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Artigo de periodico
Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman (2020)
Alves, Jacqueline Q.; Formiga, André L. B.; Gonçalves, Rogéria Rocha ; Silva, Roberto Santana da
Source: Journal of Coordination Chemistry. Unidades: FFCLRP, FCFRP
Subjects: RUTÊNIO, QUÍMICA ORGÂNICA, CATECOLAMINAS
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ABNT
ALVES, Jacqueline Q. et al. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman. Journal of Coordination Chemistry, v. 73, n. 2, p. 191-205, 2020Tradução . . Disponível em: https://doi.org/10.1080/00958972.2020.1724287. Acesso em: 16 maio 2024.
APA
Alves, J. Q., Formiga, A. L. B., Gonçalves, R. R., & Silva, R. S. da. (2020). Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman. Journal of Coordination Chemistry, 73( 2), 191-205. doi:10.1080/00958972.2020.1724287
NLM
Alves JQ, Formiga ALB, Gonçalves RR, Silva RS da. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman [Internet]. Journal of Coordination Chemistry. 2020 ; 73( 2): 191-205.[citado 2024 maio 16 ] Available from: https://doi.org/10.1080/00958972.2020.1724287
Vancouver
Alves JQ, Formiga ALB, Gonçalves RR, Silva RS da. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman [Internet]. Journal of Coordination Chemistry. 2020 ; 73( 2): 191-205.[citado 2024 maio 16 ] Available from: https://doi.org/10.1080/00958972.2020.1724287
Artigo de periodico
How does the total charge and isomerism influence the Ru–NO ammine complexes? (2018)
Orenha, Renato Pereira ; Tfouni, Elia ; Galembeck, Sérgio Emanuel
Source: Physical Chemistry Chemical Physics. Unidade: FFCLRP
Subjects: QUÍMICA ORGÂNICA, RUTÊNIO, ÓXIDO NÍTRICO
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ABNT
ORENHA, Renato Pereira e TFOUNI, Elia e GALEMBECK, Sérgio Emanuel. How does the total charge and isomerism influence the Ru–NO ammine complexes?. Physical Chemistry Chemical Physics, v. 20, n. 19, p. 13348-13356, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8cp00865e. Acesso em: 16 maio 2024.
APA
Orenha, R. P., Tfouni, E., & Galembeck, S. E. (2018). How does the total charge and isomerism influence the Ru–NO ammine complexes? Physical Chemistry Chemical Physics, 20( 19), 13348-13356. doi:10.1039/c8cp00865e
NLM
Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2024 maio 16 ] Available from: https://doi.org/10.1039/c8cp00865e
Vancouver
Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2024 maio 16 ] Available from: https://doi.org/10.1039/c8cp00865e
Artigo de periodico
Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives (2016)
Fumagalli, Fernando; Emery, Flavio da Silva
Source: The Journal of Organic Chemistry. Unidade: FCFRP
Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
FUMAGALLI, Fernando e EMERY, Flavio da Silva. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, v. 81, n. 21, p. 10339-10347, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b01329. Acesso em: 16 maio 2024.
APA
Fumagalli, F., & Emery, F. da S. (2016). Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, 81( 21), 10339-10347. doi:10.1021/acs.joc.6b01329
NLM
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2024 maio 16 ] Available from: https://doi.org/10.1021/acs.joc.6b01329
Vancouver
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2024 maio 16 ] Available from: https://doi.org/10.1021/acs.joc.6b01329
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: 16 maio 2024.
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 2024 maio 16 ] 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 2024 maio 16 ] 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: 16 maio 2024.
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 2024 maio 16 ] 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 2024 maio 16 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
Artigo de periodico
A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients (2012)
Belsito, D; Bickers, D; Bruze, M; Calow, Peter; Dagli, Maria Lúcia Zaidan; Fryer, A. D; Greim, Helmut; Miyachi, Y; Saurat, J. H; Sipes, I. G
Source: Food and Chemical Toxicology. Unidade: FMVZ
Subjects: QUÍMICA ORGÂNICA, DERMATOLOGIA, TOXICOLOGIA
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ABNT
BELSITO, D et al. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S52-S99, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.10.042. Acesso em: 16 maio 2024.
APA
Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2012). A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, 50, S52-S99. doi:10.1016/j.fct.2011.10.042
NLM
Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
Vancouver
Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
Artigo de periodico
Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis (2010)
Donnici, Claudio Luis; Pereira, Elaine Henriques Teixeira; Lopes, Júlio Cesar Dias; Marzorati, Liliana ; Wladislaw, Blanka
Source: Synthetic Communications. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
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ABNT
DONNICI, Claudio Luis et al. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications, v. 40, n. 3, p. 342-350, 2010Tradução . . Acesso em: 16 maio 2024.
APA
Donnici, C. L., Pereira, E. H. T., Lopes, J. C. D., Marzorati, L., & Wladislaw, B. (2010). Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications, 40( 3), 342-350.
NLM
Donnici CL, Pereira EHT, Lopes JCD, Marzorati L, Wladislaw B. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications. 2010 ; 40( 3): 342-350.[citado 2024 maio 16 ]
Vancouver
Donnici CL, Pereira EHT, Lopes JCD, Marzorati L, Wladislaw B. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications. 2010 ; 40( 3): 342-350.[citado 2024 maio 16 ]
Artigo de periodico
Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes (2009)
Ferraz, Helena Maria Carvalho; Carneiro, Vânia Maria Teixeira; Silva Junior, Luiz Fernando da
Source: Synthesis. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, TÁLIO, NITRATOS, CARBONO
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ABNT
FERRAZ, Helena Maria Carvalho e CARNEIRO, Vânia Maria Teixeira e SILVA JUNIOR, Luiz Fernando da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, n. 3, p. 385-388, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf. Acesso em: 16 maio 2024.
APA
Ferraz, H. M. C., Carneiro, V. M. T., & Silva Junior, L. F. da. (2009). Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, ( 3), 385-388. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
NLM
Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 maio 16 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
Vancouver
Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 maio 16 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
Artigo de periodico
Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent (2009)
Andrade, Leandro Helgueira ; Piovan, Leandro; Pasquini, Mônica D`Arcadia
Source: Tetrahedron Asymmetry. Unidade: IQ
Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA
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ABNT
ANDRADE, Leandro Helgueira e PIOVAN, Leandro e PASQUINI, Mônica D`Arcadia. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, v. 20, n. 13, p. 1521-1525, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.05.033. Acesso em: 16 maio 2024.
APA
Andrade, L. H., Piovan, L., & Pasquini, M. D. `A. (2009). Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, 20( 13), 1521-1525. doi:10.1016/j.tetasy.2009.05.033
NLM
Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
Vancouver
Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
Artigo de periodico
Application of high-resolution electrospray mass spectrometry for the elucidation of the disproportionation reaction of iodobenzene diacetate (2008)
Silva Jr., Luiz Fernando da; Vasconcelos, Ramon Sonedson; Lopes, Norberto Peporine
Source: International Journal of Mass Spectrometry. Unidades: IQ, FCFRP
Subjects: ESPECTROMETRIA DE MASSAS, QUÍMICA ORGÂNICA, ALQUILAÇÃO
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ABNT
SILVA JR., Luiz Fernando da e VASCONCELOS, Ramon Sonedson e LOPES, Norberto Peporine. Application of high-resolution electrospray mass spectrometry for the elucidation of the disproportionation reaction of iodobenzene diacetate. International Journal of Mass Spectrometry, v. 276, n. 1, p. 24-30, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.ijms.2008.06.012. Acesso em: 16 maio 2024.
APA
Silva Jr., L. F. da, Vasconcelos, R. S., & Lopes, N. P. (2008). Application of high-resolution electrospray mass spectrometry for the elucidation of the disproportionation reaction of iodobenzene diacetate. International Journal of Mass Spectrometry, 276( 1), 24-30. doi:10.1016/j.ijms.2008.06.012
NLM
Silva Jr. LF da, Vasconcelos RS, Lopes NP. Application of high-resolution electrospray mass spectrometry for the elucidation of the disproportionation reaction of iodobenzene diacetate [Internet]. International Journal of Mass Spectrometry. 2008 ; 276( 1): 24-30.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ijms.2008.06.012
Vancouver
Silva Jr. LF da, Vasconcelos RS, Lopes NP. Application of high-resolution electrospray mass spectrometry for the elucidation of the disproportionation reaction of iodobenzene diacetate [Internet]. International Journal of Mass Spectrometry. 2008 ; 276( 1): 24-30.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ijms.2008.06.012
Artigo de periodico
Uncovering false positives on a virtual screening search for cruzain inhibitors (2008)
Malvezzi, Alberto; Rezende, Leandro de; Izidoro, Mario Augusto; Cezari, Maria Helena Sedenho; Juliano, Luiz; Amaral, Antonia Tavares do
Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, PEROXIDASE
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ABNT
MALVEZZI, Alberto et al. Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, v. 18, n. 1, p. 350-354, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2007.10.068. Acesso em: 16 maio 2024.
APA
Malvezzi, A., Rezende, L. de, Izidoro, M. A., Cezari, M. H. S., Juliano, L., & Amaral, A. T. do. (2008). Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, 18( 1), 350-354. doi:10.1016/j.bmcl.2007.10.068
NLM
Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
Vancouver
Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
Artigo de periodico
Diterpenes: a therapeutic promise for cardiovascular diseases (2008)
Tirapelli, Carlos Renato; Ambrosio, Sérgio Ricardo; Costa, Fernando Batista da; Oliveira, Ana Maria de
Source: Recent Patents on Cardiovascular Drug Discovery. Unidades: EERP, FCFRP
Subjects: DOENÇAS CARDIOVASCULARES, QUÍMICA ORGÂNICA
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ABNT
TIRAPELLI, Carlos Renato et al. Diterpenes: a therapeutic promise for cardiovascular diseases. Recent Patents on Cardiovascular Drug Discovery, v. 3, n. 1, p. 1-8, 2008Tradução . . Acesso em: 16 maio 2024.
APA
Tirapelli, C. R., Ambrosio, S. R., Costa, F. B. da, & Oliveira, A. M. de. (2008). Diterpenes: a therapeutic promise for cardiovascular diseases. Recent Patents on Cardiovascular Drug Discovery, 3( 1), 1-8.
NLM
Tirapelli CR, Ambrosio SR, Costa FB da, Oliveira AM de. Diterpenes: a therapeutic promise for cardiovascular diseases. Recent Patents on Cardiovascular Drug Discovery. 2008 ; 3( 1): 1-8.[citado 2024 maio 16 ]
Vancouver
Tirapelli CR, Ambrosio SR, Costa FB da, Oliveira AM de. Diterpenes: a therapeutic promise for cardiovascular diseases. Recent Patents on Cardiovascular Drug Discovery. 2008 ; 3( 1): 1-8.[citado 2024 maio 16 ]
Artigo de periodico
Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) (2007)
Raminelli, Cristiano; Kagohara, Edna; Pellizari, Vivian Helena; Comasseto, João Valdir; Andrade, Leandro Helgueira ; Porto, Andre Luiz Meleiro
Source: Enzyme and Microbial Technology. Unidades: ICB, IQ, IQSC
Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA
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ABNT
RAMINELLI, Cristiano et al. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, v. 40, n. 2, p. 362-369, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2006.06.002. Acesso em: 16 maio 2024.
APA
Raminelli, C., Kagohara, E., Pellizari, V. H., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2007). Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, 40( 2), 362-369. doi:10.1016/j.enzmictec.2006.06.002
NLM
Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
Vancouver
Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
Artigo de periodico
Antitumor activity of extracts from Peperomia elongata (2007)
Campos, Patricia Bonavides de Castro; Gama, Juliana Julian Torres; Pereira, Lícia Pacheco; Lotufo, Leticia Veras Costa ; Moraes, Manoel Odorico de; Guimarães, Elsie Franklin; Kato, Massuo Jorge ; Furlan, Maysa; Pessoa, Claudia
Source: Pharmaceutical Biology. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS
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ABNT
CAMPOS, Patricia Bonavides de Castro et al. Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology, v. 45, n. 10, p. 760-765, 2007Tradução . . Acesso em: 16 maio 2024.
APA
Campos, P. B. de C., Gama, J. J. T., Pereira, L. P., Lotufo, L. V. C., Moraes, M. O. de, Guimarães, E. F., et al. (2007). Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology, 45( 10), 760-765.
NLM
Campos PB de C, Gama JJT, Pereira LP, Lotufo LVC, Moraes MO de, Guimarães EF, Kato MJ, Furlan M, Pessoa C. Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology. 2007 ; 45( 10): 760-765.[citado 2024 maio 16 ]
Vancouver
Campos PB de C, Gama JJT, Pereira LP, Lotufo LVC, Moraes MO de, Guimarães EF, Kato MJ, Furlan M, Pessoa C. Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology. 2007 ; 45( 10): 760-765.[citado 2024 maio 16 ]
Artigo de periodico
Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide (2007)
Valadares, Marize Campos; Rezende, Kênnia Rocha; Pereira, Enir Raquel Tavares; Sousa, Mariana Côrtes de; Gonçalves Santiago, Bruno; Assis, Juliana Cipriano de; Kato, Massuo Jorge
Source: Food and Chemical Toxicology. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
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ABNT
VALADARES, Marize Campos et al. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide. Food and Chemical Toxicology, v. 45, n. 10, p. 1975-1978, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2007.04.016. Acesso em: 16 maio 2024.
APA
Valadares, M. C., Rezende, K. R., Pereira, E. R. T., Sousa, M. C. de, Gonçalves Santiago, B., Assis, J. C. de, & Kato, M. J. (2007). Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide. Food and Chemical Toxicology, 45( 10), 1975-1978. doi:10.1016/j.fct.2007.04.016
NLM
Valadares MC, Rezende KR, Pereira ERT, Sousa MC de, Gonçalves Santiago B, Assis JC de, Kato MJ. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide [Internet]. Food and Chemical Toxicology. 2007 ; 45( 10): 1975-1978.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.fct.2007.04.016
Vancouver
Valadares MC, Rezende KR, Pereira ERT, Sousa MC de, Gonçalves Santiago B, Assis JC de, Kato MJ. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide [Internet]. Food and Chemical Toxicology. 2007 ; 45( 10): 1975-1978.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.fct.2007.04.016
Artigo de periodico
Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae) (2007)
Lopes, Adriana Aparecida; Baldoqui, Debora Cristina; López, Silvia Noelí; Kato, Massuo Jorge ; Bolzani, Vanderlan da Silva; Furlan, Maysa
Source: Phytochemistry. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Adriana Aparecida et al. Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae). Phytochemistry, v. 68, n. 15, p. 2053-2058, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2007.04.025. Acesso em: 16 maio 2024.
APA
Lopes, A. A., Baldoqui, D. C., López, S. N., Kato, M. J., Bolzani, V. da S., & Furlan, M. (2007). Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae). Phytochemistry, 68( 15), 2053-2058. doi:10.1016/j.phytochem.2007.04.025
NLM
Lopes AA, Baldoqui DC, López SN, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae) [Internet]. Phytochemistry. 2007 ; 68( 15): 2053-2058.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.phytochem.2007.04.025
Vancouver
Lopes AA, Baldoqui DC, López SN, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae) [Internet]. Phytochemistry. 2007 ; 68( 15): 2053-2058.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.phytochem.2007.04.025
Artigo de periodico
Synthetic approaches to naturally occurring ten-membered-ring lactones (2007)
Ferraz, Helena Maria Carvalho; Bombonato, Fernanda Irene; Longo Junior, Luiz Sidney
Source: Synthesis. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Helena Maria Carvalho e BOMBONATO, Fernanda Irene e LONGO JUNIOR, Luiz Sidney. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, n. 21, p. 3261-3285, 2007Tradução . . Acesso em: 16 maio 2024.
APA
Ferraz, H. M. C., Bombonato, F. I., & Longo Junior, L. S. (2007). Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, ( 21), 3261-3285.
NLM
Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 maio 16 ]
Vancouver
Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 maio 16 ]
Artigo de periodico
Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides (2006)
Dos Santos, Alcindo Aparecido; Da Costa, Carlos E.; Princival, Jefferson Luiz; Comasseto, João Valdir
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: LIPASE, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DOS SANTOS, Alcindo Aparecido et al. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, v. 17, n. 15, p. 2252-2259, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.024. Acesso em: 16 maio 2024.
APA
Dos Santos, A. A., Da Costa, C. E., Princival, J. L., & Comasseto, J. V. (2006). Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, 17( 15), 2252-2259. doi:10.1016/j.tetasy.2006.07.024
NLM
Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
Vancouver
Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
Artigo de periodico
Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton (2006)
Ferraz, Helena Maria Carvalho; Vieira, Tiago O.; Silva Jr., Luiz Fernando da
Source: Synthesis. Unidade: IQ
Subjects: TÁLIO, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Helena Maria Carvalho e VIEIRA, Tiago O. e SILVA JR., Luiz Fernando da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, n. 16, p. 2748-2752, 2006Tradução . . Acesso em: 16 maio 2024.
APA
Ferraz, H. M. C., Vieira, T. O., & Silva Jr., L. F. da. (2006). Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, ( 16), 2748-2752.
NLM
Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 maio 16 ]
Vancouver
Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 maio 16 ]
Artigo de periodico
Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae) (2006)
Kitamura, Rodrigo Ossamu Saga; Romoff, Paulete; Young, Maria Claudia Marx; Kato, Massuo Jorge ; Lago, João Henrique Ghilardi
Source: Phytochemistry. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KITAMURA, Rodrigo Ossamu Saga et al. Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae). Phytochemistry, v. 67, n. 21, p. 2398-2402, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2006.08.007. Acesso em: 16 maio 2024.
APA
Kitamura, R. O. S., Romoff, P., Young, M. C. M., Kato, M. J., & Lago, J. H. G. (2006). Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae). Phytochemistry, 67( 21), 2398-2402. doi:10.1016/j.phytochem.2006.08.007
NLM
Kitamura ROS, Romoff P, Young MCM, Kato MJ, Lago JHG. Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae) [Internet]. Phytochemistry. 2006 ; 67( 21): 2398-2402.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.phytochem.2006.08.007
Vancouver
Kitamura ROS, Romoff P, Young MCM, Kato MJ, Lago JHG. Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae) [Internet]. Phytochemistry. 2006 ; 67( 21): 2398-2402.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.phytochem.2006.08.007

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