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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://doi.org/10.1021/acs.joc.1c00929. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://doi.org/10.1021/acs.joc.1c00929
  • 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: https://doi.org/10.1021/acs.joc.5b02846. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://doi.org/10.1021/acs.joc.5b02846
  • 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: https://doi.org/10.1021/acs.joc.5b02803. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://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: https://doi.org/10.1021/acs.joc.5b00515. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://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: https://doi.org/10.1021/acs.joc.5b01289. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://doi.org/10.1021/acs.joc.5b01289
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: 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: https://doi.org/10.1021/acs.joc.5b00633. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://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: https://doi.org/10.1021/jo400426y. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://doi.org/10.1021/jo400426y
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: 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: https://doi.org/10.1021/jo301309v. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://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: https://doi.org/10.1021/jo1025089. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://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: https://doi.org/10.1021/jo102413u. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://doi.org/10.1021/jo102413u
  • Source: Journal of Organic Chemistry. Unidades: IQ, FFCLRP

    Assunto: 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: https://doi.org/10.1021/jo201568n. Acesso em: 08 out. 2024.
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      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 out. 08 ] 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 out. 08 ] Available from: https://doi.org/10.1021/jo201568n
  • 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: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo100108b
  • 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: https://doi.org/10.1021/jo101227j. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://doi.org/10.1021/jo101227j
  • 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: https://doi.org/10.1021/jo1013405. Acesso em: 08 out. 2024.
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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 2024 out. 08 ] 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 out. 08 ] Available from: https://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: 08 out. 2024.
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      Bianco, G. G., Ferraz, H. M. C., Costa, A. M., Costa-Lotufo, L. V., 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, Costa-Lotufo LV, 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 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405
    • Vancouver

      Bianco GG, Ferraz HMC, Costa AM, Costa-Lotufo LV, 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 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: 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: mailto://wjbaader@iq.usp.br. Acesso em: 08 out. 2024.
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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 mailto://wjbaader@iq.usp.br
    • 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 2024 out. 08 ] Available from: mailto://wjbaader@iq.usp.br
    • 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 2024 out. 08 ] Available from: mailto://wjbaader@iq.usp.br
  • Source: Journal of Organic Chemistry. Unidades: FFCLRP, IQ, FCFRP

    Assunto: FOTOQUÍMICA

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      OLIVEIRA, Kleber Thiago de et al. Synthesis of phthalocyanines-ALA conjugates: water-soluble compounds with low aggregation. Journal of Organic Chemistry, v. 74, n. 20, p. 7962-7965, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/jo901633a. Acesso em: 08 out. 2024.
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      Oliveira, K. T. de, Assis, F. F. de A., Ribeiro, A. O., Neri, C. R., Fernandes, A. U., Baptista, M. da S., et al. (2009). Synthesis of phthalocyanines-ALA conjugates: water-soluble compounds with low aggregation. Journal of Organic Chemistry, 74( 20), 7962-7965. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/jo901633a
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      Oliveira KT de, Assis FF de A, Ribeiro AO, Neri CR, Fernandes AU, Baptista M da S, Lopes NP, Serra OA, Iamamoto Y. Synthesis of phthalocyanines-ALA conjugates: water-soluble compounds with low aggregation [Internet]. Journal of Organic Chemistry. 2009 ; 74( 20): 7962-7965.[citado 2024 out. 08 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo901633a
    • Vancouver

      Oliveira KT de, Assis FF de A, Ribeiro AO, Neri CR, Fernandes AU, Baptista M da S, Lopes NP, Serra OA, Iamamoto Y. Synthesis of phthalocyanines-ALA conjugates: water-soluble compounds with low aggregation [Internet]. Journal of Organic Chemistry. 2009 ; 74( 20): 7962-7965.[citado 2024 out. 08 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo901633a
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: METABÓLITOS SECUNDÁRIOS, HIDROCARBONOS, PENICILLIUM

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      FERRAZ, Helena Maria Carvalho e LONGO JR., Luiz Sidney. Bicyclic 'beta'-hydroxytetrahydrofurans as precursors of medium ring keto-lactones. Journal of Organic Chemistry, v. 72, n. 8, p. 2945-2950, 2007Tradução . . Acesso em: 08 out. 2024.
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      Ferraz, H. M. C., & Longo Jr., L. S. (2007). Bicyclic 'beta'-hydroxytetrahydrofurans as precursors of medium ring keto-lactones. Journal of Organic Chemistry, 72( 8), 2945-2950.
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      Ferraz HMC, Longo Jr. LS. Bicyclic 'beta'-hydroxytetrahydrofurans as precursors of medium ring keto-lactones. Journal of Organic Chemistry. 2007 ; 72( 8): 2945-2950.[citado 2024 out. 08 ]
    • Vancouver

      Ferraz HMC, Longo Jr. LS. Bicyclic 'beta'-hydroxytetrahydrofurans as precursors of medium ring keto-lactones. Journal of Organic Chemistry. 2007 ; 72( 8): 2945-2950.[citado 2024 out. 08 ]
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SOLVENTE

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      MARTINS, Clarissa Tavares e LIMA, Michelle de Souza e EL SEOUD, Omar A. Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry, v. 71, n. 24, p. 9068-9079, 2006Tradução . . Acesso em: 08 out. 2024.
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      Martins, C. T., Lima, M. de S., & El Seoud, O. A. (2006). Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry, 71( 24), 9068-9079.
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      Martins CT, Lima M de S, El Seoud OA. Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry. 2006 ; 71( 24): 9068-9079.[citado 2024 out. 08 ]
    • Vancouver

      Martins CT, Lima M de S, El Seoud OA. Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry. 2006 ; 71( 24): 9068-9079.[citado 2024 out. 08 ]
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: BIOQUÍMICA

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      MARCHETTO, Reinaldo et al. Determination of site-site distance and site concentration within polymer beads: a combined swelling-electron paramagnetic resonance study. Journal of Organic Chemistry, v. 70, n. 1, p. 110-114, 2005Tradução . . Acesso em: 08 out. 2024.
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      Marchetto, R., Cilli, E. M., Jubilut, G. N., Schreier, S., & Nakaie, C. R. (2005). Determination of site-site distance and site concentration within polymer beads: a combined swelling-electron paramagnetic resonance study. Journal of Organic Chemistry, 70( 1), 110-114.
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      Marchetto R, Cilli EM, Jubilut GN, Schreier S, Nakaie CR. Determination of site-site distance and site concentration within polymer beads: a combined swelling-electron paramagnetic resonance study. Journal of Organic Chemistry. 2005 ; 70( 1): 110-114.[citado 2024 out. 08 ]
    • Vancouver

      Marchetto R, Cilli EM, Jubilut GN, Schreier S, Nakaie CR. Determination of site-site distance and site concentration within polymer beads: a combined swelling-electron paramagnetic resonance study. Journal of Organic Chemistry. 2005 ; 70( 1): 110-114.[citado 2024 out. 08 ]

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