; 34[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/rcm.8699
Artigo de periodico
Gas-phase fragmentation reactions of protonated benzofuran- and dihydrobenzofuran-type neolignans investigated by accurate-mass electrospray ionization tandem mass spectrometry (2019)
Dias, Herbert Júnior; Baguenard, Manon; Crevelin, Eduardo José ; Palaretti, Vinicius; Gates, Paul J.; Vessecchi, Ricardo ; Crotti, Antonio Eduardo Miller
Fonte: Journal of Mass Spectrometry. Unidade: FFCLRP
Assuntos: COMPUTAÇÃO APLICADA, QUÍMICA, ESPECTROMETRIA DE MASSAS, IONIZAÇÃO DE GASES
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DIAS, Herbert Júnior et al. Gas-phase fragmentation reactions of protonated benzofuran- and dihydrobenzofuran-type neolignans investigated by accurate-mass electrospray ionization tandem mass spectrometry. Journal of Mass Spectrometry, v. 54, n. 1, p. 35-46, 2019Tradução . . Disponível em: https://doi.org/10.1002/jms.4304. Acesso em: 23 jul. 2024.
APA
Dias, H. J., Baguenard, M., Crevelin, E. J., Palaretti, V., Gates, P. J., Vessecchi, R., & Crotti, A. E. M. (2019). Gas-phase fragmentation reactions of protonated benzofuran- and dihydrobenzofuran-type neolignans investigated by accurate-mass electrospray ionization tandem mass spectrometry. Journal of Mass Spectrometry, 54( 1), 35-46. doi:10.1002/jms.4304
NLM
Dias HJ, Baguenard M, Crevelin EJ, Palaretti V, Gates PJ, Vessecchi R, Crotti AEM. Gas-phase fragmentation reactions of protonated benzofuran- and dihydrobenzofuran-type neolignans investigated by accurate-mass electrospray ionization tandem mass spectrometry [Internet]. Journal of Mass Spectrometry. 2019 ; 54( 1): 35-46.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4304
Vancouver
Dias HJ, Baguenard M, Crevelin EJ, Palaretti V, Gates PJ, Vessecchi R, Crotti AEM. Gas-phase fragmentation reactions of protonated benzofuran- and dihydrobenzofuran-type neolignans investigated by accurate-mass electrospray ionization tandem mass spectrometry [Internet]. Journal of Mass Spectrometry. 2019 ; 54( 1): 35-46.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4304
Artigo de periodico
C-H activation/metalation approaches for the synthesis of indolizine derivatives (2019)
Bertallo, Camila Rodrigues de Souza ; Arroio, Thais Rodrigues ; Toledo, Mônica Franco Zannini Junqueira; Sadler, Scott A.; Vessecchi, Ricardo ; Steel, Patrick G.; Clososki, Giuliano Cesar
Fonte: European Journal of Organic Chemistry. Unidades: FCF, FFCLRP, FCFRP
Assuntos: COMPOSTOS ORGÂNICOS, AROMATIZANTES, SÍNTESE QUÍMICA
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BERTALLO, Camila Rodrigues de Souza et al. C-H activation/metalation approaches for the synthesis of indolizine derivatives. European Journal of Organic Chemistry, v. 2019, n. 31-32, p. 5205-5213, 2019Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201900608. Acesso em: 23 jul. 2024.
APA
Bertallo, C. R. de S., Arroio, T. R., Toledo, M. F. Z. J., Sadler, S. A., Vessecchi, R., Steel, P. G., & Clososki, G. C. (2019). C-H activation/metalation approaches for the synthesis of indolizine derivatives. European Journal of Organic Chemistry, 2019( 31-32), 5205-5213. doi:10.1002/ejoc.201900608
NLM
Bertallo CR de S, Arroio TR, Toledo MFZJ, Sadler SA, Vessecchi R, Steel PG, Clososki GC. C-H activation/metalation approaches for the synthesis of indolizine derivatives [Internet]. European Journal of Organic Chemistry. 2019 ; 2019( 31-32): 5205-5213.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/ejoc.201900608
Vancouver
Bertallo CR de S, Arroio TR, Toledo MFZJ, Sadler SA, Vessecchi R, Steel PG, Clososki GC. C-H activation/metalation approaches for the synthesis of indolizine derivatives [Internet]. European Journal of Organic Chemistry. 2019 ; 2019( 31-32): 5205-5213.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/ejoc.201900608
Artigo de periodico
Combined use of tandem mass spectrometry and computational chemistry to study 2H-chromenes from Piper aduncum (2019)
Souza, Amauri Alves; Vessecchi, Ricardo ; Castro-Gamboa, Ian; Furlan, Maysa
Fonte: Journal of Mass Spectrometry. Unidade: FFCLRP
Assuntos: QUÍMICA, COMPUTAÇÃO APLICADA, DENSIDADE, ESPECTROMETRIA DE MASSAS
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SOUZA, Amauri Alves et al. Combined use of tandem mass spectrometry and computational chemistry to study 2H-chromenes from Piper aduncum. Journal of Mass Spectrometry, v. 54, n. 7, p. 634-642, 2019Tradução . . Disponível em: https://doi.org/10.1002/jms.4378. Acesso em: 23 jul. 2024.
APA
Souza, A. A., Vessecchi, R., Castro-Gamboa, I., & Furlan, M. (2019). Combined use of tandem mass spectrometry and computational chemistry to study 2H-chromenes from Piper aduncum. Journal of Mass Spectrometry, 54( 7), 634-642. doi:10.1002/jms.4378
NLM
Souza AA, Vessecchi R, Castro-Gamboa I, Furlan M. Combined use of tandem mass spectrometry and computational chemistry to study 2H-chromenes from Piper aduncum [Internet]. Journal of Mass Spectrometry. 2019 ; 54( 7): 634-642.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4378
Vancouver
Souza AA, Vessecchi R, Castro-Gamboa I, Furlan M. Combined use of tandem mass spectrometry and computational chemistry to study 2H-chromenes from Piper aduncum [Internet]. Journal of Mass Spectrometry. 2019 ; 54( 7): 634-642.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4378
Artigo de periodico
Characterization of aporphine alkaloids by electrospray ionization tandem mass spectrometry and density functional theory calculations (2019)
Carnevale Neto, Fausto; Andréo, Márcio Adriano; Raftery, Daniel; Lopes, João Luis Callegari ; Lopes, Norberto Peporine ; Castro-Gamboa, Ian; Maia, Beatriz Helena Lameiro Noronha Salles; Costa, Emmanoel Vilaça; Vessecchi, Ricardo
Fonte: Rapid Communications in Mass Spectrometry. Unidades: FCFRP, FFCLRP
Assuntos: ALCALOIDES, ESPECTROMETRIA DE MASSAS, PRODUTOS NATURAIS, ÍONS
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CARNEVALE NETO, Fausto et al. Characterization of aporphine alkaloids by electrospray ionization tandem mass spectrometry and density functional theory calculations. Rapid Communications in Mass Spectrometry, v. 34, 2019Tradução . . Disponível em: https://doi.org/10.1002/rcm.8533. Acesso em: 23 jul. 2024.
APA
Carnevale Neto, F., Andréo, M. A., Raftery, D., Lopes, J. L. C., Lopes, N. P., Castro-Gamboa, I., et al. (2019). Characterization of aporphine alkaloids by electrospray ionization tandem mass spectrometry and density functional theory calculations. Rapid Communications in Mass Spectrometry, 34. doi:10.1002/rcm.8533
NLM
Carnevale Neto F, Andréo MA, Raftery D, Lopes JLC, Lopes NP, Castro-Gamboa I, Maia BHLNS, Costa EV, Vessecchi R. Characterization of aporphine alkaloids by electrospray ionization tandem mass spectrometry and density functional theory calculations [Internet]. Rapid Communications in Mass Spectrometry. 2019 ; 34[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/rcm.8533
Vancouver
Carnevale Neto F, Andréo MA, Raftery D, Lopes JLC, Lopes NP, Castro-Gamboa I, Maia BHLNS, Costa EV, Vessecchi R. Characterization of aporphine alkaloids by electrospray ionization tandem mass spectrometry and density functional theory calculations [Internet]. Rapid Communications in Mass Spectrometry. 2019 ; 34[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/rcm.8533
Artigo de periodico
Elucidating the mass spectrum of the retronecine alkaloid using DFT calculations (2018)
Modesto-Costa, Lucas ; Martinez, Sabrina T.; Pinto, Angelo da Cunha; Vessecchi, Ricardo ; Borges Júnior, Itamar
Fonte: Journal of Mass Spectrometry. Unidade: FFCLRP
Assuntos: COMPUTAÇÃO APLICADA, QUÍMICA, ESPECTROMETRIA DE MASSAS
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ABNT
MODESTO-COSTA, Lucas et al. Elucidating the mass spectrum of the retronecine alkaloid using DFT calculations. Journal of Mass Spectrometry, v. 53, n. 10, p. 934-941, 2018Tradução . . Disponível em: https://doi.org/10.1002/jms.4253. Acesso em: 23 jul. 2024.
APA
Modesto-Costa, L., Martinez, S. T., Pinto, A. da C., Vessecchi, R., & Borges Júnior, I. (2018). Elucidating the mass spectrum of the retronecine alkaloid using DFT calculations. Journal of Mass Spectrometry, 53( 10), 934-941. doi:10.1002/jms.4253
NLM
Modesto-Costa L, Martinez ST, Pinto A da C, Vessecchi R, Borges Júnior I. Elucidating the mass spectrum of the retronecine alkaloid using DFT calculations [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 10): 934-941.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4253
Vancouver
Modesto-Costa L, Martinez ST, Pinto A da C, Vessecchi R, Borges Júnior I. Elucidating the mass spectrum of the retronecine alkaloid using DFT calculations [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 10): 934-941.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4253
Artigo de periodico
Gas-phase fragmentation reactions of protonated cocaine: new details to an old story (2018)
Dias, Herbert Júnior ; Bento, Mariana Vilas Boas; Silva, Eder Henrique da ; Saturnino Júnior, Andrade; Oliveira, Marcelo Firmino de ; Vessecchi, Ricardo ; Parreira, Renato Luis Tâme ; Crotti, Antonio Eduardo Miller
Fonte: Journal of Mass Spectrometry. Unidade: FFCLRP
Assuntos: COCAÍNA, ÍONS, REAÇÕES À SEPARAÇÃO
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ABNT
DIAS, Herbert Júnior et al. Gas-phase fragmentation reactions of protonated cocaine: new details to an old story. Journal of Mass Spectrometry, v. 53, n. 3, p. 203-213, 2018Tradução . . Disponível em: https://doi.org/10.1002/jms.4053. Acesso em: 23 jul. 2024.
APA
Dias, H. J., Bento, M. V. B., Silva, E. H. da, Saturnino Júnior, A., Oliveira, M. F. de, Vessecchi, R., et al. (2018). Gas-phase fragmentation reactions of protonated cocaine: new details to an old story. Journal of Mass Spectrometry, 53( 3), 203-213. doi:10.1002/jms.4053
NLM
Dias HJ, Bento MVB, Silva EH da, Saturnino Júnior A, Oliveira MF de, Vessecchi R, Parreira RLT, Crotti AEM. Gas-phase fragmentation reactions of protonated cocaine: new details to an old story [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 3): 203-213.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4053
Vancouver
Dias HJ, Bento MVB, Silva EH da, Saturnino Júnior A, Oliveira MF de, Vessecchi R, Parreira RLT, Crotti AEM. Gas-phase fragmentation reactions of protonated cocaine: new details to an old story [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 3): 203-213.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4053
Artigo de periodico
Electrospray ionization tandem mass spectrometry of labdane-type acid diterpenes (2018)
Aguiar, Gabriela de Paula; Crevelin, Eduardo José ; Dias, Herbert Júnior ; Ambrosio, Sérgio Ricardo; Bastos, Jairo Kenupp; Heleno, Vladimir Constantino Gomes ; Vessecchi, Ricardo ; Crotti, Antonio Eduardo Miller
Fonte: Journal of Mass Spectrometry. Unidades: FFCLRP, FCFRP
Assuntos: CROMATOGRAFIA LÍQUIDA DE ALTA PRESSÃO, FABACEAE, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA), ESPECTROSCOPIA DE MASSA
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AGUIAR, Gabriela de Paula et al. Electrospray ionization tandem mass spectrometry of labdane-type acid diterpenes. Journal of Mass Spectrometry, v. 53, n. 11, p. 1086-1096, 2018Tradução . . Disponível em: https://doi.org/10.1002/jms.4284. Acesso em: 23 jul. 2024.
APA
Aguiar, G. de P., Crevelin, E. J., Dias, H. J., Ambrosio, S. R., Bastos, J. K., Heleno, V. C. G., et al. (2018). Electrospray ionization tandem mass spectrometry of labdane-type acid diterpenes. Journal of Mass Spectrometry, 53( 11), 1086-1096. doi:10.1002/jms.4284
NLM
Aguiar G de P, Crevelin EJ, Dias HJ, Ambrosio SR, Bastos JK, Heleno VCG, Vessecchi R, Crotti AEM. Electrospray ionization tandem mass spectrometry of labdane-type acid diterpenes [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 11): 1086-1096.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4284
Vancouver
Aguiar G de P, Crevelin EJ, Dias HJ, Ambrosio SR, Bastos JK, Heleno VCG, Vessecchi R, Crotti AEM. Electrospray ionization tandem mass spectrometry of labdane-type acid diterpenes [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 11): 1086-1096.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.4284
Artigo de periodico
Mass spectrometry analysis of protonated marine natural product seriniquinone (2018)
Silva, Rodrigo M. da; Guaratini, Thais; Jimenez, Paula C.; Fenical, William; Vessecchi, Ricardo; Lopes, Norberto Peporine; Lotufo, Leticia Veras Costa
Fonte: Journal Brazilian Chemical Society. Unidades: FFCLRP, FCFRP, ICB
Assuntos: COMPOSTOS AROMÁTICOS, METABÓLITOS, ESPECTROMETRIA DE MASSAS, IONIZAÇÃO DE GASES, BACTÉRIAS ANAERÓBICAS GRAM-POSITIVAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Rodrigo M. da et al. Mass spectrometry analysis of protonated marine natural product seriniquinone. Journal Brazilian Chemical Society, v. 29, n. 5, p. 1162-1166, 2018Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20180037. Acesso em: 23 jul. 2024.
APA
Silva, R. M. da, Guaratini, T., Jimenez, P. C., Fenical, W., Vessecchi, R., Lopes, N. P., & Lotufo, L. V. C. (2018). Mass spectrometry analysis of protonated marine natural product seriniquinone. Journal Brazilian Chemical Society, 29( 5), 1162-1166. doi:10.21577/0103-5053.20180037
NLM
Silva RM da, Guaratini T, Jimenez PC, Fenical W, Vessecchi R, Lopes NP, Lotufo LVC. Mass spectrometry analysis of protonated marine natural product seriniquinone [Internet]. Journal Brazilian Chemical Society. 2018 ; 29( 5): 1162-1166.[citado 2024 jul. 23 ] Available from: https://doi.org/10.21577/0103-5053.20180037
Vancouver
Silva RM da, Guaratini T, Jimenez PC, Fenical W, Vessecchi R, Lopes NP, Lotufo LVC. Mass spectrometry analysis of protonated marine natural product seriniquinone [Internet]. Journal Brazilian Chemical Society. 2018 ; 29( 5): 1162-1166.[citado 2024 jul. 23 ] Available from: https://doi.org/10.21577/0103-5053.20180037
Artigo de periodico
Conformational dynamics of 4-formylaminoantipyrine based on NMR and theoretical calculations (2018)
Silva, Simone Cavalcante; Rodrigues, Shirley Muniz Machado; Nardini, Viviani ; Vaz, Artur de Lara Lima ; Palaretti, Vinicius; Silva, Gil Valdo José da ; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Fonte: Journal of Molecular Structure. Unidades: FCFRP, FFCLRP
Assuntos: ESPECTROSCOPIA DE RESSONÂNCIA MAGNÉTICA NUCLEAR, METABÓLITOS, LIGAÇÕES QUÍMICAS, ISÔMERO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Simone Cavalcante et al. Conformational dynamics of 4-formylaminoantipyrine based on NMR and theoretical calculations. Journal of Molecular Structure, v. 1163, p. 280-286, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2018.03.003. Acesso em: 23 jul. 2024.
APA
Silva, S. C., Rodrigues, S. M. M., Nardini, V., Vaz, A. de L. L., Palaretti, V., Silva, G. V. J. da, et al. (2018). Conformational dynamics of 4-formylaminoantipyrine based on NMR and theoretical calculations. Journal of Molecular Structure, 1163, 280-286. doi:10.1016/j.molstruc.2018.03.003
NLM
Silva SC, Rodrigues SMM, Nardini V, Vaz A de LL, Palaretti V, Silva GVJ da, Vessecchi R, Clososki GC. Conformational dynamics of 4-formylaminoantipyrine based on NMR and theoretical calculations [Internet]. Journal of Molecular Structure. 2018 ; 1163 280-286.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.molstruc.2018.03.003
Vancouver
Silva SC, Rodrigues SMM, Nardini V, Vaz A de LL, Palaretti V, Silva GVJ da, Vessecchi R, Clososki GC. Conformational dynamics of 4-formylaminoantipyrine based on NMR and theoretical calculations [Internet]. Journal of Molecular Structure. 2018 ; 1163 280-286.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.molstruc.2018.03.003
Artigo de periodico
The influence of the negative hyperconjugation is relevant for the analysis of the π-π* conjugation with the mono-substitution and di-substitution of H2C= by O= and/or HN= in trans-buta-1,3-diene ? (2018)
Orenha, Renato Pereira ; Vessecchi, Ricardo ; Galembeck, Sérgio Emanuel
Fonte: Structural Chemistry. Unidade: FFCLRP
Assuntos: QUÍMICA ORGÂNICA, MODELAGEM MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ORENHA, Renato Pereira e VESSECCHI, Ricardo e GALEMBECK, Sérgio Emanuel. The influence of the negative hyperconjugation is relevant for the analysis of the π-π* conjugation with the mono-substitution and di-substitution of H2C= by O= and/or HN= in trans-buta-1,3-diene ?. Structural Chemistry, v. 29, n. 3, p. 847-857, 2018Tradução . . Disponível em: https://doi.org/10.1007/s11224-017-1070-4. Acesso em: 23 jul. 2024.
APA
Orenha, R. P., Vessecchi, R., & Galembeck, S. E. (2018). The influence of the negative hyperconjugation is relevant for the analysis of the π-π* conjugation with the mono-substitution and di-substitution of H2C= by O= and/or HN= in trans-buta-1,3-diene ? Structural Chemistry, 29( 3), 847-857. doi:10.1007/s11224-017-1070-4
NLM
Orenha RP, Vessecchi R, Galembeck SE. The influence of the negative hyperconjugation is relevant for the analysis of the π-π* conjugation with the mono-substitution and di-substitution of H2C= by O= and/or HN= in trans-buta-1,3-diene ? [Internet]. Structural Chemistry. 2018 ; 29( 3): 847-857.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1007/s11224-017-1070-4
Vancouver
Orenha RP, Vessecchi R, Galembeck SE. The influence of the negative hyperconjugation is relevant for the analysis of the π-π* conjugation with the mono-substitution and di-substitution of H2C= by O= and/or HN= in trans-buta-1,3-diene ? [Internet]. Structural Chemistry. 2018 ; 29( 3): 847-857.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1007/s11224-017-1070-4
Artigo de periodico
Base-controlled regioselective functionalization of chloro-substituted quinolines (2018)
Murie, Valter Eduardo ; Nishimura, Rodolfo Hideki Vicente ; Rolim, Larissa Araújo; Vessecchi, Ricardo ; Lopes, Norberto Peporine ; Clososki, Giuliano Cesar
Fonte: The Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP
Assuntos: PRODUTOS NATURAIS, SÍNTESE ORGÂNICA, QUÍMICA MÉDICA, REAÇÕES QUÍMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MURIE, Valter Eduardo et al. Base-controlled regioselective functionalization of chloro-substituted quinolines. The Journal of Organic Chemistry, v. 83, n. 2, p. 871-880, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.7b02855. Acesso em: 23 jul. 2024.
APA
Murie, V. E., Nishimura, R. H. V., Rolim, L. A., Vessecchi, R., Lopes, N. P., & Clososki, G. C. (2018). Base-controlled regioselective functionalization of chloro-substituted quinolines. The Journal of Organic Chemistry, 83( 2), 871-880. doi:10.1021/acs.joc.7b02855
NLM
Murie VE, Nishimura RHV, Rolim LA, Vessecchi R, Lopes NP, Clososki GC. Base-controlled regioselective functionalization of chloro-substituted quinolines [Internet]. The Journal of Organic Chemistry. 2018 ; 83( 2): 871-880.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1021/acs.joc.7b02855
Vancouver
Murie VE, Nishimura RHV, Rolim LA, Vessecchi R, Lopes NP, Clososki GC. Base-controlled regioselective functionalization of chloro-substituted quinolines [Internet]. The Journal of Organic Chemistry. 2018 ; 83( 2): 871-880.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1021/acs.joc.7b02855
Artigo de periodico
Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl (2017)
Bozzini, Leandro A; Batista, João H. C.; Mello, Murilo B. M. de; Vessecchi, Ricardo; Clososki, Giuliano Cesar
Fonte: Tetrahedron Letters. Unidades: FFCLRP, FCFRP
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
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ABNT
BOZZINI, Leandro A et al. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, v. 58, p. 4186-4190, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.09.051. Acesso em: 23 jul. 2024.
APA
Bozzini, L. A., Batista, J. H. C., Mello, M. B. M. de, Vessecchi, R., & Clososki, G. C. (2017). Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, 58, 4186-4190. doi:10.1016/j.tetlet.2017.09.051
NLM
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Vancouver
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Artigo de periodico
Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism (2017)
Paludo, Camila Raquel; Silva-Junior, Eduardo Afonso da; Silva, Eliane de Oliveira; Vessecchi, Ricardo; Lopes, Norberto Peporine; Pupo, Mônica Tallarico; Emery, Flavio da Silva; Gonçalves, Natália dos Santos; Santos, Raquel Alves dos; Furtado, Niege Araçari Jacometti Cardoso
Fonte: European Journal of Drug Metabolism and Pharmacokinetics. Unidade: FCFRP
Assuntos: CITOTOXINAS, METABOLISMO, SANGUE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALUDO, Camila Raquel et al. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism. European Journal of Drug Metabolism and Pharmacokinetics, v. 42, n. 2, p. 213-220, 2017Tradução . . Disponível em: https://doi.org/10.1007/s13318-016-0337-2. Acesso em: 23 jul. 2024.
APA
Paludo, C. R., Silva-Junior, E. A. da, Silva, E. de O., Vessecchi, R., Lopes, N. P., Pupo, M. T., et al. (2017). Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism. European Journal of Drug Metabolism and Pharmacokinetics, 42( 2), 213-220. doi:10.1007/s13318-016-0337-2
NLM
Paludo CR, Silva-Junior EA da, Silva E de O, Vessecchi R, Lopes NP, Pupo MT, Emery F da S, Gonçalves N dos S, Santos RA dos, Furtado NAJC. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2017 ; 42( 2): 213-220.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1007/s13318-016-0337-2
Vancouver
Paludo CR, Silva-Junior EA da, Silva E de O, Vessecchi R, Lopes NP, Pupo MT, Emery F da S, Gonçalves N dos S, Santos RA dos, Furtado NAJC. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2017 ; 42( 2): 213-220.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1007/s13318-016-0337-2
Artigo de periodico
Gas-phase dissociation study of erythrinian alkaloids by electrospray ionization mass spectrometry and computational methods (2017)
Guaratini, Thais; Feitosa, Luís Guilherme Pereira; Silva, Denise Brentan da; Lopes, Norberto Peporine; Lopes, João Luis Callegari; Vessecchi, Ricardo
Fonte: Journal of Mass Spectrometry. Unidades: FCFRP, FFCLRP
Assuntos: PRODUTOS NATURAIS, ALCALOIDES, ESPECTROMETRIA DE MASSAS, MONÓXIDO DE CARBONO
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ABNT
GUARATINI, Thais et al. Gas-phase dissociation study of erythrinian alkaloids by electrospray ionization mass spectrometry and computational methods. Journal of Mass Spectrometry, v. 52, n. 9, p. 571-579, 2017Tradução . . Disponível em: https://doi.org/10.1002/jms.3962. Acesso em: 23 jul. 2024.
APA
Guaratini, T., Feitosa, L. G. P., Silva, D. B. da, Lopes, N. P., Lopes, J. L. C., & Vessecchi, R. (2017). Gas-phase dissociation study of erythrinian alkaloids by electrospray ionization mass spectrometry and computational methods. Journal of Mass Spectrometry, 52( 9), 571-579. doi:10.1002/jms.3962
NLM
Guaratini T, Feitosa LGP, Silva DB da, Lopes NP, Lopes JLC, Vessecchi R. Gas-phase dissociation study of erythrinian alkaloids by electrospray ionization mass spectrometry and computational methods [Internet]. Journal of Mass Spectrometry. 2017 ; 52( 9): 571-579.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.3962
Vancouver
Guaratini T, Feitosa LGP, Silva DB da, Lopes NP, Lopes JLC, Vessecchi R. Gas-phase dissociation study of erythrinian alkaloids by electrospray ionization mass spectrometry and computational methods [Internet]. Journal of Mass Spectrometry. 2017 ; 52( 9): 571-579.[citado 2024 jul. 23 ] Available from: https://doi.org/10.1002/jms.3962

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