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  • Source: Journal of Organic Chemistry. Unidade: IQ

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

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    • ABNT

      SILVA, Sandra M. da; LANG, André Passaretti; SANTOS, Ana Paula Fileno dos; et al. Cyclic peroxidic carbon dioxide dimer fuels peroxyoxalate chemiluminescence. Journal of Organic Chemistry, Washington, v. 86, n. 17, p. 11434–11441, 2021. Disponível em: < https://dx.doi.org/10.1021/acs.joc.1c00929 > DOI: 10.1021/acs.joc.1c00929.
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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.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.Available from: https://dx.doi.org/10.1021/acs.joc.1c00929
  • Source: Journal of Organic Chemistry. Unidade: IQSC

    Assunto: QUÍMICA ORGÂNICA

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      NAGYMIHALY, Zoltan; CATURELLO, Naidel A. M. S.; TAKATSY, Aniko; et al. Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform. Journal of Organic Chemistry, Washington, v. 82, n. 1, 2017. Disponível em: < http://dx.doi.org/10.1021/acs.joc.6b02472 > DOI: 10.1021/acs.joc.6b02472.
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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):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):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; ANGNES, Ricardo A; SILVA, Vitor Hugo Menezes da; 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, Washington, v. 81, n. 5, p. 2010-2018, 2016. Disponível em: < http://dx.doi.org/10.1021/acs.joc.5b02846 > DOI: 10.1021/acs.joc.5b02846.
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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.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.Available from: http://dx.doi.org/10.1021/acs.joc.5b02846
  • Source: Journal of Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      KAWAMURA, Meire Yasuko; TALERO, Alexánder G; SANTIAGO, João V; et al. Six-step syntheses of (-)-1-deoxyaltronojirimycin and (+)-1-deoxymannonojirmycin from N-Z-O-TBDPS-L-serinal. Journal of Organic Chemistry, Washington, v. 81, n. 21, p. 10569-10575, 2016. Disponível em: < http://dx.doi.org/10.1021/acs.joc.6b01575 > DOI: 10.1021/acs.joc.6b01575.
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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.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.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.; RUIZ, Ana Lúcia T. G.; VENDRAMINI-COSTA, Débora B.; et al. Diastereoselective synthesis of biologically active cyclopenta[b]indoles. Journal of Organic Chemistry, Washington, DC, v. 81, n. 15, p. 6626-6639, 2016. Disponível em: < http://dx.doi.org/10.1021/acs.joc.6b01270 > DOI: 10.1021/acs.joc.6b01270.
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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.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.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; SILVA JUNIOR, Luiz Fernando da. Metal-Free asymmetric synthesis of indanes through chiral hypervalent iodine(III)-mediated ring contraction. Journal of Organic Chemistry, Washington, v. 81, p. 2174−2181, 2016. Disponível em: < http://dx.doi.org/10.1021/acs.joc.5b02803 > DOI: 10.1021/acs.joc.5b02803.
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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.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.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; OLIVEIRA, Marcelo Almeida de; CISCATO, Luiz Francisco Monteiro Leite; et al. Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects. Journal of Organic Chemistry, Washington, v. 80, n. 8, p. 3745-3751, 2015. Disponível em: < http://dx.doi.org/10.1021/acs.joc.5b00515 > DOI: 10.1021/acs.joc.5b00515.
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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.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.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; LIMA, Filipe da Silva; DIAS, Luís Gustavo; et al. Molecular dynamics simulations of the initial-state predict product distributions of dediazoniation of aryldiazonium in binary solvents. Journal of Organic Chemistry, Washington, v. 80, n. 17, p. 8637-8642, 2015. Disponível em: < http://dx.doi.org/10.1021/acs.joc.5b01289 > DOI: 10.1021/acs.joc.5b01289.
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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.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.Available from: http://dx.doi.org/10.1021/acs.joc.5b01289
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: FOTOQUÍMICA

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      OLIVEIRA, Marilene Silva; GHOGARE, Ashwini A; ABRAMOVA, Inna; et al. Mechanism of photochemical O-atom exchange in nitrosamines with molecular oxygen. Journal of Organic Chemistry, Washington, v. 80, n. 12, p. 6119-6127, 2015. Disponível em: < http://dx.doi.org/10.1021/acs.joc.5b00633 > DOI: 10.1021/acs.joc.5b00633.
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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.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.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; SILVA, Sandra Maria da; BAADER, Wilhelm Josef. Solvent cage effects: basis of a general mechanism for efficient chemiluminescence. Journal of Organic Chemistry, Washington, v. 78, n. 9, p. 4432-4439, 2013. Disponível em: < http://dx.doi.org/10.1021/jo400426y > DOI: 10.1021/jo400426y.
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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.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.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; HELENO, Vladimir Constantino Gomes; CAVALCANTE, Simone; et al. Solvent effect in reactions using Stryker's reagent. Journal of Organic Chemistry, Washington, v. 77, n. 20, p. 9374-9378, 2012. Disponível em: < http://dx.doi.org/10.1021/jo301595b >.
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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.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.Available from: http://dx.doi.org/10.1021/jo301595b
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: LUMINESCÊNCIA

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      OLIVEIRA, Marcelo Almeida de; BARTOLONI, Fernando Heering; AUGUSTO, Felipe Alberto; et al. Revision of singlet quantum yields in the catalyzed decomposition of cyclic peroxides. Journal of Organic Chemistry, Washington, v. 77, n. 23, p. 10537-10544, 2012. Disponível em: < http://dx.doi.org/10.1021/jo301309v > DOI: 10.1021/jo301309v.
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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.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.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; BATISTA, Andrea N. L; MOTA, Jonas da Silva; et al. Structure elucidation and absolute stereochemistry of isomeric monoterpene chromane esters. Journal of Organic Chemistry, Washington, v. 76, n. 8, p. 2603-2612, 2011. Disponível em: < http://dx.doi.org/10.1021/jo1025089 > DOI: 10.1021/jo1025089.
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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.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.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; SILVA JUNIOR, Luiz Fernando da; GIANNIS, Athanassios. Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III). Journal of Organic Chemistry, Washington, v. 76, n. 5, p. 1499-1502, 2011. Disponível em: < http://dx.doi.org/10.1021/jo102413u > DOI: 10.1021/jo102413u.
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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.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.Available from: http://dx.doi.org/10.1021/jo102413u
  • Source: Journal of Organic Chemistry. Unidades: IQ, FFCLRP

    Assunto: TERAPIA FOTODINÂMICA

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      UCHOA, Adjaci Fernandes; IAMAMOTO, Yassuko; SERRA, Osvaldo Antonio; et al. Chlorin photosensitizers sterically designed to prevent self-aggregation. Journal of Organic Chemistry, Washington, v. 76, n. 21, p. 8824-8832, 2011. Disponível em: < http://dx.doi.org/10.1021/jo201568n > DOI: 10.1021/jo201568n.
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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.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.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; CARNEIRO, Vânia Maria Teixeira; SILVA JR., Luiz Fernando da; OLOFSSON, Berit. Facile synthesis of koser’s reagent and derivatives from iodine or aryl iodides. Journal of Organic Chemistry, Washington, v. 75, n. 21, p. 7416-7419, 2010. Disponível em: < http://dx.doi.org/10.1021/jo101227j > DOI: 10.1021/jo101227j.
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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
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      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.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.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; FERRAZ, Helena Maria Carvalho; VIEIRA, Tiago de Oliveira; ISHIKAWA, Eloisa Erika; SILVA JUNIOR, Luiz Fernando da. A ring contraction strategy toward a diastereoselective total synthesis of (+)-bakkenolide A. Journal of Organic Chemistry, Washington, v. 75, n. 9, p. 2877-2882, 2010. Disponível em: < http://pubs.acs.org/doi/pdfplus/10.1021/jo100108b >.
    • 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.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.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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    • ABNT

      CISCATO, Luiz Francisco Monteiro Leite; BARTOLONI, Fernando Heering; WEISS, Dieter; BECKERT, Rainer; BAADER, Wilhelm Josef. Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition. Journal of Organic Chemistry, Washington, v. 75, n. 19, p. 6574-6580, 2010. Disponível em: < http://dx.doi.org/10.1021/jo1013405 > DOI: 10.1021/jo1013405.
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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.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.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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    • ABNT

      BIANCO, Graziela Gallego; FERRAZ, Helena Maria Carvalho; COSTA, Arinice M.; et al. (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity. Journal of Organic Chemistry, Washington, v. 74, n. 6, p. 2561-2566, 2009. Disponível em: < http://pubs.acs.org/doi/pdf/10.1021/jo9000405 >.
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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.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.Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: FOTOQUÍMICA

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    • ABNT

      CISCATO, Luiz Francisco Monteiro Leite; BARTOLONI, Fernando Heering; BASTOS, Erick Leite; BAADER, Wilhelm Josef. Direct kinetic observation of the chemiexcitation step in peroxyoxalate chemiluminescence. Journal of Organic Chemistry, Washington, v. 74, n. 23, p. 8974-8979, 2009. Disponível em: < http://pubs.acs.org/doi/pdfplus/10.1021/jo901402k >.
    • APA

      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.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.Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jo901402k

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