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Artigo de periodico
Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation (2023)
Moreira, Natália Menezes; Miranda, Ingrid Telles de; Santos, Jhonathan Renner Nunes dos ; Opatz, Till ; Oliva, Glaucius ; Guido, Rafael Victorio Carvalho ; Corrêa, Arlene Gonçalves
Source: Journal of Organic Chemistry. Unidade: IFSC
Subjects: COBRE, CATALISADORES, COMPOSTOS ORGÂNICOS, SOLVENTE
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ABNT
MOREIRA, Natália Menezes et al. Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation. Journal of Organic Chemistry, v. 88, n. 13, p. 8781-8790 + supporting information: 1-30, 2023Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.3c00616. Acesso em: 27 abr. 2024.
APA
Moreira, N. M., Miranda, I. T. de, Santos, J. R. N. dos, Opatz, T., Oliva, G., Guido, R. V. C., & Corrêa, A. G. (2023). Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation. Journal of Organic Chemistry, 88( 13), 8781-8790 + supporting information: 1-30. doi:10.1021/acs.joc.3c00616
NLM
Moreira NM, Miranda IT de, Santos JRN dos, Opatz T, Oliva G, Guido RVC, Corrêa AG. Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation [Internet]. Journal of Organic Chemistry. 2023 ; 88( 13): 8781-8790 + supporting information: 1-30.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.3c00616
Vancouver
Moreira NM, Miranda IT de, Santos JRN dos, Opatz T, Oliva G, Guido RVC, Corrêa AG. Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation [Internet]. Journal of Organic Chemistry. 2023 ; 88( 13): 8781-8790 + supporting information: 1-30.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.3c00616
Artigo de periodico
Cyclic peroxidic carbon dioxide dimer fuels peroxyoxalate chemiluminescence (2021)
Silva, Sandra M. da; Lang, André Passaretti; Santos, Ana Paula Fileno dos; Cabello, Maidileyvis Castro; Ciscato, Luiz Francisco Monteiro Leite ; Bartoloni, Fernando Heering ; Bastos, Erick Leite ; Baader, Wilhelm Josef
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: COMBUSTÍVEIS, DIÓXIDO DE CARBONO, COMPOSTOS ORGÂNICOS, FLUORESCÊNCIA
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ABNT
SILVA, Sandra M. da et al. Cyclic peroxidic carbon dioxide dimer fuels peroxyoxalate chemiluminescence. Journal of Organic Chemistry, v. 86, n. 17, p. 11434–11441, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.1c00929. Acesso em: 27 abr. 2024.
APA
Silva, S. M. da, Lang, A. P., Santos, A. P. F. dos, Cabello, M. C., Ciscato, L. F. M. L., Bartoloni, F. H., et al. (2021). Cyclic peroxidic carbon dioxide dimer fuels peroxyoxalate chemiluminescence. Journal of Organic Chemistry, 86( 17), 11434–11441. doi:10.1021/acs.joc.1c00929
NLM
Silva SM da, Lang AP, Santos APF dos, Cabello MC, Ciscato LFML, Bartoloni FH, Bastos EL, Baader WJ. Cyclic peroxidic carbon dioxide dimer fuels peroxyoxalate chemiluminescence [Internet]. Journal of Organic Chemistry. 2021 ; 86( 17): 11434–11441.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.1c00929
Vancouver
Silva SM da, Lang AP, Santos APF dos, Cabello MC, Ciscato LFML, Bartoloni FH, Bastos EL, Baader WJ. Cyclic peroxidic carbon dioxide dimer fuels peroxyoxalate chemiluminescence [Internet]. Journal of Organic Chemistry. 2021 ; 86( 17): 11434–11441.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.1c00929
Artigo de periodico
Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform (2017)
Nagymihaly, Zoltan; Caturello, Naidel A. M. S.; Takatsy, Aniko; Aragay, Gemm; Kollar, Laszlo; Albuquerque, Rodrigo Queiroz de; Csok, Zsolt
Source: Journal of Organic Chemistry. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
NAGYMIHALY, Zoltan et al. Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform. Journal of Organic Chemistry, v. 82, n. 1, 2017Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b02472. Acesso em: 27 abr. 2024.
APA
Nagymihaly, Z., Caturello, N. A. M. S., Takatsy, A., Aragay, G., Kollar, L., Albuquerque, R. Q. de, & Csok, Z. (2017). Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform. Journal of Organic Chemistry, 82( 1). doi:10.1021/acs.joc.6b02472
NLM
Nagymihaly Z, Caturello NAMS, Takatsy A, Aragay G, Kollar L, Albuquerque RQ de, Csok Z. Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform [Internet]. Journal of Organic Chemistry. 2017 ; 82( 1):[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.6b02472
Vancouver
Nagymihaly Z, Caturello NAMS, Takatsy A, Aragay G, Kollar L, Albuquerque RQ de, Csok Z. Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform [Internet]. Journal of Organic Chemistry. 2017 ; 82( 1):[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.6b02472
Artigo de periodico
Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds (2016)
Silva, Juliana de Oliveira; Angnes, Ricardo A; Silva, Vitor Hugo Menezes da; Servilha, Bruno M; Adeel, Muhammad; Braga, Ataualpa Albert Carmo ; Aponick, Aaron; Correia, Carlos Roque Duarte
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: SOLVENTE, CATÁLISE, REAÇÕES QUÍMICAS
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ABNT
SILVA, Juliana de Oliveira et al. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, v. 81, n. 5, p. 2010-2018, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b02846. Acesso em: 27 abr. 2024.
APA
Silva, J. de O., Angnes, R. A., Silva, V. H. M. da, Servilha, B. M., Adeel, M., Braga, A. A. C., et al. (2016). Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, 81( 5), 2010-2018. doi:10.1021/acs.joc.5b02846
NLM
Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b02846
Vancouver
Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b02846
Artigo de periodico
Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal (2016)
Kawamura, Meire Yasuko; Talero, Alexánder G; Santiago, João V; Garambel-Vilca, Edson; Rosset, Isac G; Burtoloso, Antonio Carlos Bender
Source: Journal of Organic Chemistry. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
KAWAMURA, Meire Yasuko et al. Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal. Journal of Organic Chemistry, v. 81, n. 21, p. 10569-10575, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b01575. Acesso em: 27 abr. 2024.
APA
Kawamura, M. Y., Talero, A. G., Santiago, J. V., Garambel-Vilca, E., Rosset, I. G., & Burtoloso, A. C. B. (2016). Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal. Journal of Organic Chemistry, 81( 21), 10569-10575. doi:10.1021/acs.joc.6b01575
NLM
Kawamura MY, Talero AG, Santiago JV, Garambel-Vilca E, Rosset IG, Burtoloso ACB. Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal [Internet]. Journal of Organic Chemistry. 2016 ; 81( 21): 10569-10575.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.6b01575
Vancouver
Kawamura MY, Talero AG, Santiago JV, Garambel-Vilca E, Rosset IG, Burtoloso ACB. Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal [Internet]. Journal of Organic Chemistry. 2016 ; 81( 21): 10569-10575.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.6b01575
Artigo de periodico
Diastereoselective synthesis of biologically active cyclopenta[b]indoles (2016)
Santos, Marilia S.; Fernandes, Daniara C.; Rodrigues Jr., Manoel T.; Regiani, Thais; Andricopulo, Adriano Defini; Ruiz, Ana Lúcia T. G.; Vendramini-Costa, Débora B.; Carvalho, João E. de; Eberlin, Marcos N.; Coelho, Fernando
Source: Journal of Organic Chemistry. Unidade: IFSC
Subjects: QUÍMICA MÉDICA, PRODUTOS NATURAIS, PLANTAS MEDICINAIS
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ABNT
SANTOS, Marilia S. et al. Diastereoselective synthesis of biologically active cyclopenta[b]indoles. Journal of Organic Chemistry, v. 81, n. 15, p. 6626-6639, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b01270. Acesso em: 27 abr. 2024.
APA
Santos, M. S., Fernandes, D. C., Rodrigues Jr., M. T., Regiani, T., Andricopulo, A. D., Ruiz, A. L. T. G., et al. (2016). Diastereoselective synthesis of biologically active cyclopenta[b]indoles. Journal of Organic Chemistry, 81( 15), 6626-6639. doi:10.1021/acs.joc.6b01270
NLM
Santos MS, Fernandes DC, Rodrigues Jr. MT, Regiani T, Andricopulo AD, Ruiz ALTG, Vendramini-Costa DB, Carvalho JE de, Eberlin MN, Coelho F. Diastereoselective synthesis of biologically active cyclopenta[b]indoles [Internet]. Journal of Organic Chemistry. 2016 ; 81( 15): 6626-6639.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.6b01270
Vancouver
Santos MS, Fernandes DC, Rodrigues Jr. MT, Regiani T, Andricopulo AD, Ruiz ALTG, Vendramini-Costa DB, Carvalho JE de, Eberlin MN, Coelho F. Diastereoselective synthesis of biologically active cyclopenta[b]indoles [Internet]. Journal of Organic Chemistry. 2016 ; 81( 15): 6626-6639.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.6b01270
Artigo de periodico
Metal-Free asymmetric synthesis of indanes through chiral hypervalent iodine(III)-mediated ring contraction (2016)
Ahmad, Anees; Silva Junior, Luiz Fernando da
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: METAIS, IODO
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ABNT
AHMAD, Anees e SILVA JUNIOR, Luiz Fernando da. Metal-Free asymmetric synthesis of indanes through chiral hypervalent iodine(III)-mediated ring contraction. Journal of Organic Chemistry, v. 81, p. 2174−2181, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b02803. Acesso em: 27 abr. 2024.
APA
Ahmad, A., & Silva Junior, L. F. da. (2016). Metal-Free asymmetric synthesis of indanes through chiral hypervalent iodine(III)-mediated ring contraction. Journal of Organic Chemistry, 81, 2174−2181. doi:10.1021/acs.joc.5b02803
NLM
Ahmad A, Silva Junior LF da. Metal-Free asymmetric synthesis of indanes through chiral hypervalent iodine(III)-mediated ring contraction [Internet]. Journal of Organic Chemistry. 2016 ; 81 2174−2181.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b02803
Vancouver
Ahmad A, Silva Junior LF da. Metal-Free asymmetric synthesis of indanes through chiral hypervalent iodine(III)-mediated ring contraction [Internet]. Journal of Organic Chemistry. 2016 ; 81 2174−2181.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b02803
Artigo de periodico
Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects (2015)
Bartoloni, Fernando Heering; Oliveira, Marcelo Almeida de; Ciscato, Luiz Francisco Monteiro Leite; Augusto, Felipe Alberto; Bastos, Erick Leite ; Baader, Wilhelm Josef
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: BIOLUMINESCÊNCIA, QUÍMICA ORGÂNICA
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ABNT
BARTOLONI, Fernando Heering et al. Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects. Journal of Organic Chemistry, v. 80, n. 8, p. 3745-3751, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b00515. Acesso em: 27 abr. 2024.
APA
Bartoloni, F. H., Oliveira, M. A. de, Ciscato, L. F. M. L., Augusto, F. A., Bastos, E. L., & Baader, W. J. (2015). Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects. Journal of Organic Chemistry, 80( 8), 3745-3751. doi:10.1021/acs.joc.5b00515
NLM
Bartoloni FH, Oliveira MA de, Ciscato LFML, Augusto FA, Bastos EL, Baader WJ. Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects [Internet]. Journal of Organic Chemistry. 2015 ; 80( 8): 3745-3751.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b00515
Vancouver
Bartoloni FH, Oliveira MA de, Ciscato LFML, Augusto FA, Bastos EL, Baader WJ. Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects [Internet]. Journal of Organic Chemistry. 2015 ; 80( 8): 3745-3751.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b00515
Artigo de periodico
Molecular dynamics simulations of the initial-state predict product distributions of dediazoniation of aryldiazonium in binary solvents (2015)
Cruz, Gustavo Novaes da; Lima, Filipe da Silva; Dias, Luís Gustavo; El Seoud, Omar A ; Horinek, Dominik; Chaimovich Guralnik, Hernan ; Cuccovia, Iolanda Midea
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: DENSIDADE, QUÍMICA COLOIDAL
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ABNT
CRUZ, Gustavo Novaes da et al. Molecular dynamics simulations of the initial-state predict product distributions of dediazoniation of aryldiazonium in binary solvents. Journal of Organic Chemistry, v. 80, n. 17, p. 8637-8642, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b01289. Acesso em: 27 abr. 2024.
APA
Cruz, G. N. da, Lima, F. da S., Dias, L. G., El Seoud, O. A., Horinek, D., Chaimovich Guralnik, H., & Cuccovia, I. M. (2015). Molecular dynamics simulations of the initial-state predict product distributions of dediazoniation of aryldiazonium in binary solvents. Journal of Organic Chemistry, 80( 17), 8637-8642. doi:10.1021/acs.joc.5b01289
NLM
Cruz GN da, Lima F da S, Dias LG, El Seoud OA, Horinek D, Chaimovich Guralnik H, Cuccovia IM. Molecular dynamics simulations of the initial-state predict product distributions of dediazoniation of aryldiazonium in binary solvents [Internet]. Journal of Organic Chemistry. 2015 ; 80( 17): 8637-8642.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b01289
Vancouver
Cruz GN da, Lima F da S, Dias LG, El Seoud OA, Horinek D, Chaimovich Guralnik H, Cuccovia IM. Molecular dynamics simulations of the initial-state predict product distributions of dediazoniation of aryldiazonium in binary solvents [Internet]. Journal of Organic Chemistry. 2015 ; 80( 17): 8637-8642.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b01289
Artigo de periodico
Mechanism of photochemical O-atom exchange in nitrosamines with molecular oxygen (2015)
Oliveira, Marilene Silva; Ghogare, Ashwini A; Abramova, Inna; Greer, Edyta M; Prado, Fernanda Manso ; Di Mascio, Paolo ; Greer, Alexander
Source: Journal of Organic Chemistry. Unidade: IQ
Assunto: FOTOQUÍMICA
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ABNT
OLIVEIRA, Marilene Silva et al. Mechanism of photochemical O-atom exchange in nitrosamines with molecular oxygen. Journal of Organic Chemistry, v. 80, n. 12, p. 6119-6127, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b00633. Acesso em: 27 abr. 2024.
APA
Oliveira, M. S., Ghogare, A. A., Abramova, I., Greer, E. M., Prado, F. M., Di Mascio, P., & Greer, A. (2015). Mechanism of photochemical O-atom exchange in nitrosamines with molecular oxygen. Journal of Organic Chemistry, 80( 12), 6119-6127. doi:10.1021/acs.joc.5b00633
NLM
Oliveira MS, Ghogare AA, Abramova I, Greer EM, Prado FM, Di Mascio P, Greer A. Mechanism of photochemical O-atom exchange in nitrosamines with molecular oxygen [Internet]. Journal of Organic Chemistry. 2015 ; 80( 12): 6119-6127.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b00633
Vancouver
Oliveira MS, Ghogare AA, Abramova I, Greer EM, Prado FM, Di Mascio P, Greer A. Mechanism of photochemical O-atom exchange in nitrosamines with molecular oxygen [Internet]. Journal of Organic Chemistry. 2015 ; 80( 12): 6119-6127.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/acs.joc.5b00633
Artigo de periodico
Solvent cage effects: basis of a general mechanism for efficient chemiluminescence (2013)
Bastos, Erick Leite ; Silva, Sandra Maria da; Baader, Wilhelm Josef
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: SOLVENTE, QUÍMICA ORGÂNICA
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ABNT
BASTOS, Erick Leite e SILVA, Sandra Maria da e BAADER, Wilhelm Josef. Solvent cage effects: basis of a general mechanism for efficient chemiluminescence. Journal of Organic Chemistry, v. 78, n. 9, p. 4432-4439, 2013Tradução . . Disponível em: https://doi.org/10.1021/jo400426y. Acesso em: 27 abr. 2024.
APA
Bastos, E. L., Silva, S. M. da, & Baader, W. J. (2013). Solvent cage effects: basis of a general mechanism for efficient chemiluminescence. Journal of Organic Chemistry, 78( 9), 4432-4439. doi:10.1021/jo400426y
NLM
Bastos EL, Silva SM da, Baader WJ. Solvent cage effects: basis of a general mechanism for efficient chemiluminescence [Internet]. Journal of Organic Chemistry. 2013 ; 78( 9): 4432-4439.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo400426y
Vancouver
Bastos EL, Silva SM da, Baader WJ. Solvent cage effects: basis of a general mechanism for efficient chemiluminescence [Internet]. Journal of Organic Chemistry. 2013 ; 78( 9): 4432-4439.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo400426y
Artigo de periodico
Solvent effect in reactions using Stryker's reagent (2012)
Sass, Daiane Cristina; Heleno, Vladimir Constantino Gomes; Cavalcante, Simone; Barbosa, Jader da Silva; Soares, Ana Carolina Ferreira; Constantino, Maurício Gomes
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Subjects: QUÍMICA ORGÂNICA, SOLVENTE, PRODUTOS NATURAIS
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ABNT
SASS, Daiane Cristina et al. Solvent effect in reactions using Stryker's reagent. Journal of Organic Chemistry, v. 77, n. 20, p. 9374-9378, 2012Tradução . . Disponível em: https://doi.org/10.1021/jo301595b. Acesso em: 27 abr. 2024.
APA
Sass, D. C., Heleno, V. C. G., Cavalcante, S., Barbosa, J. da S., Soares, A. C. F., & Constantino, M. G. (2012). Solvent effect in reactions using Stryker's reagent. Journal of Organic Chemistry, 77( 20), 9374-9378. doi:10.1021/jo301595b
NLM
Sass DC, Heleno VCG, Cavalcante S, Barbosa J da S, Soares ACF, Constantino MG. Solvent effect in reactions using Stryker's reagent [Internet]. Journal of Organic Chemistry. 2012 ; 77( 20): 9374-9378.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo301595b
Vancouver
Sass DC, Heleno VCG, Cavalcante S, Barbosa J da S, Soares ACF, Constantino MG. Solvent effect in reactions using Stryker's reagent [Internet]. Journal of Organic Chemistry. 2012 ; 77( 20): 9374-9378.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo301595b
Artigo de periodico
Revision of singlet quantum yields in the catalyzed decomposition of cyclic peroxides (2012)
Oliveira, Marcelo Almeida de; Bartoloni, Fernando Heering; Augusto, Felipe Alberto; Ciscato, Luiz Francisco Monteiro Leite; Bastos, Erick Leite ; Baader, Wilhelm Josef
Source: Journal of Organic Chemistry. Unidade: IQ
Assunto: LUMINESCÊNCIA
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ABNT
OLIVEIRA, Marcelo Almeida de et al. Revision of singlet quantum yields in the catalyzed decomposition of cyclic peroxides. Journal of Organic Chemistry, v. 77, n. 23, p. 10537-10544, 2012Tradução . . Disponível em: https://doi.org/10.1021/jo301309v. Acesso em: 27 abr. 2024.
APA
Oliveira, M. A. de, Bartoloni, F. H., Augusto, F. A., Ciscato, L. F. M. L., Bastos, E. L., & Baader, W. J. (2012). Revision of singlet quantum yields in the catalyzed decomposition of cyclic peroxides. Journal of Organic Chemistry, 77( 23), 10537-10544. doi:10.1021/jo301309v
NLM
Oliveira MA de, Bartoloni FH, Augusto FA, Ciscato LFML, Bastos EL, Baader WJ. Revision of singlet quantum yields in the catalyzed decomposition of cyclic peroxides [Internet]. Journal of Organic Chemistry. 2012 ; 77( 23): 10537-10544.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo301309v
Vancouver
Oliveira MA de, Bartoloni FH, Augusto FA, Ciscato LFML, Bastos EL, Baader WJ. Revision of singlet quantum yields in the catalyzed decomposition of cyclic peroxides [Internet]. Journal of Organic Chemistry. 2012 ; 77( 23): 10537-10544.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo301309v
Artigo de periodico
Structure elucidation and absolute stereochemistry of isomeric monoterpene chromane esters (2011)
Batista Jr., João Marcos; Batista, Andrea N. L; Mota, Jonas da Silva; Cass, Quezia Bezerra; Kato, Massuo Jorge ; Bolzani, Vanderlan da Silva; Freedman, Teresa B; López, Silvia Noelí; Furlan, Maysa; Nafie, Laurence A
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: ESTEREOQUÍMICA, QUÍMICA ORGÂNICA
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ABNT
BATISTA JR., João Marcos et al. Structure elucidation and absolute stereochemistry of isomeric monoterpene chromane esters. Journal of Organic Chemistry, v. 76, n. 8, p. 2603-2612, 2011Tradução . . Disponível em: https://doi.org/10.1021/jo1025089. Acesso em: 27 abr. 2024.
APA
Batista Jr., J. M., Batista, A. N. L., Mota, J. da S., Cass, Q. B., Kato, M. J., Bolzani, V. da S., et al. (2011). Structure elucidation and absolute stereochemistry of isomeric monoterpene chromane esters. Journal of Organic Chemistry, 76( 8), 2603-2612. doi:10.1021/jo1025089
NLM
Batista Jr. JM, Batista ANL, Mota J da S, Cass QB, Kato MJ, Bolzani V da S, Freedman TB, López SN, Furlan M, Nafie LA. Structure elucidation and absolute stereochemistry of isomeric monoterpene chromane esters [Internet]. Journal of Organic Chemistry. 2011 ; 76( 8): 2603-2612.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo1025089
Vancouver
Batista Jr. JM, Batista ANL, Mota J da S, Cass QB, Kato MJ, Bolzani V da S, Freedman TB, López SN, Furlan M, Nafie LA. Structure elucidation and absolute stereochemistry of isomeric monoterpene chromane esters [Internet]. Journal of Organic Chemistry. 2011 ; 76( 8): 2603-2612.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo1025089
Artigo de periodico
Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III) (2011)
Vasconcelos, Ramon Sonedson; Silva Junior, Luiz Fernando da; Giannis, Athanassios
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: ÁCIDOS CARBOXÍLICOS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Ramon Sonedson e SILVA JUNIOR, Luiz Fernando da e GIANNIS, Athanassios. Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III). Journal of Organic Chemistry, v. 76, n. 5, p. 1499-1502, 2011Tradução . . Disponível em: https://doi.org/10.1021/jo102413u. Acesso em: 27 abr. 2024.
APA
Vasconcelos, R. S., Silva Junior, L. F. da, & Giannis, A. (2011). Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III). Journal of Organic Chemistry, 76( 5), 1499-1502. doi:10.1021/jo102413u
NLM
Vasconcelos RS, Silva Junior LF da, Giannis A. Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III) [Internet]. Journal of Organic Chemistry. 2011 ; 76( 5): 1499-1502.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo102413u
Vancouver
Vasconcelos RS, Silva Junior LF da, Giannis A. Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III) [Internet]. Journal of Organic Chemistry. 2011 ; 76( 5): 1499-1502.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo102413u
Artigo de periodico
Chlorin photosensitizers sterically designed to prevent self-aggregation (2011)
Uchoa, Adjaci Fernandes; Oliveira, Kleber Thiago de; Baptista, Maurício da Silva ; Bortoluzzi, Adailton J; Iamamoto, Yassuko; Serra, Osvaldo Antonio
Source: Journal of Organic Chemistry. Unidades: IQ, FFCLRP
Assunto: TERAPIA FOTODINÂMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
UCHOA, Adjaci Fernandes et al. Chlorin photosensitizers sterically designed to prevent self-aggregation. Journal of Organic Chemistry, v. 76, n. 21, p. 8824-8832, 2011Tradução . . Disponível em: https://doi.org/10.1021/jo201568n. Acesso em: 27 abr. 2024.
APA
Uchoa, A. F., Oliveira, K. T. de, Baptista, M. da S., Bortoluzzi, A. J., Iamamoto, Y., & Serra, O. A. (2011). Chlorin photosensitizers sterically designed to prevent self-aggregation. Journal of Organic Chemistry, 76( 21), 8824-8832. doi:10.1021/jo201568n
NLM
Uchoa AF, Oliveira KT de, Baptista M da S, Bortoluzzi AJ, Iamamoto Y, Serra OA. Chlorin photosensitizers sterically designed to prevent self-aggregation [Internet]. Journal of Organic Chemistry. 2011 ; 76( 21): 8824-8832.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo201568n
Vancouver
Uchoa AF, Oliveira KT de, Baptista M da S, Bortoluzzi AJ, Iamamoto Y, Serra OA. Chlorin photosensitizers sterically designed to prevent self-aggregation [Internet]. Journal of Organic Chemistry. 2011 ; 76( 21): 8824-8832.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo201568n
Artigo de periodico
A ring contraction strategy toward a diastereoselective total synthesis of (+)-bakkenolide A (2010)
Carneiro, Vânia Maria Teixeira; Ferraz, Helena Maria Carvalho; Vieira, Tiago de Oliveira; Ishikawa, Eloisa Erika; Silva Junior, Luiz Fernando da
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, SESQUITERPENOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARNEIRO, Vânia Maria Teixeira et al. A ring contraction strategy toward a diastereoselective total synthesis of (+)-bakkenolide A. Journal of Organic Chemistry, v. 75, n. 9, p. 2877-2882, 2010Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/jo100108b. Acesso em: 27 abr. 2024.
APA
Carneiro, V. M. T., Ferraz, H. M. C., Vieira, T. de O., Ishikawa, E. E., & Silva Junior, L. F. da. (2010). A ring contraction strategy toward a diastereoselective total synthesis of (+)-bakkenolide A. Journal of Organic Chemistry, 75( 9), 2877-2882. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/jo100108b
NLM
Carneiro VMT, Ferraz HMC, Vieira T de O, Ishikawa EE, Silva Junior LF da. A ring contraction strategy toward a diastereoselective total synthesis of (+)-bakkenolide A [Internet]. Journal of Organic Chemistry. 2010 ; 75( 9): 2877-2882.[citado 2024 abr. 27 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo100108b
Vancouver
Carneiro VMT, Ferraz HMC, Vieira T de O, Ishikawa EE, Silva Junior LF da. A ring contraction strategy toward a diastereoselective total synthesis of (+)-bakkenolide A [Internet]. Journal of Organic Chemistry. 2010 ; 75( 9): 2877-2882.[citado 2024 abr. 27 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo100108b
Artigo de periodico
Facile synthesis of koser’s reagent and derivatives from iodine or aryl iodides (2010)
Merritt, Eleanor A; Carneiro, Vânia Maria Teixeira; Silva Jr., Luiz Fernando da; Olofsson, Berit
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MERRITT, Eleanor A et al. Facile synthesis of koser’s reagent and derivatives from iodine or aryl iodides. Journal of Organic Chemistry, v. 75, n. 21, p. 7416-7419, 2010Tradução . . Disponível em: https://doi.org/10.1021/jo101227j. Acesso em: 27 abr. 2024.
APA
Merritt, E. A., Carneiro, V. M. T., Silva Jr., L. F. da, & Olofsson, B. (2010). Facile synthesis of koser’s reagent and derivatives from iodine or aryl iodides. Journal of Organic Chemistry, 75( 21), 7416-7419. doi:10.1021/jo101227j
NLM
Merritt EA, Carneiro VMT, Silva Jr. LF da, Olofsson B. Facile synthesis of koser’s reagent and derivatives from iodine or aryl iodides [Internet]. Journal of Organic Chemistry. 2010 ; 75( 21): 7416-7419.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo101227j
Vancouver
Merritt EA, Carneiro VMT, Silva Jr. LF da, Olofsson B. Facile synthesis of koser’s reagent and derivatives from iodine or aryl iodides [Internet]. Journal of Organic Chemistry. 2010 ; 75( 21): 7416-7419.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo101227j
Artigo de periodico
Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition (2010)
Ciscato, Luiz Francisco Monteiro Leite; Bartoloni, Fernando Heering; Weiss, Dieter; Beckert, Rainer; Baader, Wilhelm Josef
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: LUMINESCÊNCIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CISCATO, Luiz Francisco Monteiro Leite et al. Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition. Journal of Organic Chemistry, v. 75, n. 19, p. 6574-6580, 2010Tradução . . Disponível em: https://doi.org/10.1021/jo1013405. Acesso em: 27 abr. 2024.
APA
Ciscato, L. F. M. L., Bartoloni, F. H., Weiss, D., Beckert, R., & Baader, W. J. (2010). Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition. Journal of Organic Chemistry, 75( 19), 6574-6580. doi:10.1021/jo1013405
NLM
Ciscato LFML, Bartoloni FH, Weiss D, Beckert R, Baader WJ. Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition [Internet]. Journal of Organic Chemistry. 2010 ; 75( 19): 6574-6580.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo1013405
Vancouver
Ciscato LFML, Bartoloni FH, Weiss D, Beckert R, Baader WJ. Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition [Internet]. Journal of Organic Chemistry. 2010 ; 75( 19): 6574-6580.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1021/jo1013405
Artigo de periodico
(+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity (2009)
Bianco, Graziela Gallego; Ferraz, Helena Maria Carvalho; Costa, Arinice M.; Lotufo, Leticia Veras Costa ; Pessoa, Cláudia; Moraes, Manoel O. de; Schrems, Marcus G; Pfaltz, Andreas; Silva Jr., Luiz Fernando da
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BIANCO, Graziela Gallego et al. (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity. Journal of Organic Chemistry, v. 74, n. 6, p. 2561-2566, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jo9000405. Acesso em: 27 abr. 2024.
APA
Bianco, G. G., Ferraz, H. M. C., Costa, A. M., Lotufo, L. V. C., Pessoa, C., Moraes, M. O. de, et al. (2009). (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity. Journal of Organic Chemistry, 74( 6), 2561-2566. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jo9000405
NLM
Bianco GG, Ferraz HMC, Costa AM, Lotufo LVC, Pessoa C, Moraes MO de, Schrems MG, Pfaltz A, Silva Jr. LF da. (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity [Internet]. Journal of Organic Chemistry. 2009 ; 74( 6): 2561-2566.[citado 2024 abr. 27 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405
Vancouver
Bianco GG, Ferraz HMC, Costa AM, Lotufo LVC, Pessoa C, Moraes MO de, Schrems MG, Pfaltz A, Silva Jr. LF da. (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity [Internet]. Journal of Organic Chemistry. 2009 ; 74( 6): 2561-2566.[citado 2024 abr. 27 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405

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