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  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: COMBUSTÍVEIS, DIÓXIDO DE CARBONO, COMPOSTOS ORGÂNICOS, FLUORESCÊNCIA

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      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://dx.doi.org/10.1021/acs.joc.1c00929. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: https://dx.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 2022 nov. 28 ] Available from: https://dx.doi.org/10.1021/acs.joc.1c00929
  • Source: Journal of Organic Chemistry. Unidade: IQSC

    Subject: QUÍMICA ORGÂNICA

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      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: http://dx.doi.org/10.1021/acs.joc.6b02472. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.6b02472
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: SOLVENTE, CATÁLISE, REAÇÕES QUÍMICAS

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      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: http://dx.doi.org/10.1021/acs.joc.5b02846. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.5b02846
  • Source: Journal of Organic Chemistry. Unidade: IQSC

    Subject: SÍNTESE ORGÂNICA

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      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: http://dx.doi.org/10.1021/acs.joc.6b01575. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.6b01575
  • Source: Journal of Organic Chemistry. Unidade: IFSC

    Subjects: QUÍMICA MÉDICA, PRODUTOS NATURAIS, PLANTAS MEDICINAIS

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      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: http://dx.doi.org/10.1021/acs.joc.6b01270. Acesso em: 28 nov. 2022.
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      Santos, M. S., Ruiz, A. L. T. G., Vendramini-Costa, D. B., Fernandes, D. C., Rodrigues Jr., M. T., Regiani, T., 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, Ruiz ALTG, Vendramini-Costa DB, Fernandes DC, Rodrigues Jr. MT, Regiani T, Andricopulo AD, 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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.6b01270
    • Vancouver

      Santos MS, Ruiz ALTG, Vendramini-Costa DB, Fernandes DC, Rodrigues Jr. MT, Regiani T, Andricopulo AD, 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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.6b01270
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: METAIS, IODO

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      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: http://dx.doi.org/10.1021/acs.joc.5b02803. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.5b02803
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: BIOLUMINESCÊNCIA, QUÍMICA ORGÂNICA

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      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: http://dx.doi.org/10.1021/acs.joc.5b00515. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.5b00515
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: DENSIDADE, QUÍMICA COLOIDAL

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      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: http://dx.doi.org/10.1021/acs.joc.5b01289. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.5b01289
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subject: FOTOQUÍMICA

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      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: http://dx.doi.org/10.1021/acs.joc.5b00633. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/acs.joc.5b00633
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: SOLVENTE, QUÍMICA ORGÂNICA

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      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: http://dx.doi.org/10.1021/jo400426y. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo400426y
  • Source: Journal of Organic Chemistry. Unidade: FFCLRP

    Subjects: QUÍMICA ORGÂNICA, SOLVENTE, PRODUTOS NATURAIS

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      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: http://dx.doi.org/10.1021/jo301595b. Acesso em: 28 nov. 2022.
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      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. Recuperado de http://dx.doi.org/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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo301595b
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subject: LUMINESCÊNCIA

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      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: http://dx.doi.org/10.1021/jo301309v. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo301309v
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: ESTEREOQUÍMICA, QUÍMICA ORGÂNICA

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      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: http://dx.doi.org/10.1021/jo1025089. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo1025089
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: ÁCIDOS CARBOXÍLICOS, QUÍMICA ORGÂNICA

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      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: http://dx.doi.org/10.1021/jo102413u. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo102413u
  • Source: Journal of Organic Chemistry. Unidades: IQ, FFCLRP

    Subject: TERAPIA FOTODINÂMICA

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      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: http://dx.doi.org/10.1021/jo201568n. Acesso em: 28 nov. 2022.
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      Uchoa, A. F., Iamamoto, Y., Serra, O. A., Oliveira, K. T. de, Baptista, M. da S., & Bortoluzzi, A. J. (2011). Chlorin photosensitizers sterically designed to prevent self-aggregation. Journal of Organic Chemistry, 76( 21), 8824-8832. doi:10.1021/jo201568n
    • NLM

      Uchoa AF, Iamamoto Y, Serra OA, Oliveira KT de, Baptista M da S, Bortoluzzi AJ. Chlorin photosensitizers sterically designed to prevent self-aggregation [Internet]. Journal of Organic Chemistry. 2011 ; 76( 21): 8824-8832.[citado 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo201568n
    • Vancouver

      Uchoa AF, Iamamoto Y, Serra OA, Oliveira KT de, Baptista M da S, Bortoluzzi AJ. Chlorin photosensitizers sterically designed to prevent self-aggregation [Internet]. Journal of Organic Chemistry. 2011 ; 76( 21): 8824-8832.[citado 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo201568n
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA

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      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: http://dx.doi.org/10.1021/jo101227j. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo101227j
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, SESQUITERPENOS

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      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: 28 nov. 2022.
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      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 2022 nov. 28 ] 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 2022 nov. 28 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo100108b
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: LUMINESCÊNCIA, QUÍMICA ORGÂNICA

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      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: http://dx.doi.org/10.1021/jo1013405. Acesso em: 28 nov. 2022.
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      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 2022 nov. 28 ] Available from: http://dx.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 2022 nov. 28 ] Available from: http://dx.doi.org/10.1021/jo1013405
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, PRODUTOS NATURAIS

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      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: 28 nov. 2022.
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      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
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      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 2022 nov. 28 ] 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 2022 nov. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subject: FOTOQUÍMICA

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      CISCATO, Luiz Francisco Monteiro Leite et al. Direct kinetic observation of the chemiexcitation step in peroxyoxalate chemiluminescence. Journal of Organic Chemistry, v. 74, n. 23, p. 8974-8979, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/jo901402k. Acesso em: 28 nov. 2022.
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      Ciscato, L. F. M. L., Bartoloni, F. H., Bastos, E. L., & Baader, W. J. (2009). Direct kinetic observation of the chemiexcitation step in peroxyoxalate chemiluminescence. Journal of Organic Chemistry, 74( 23), 8974-8979. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/jo901402k
    • NLM

      Ciscato LFML, Bartoloni FH, Bastos EL, Baader WJ. Direct kinetic observation of the chemiexcitation step in peroxyoxalate chemiluminescence [Internet]. Journal of Organic Chemistry. 2009 ; 74( 23): 8974-8979.[citado 2022 nov. 28 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo901402k
    • Vancouver

      Ciscato LFML, Bartoloni FH, Bastos EL, Baader WJ. Direct kinetic observation of the chemiexcitation step in peroxyoxalate chemiluminescence [Internet]. Journal of Organic Chemistry. 2009 ; 74( 23): 8974-8979.[citado 2022 nov. 28 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo901402k

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