Filtros : "Zukerman-Schpector, Júlio" Removidos: "GRU999" "IQ-USP" Limpar

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  • Source: Physical Chemistry Chemical Physics. Unidade: IF

    Assunto: TERMODINÂMICA (FÍSICO-QUÍMICA)

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      FREIRE, Thales Souza et al. Structural and thermodynamic characterization of allosteric transitions in human serum albumin with metadynamics simulations. Physical Chemistry Chemical Physics, n. 7, p. 6436-6447, 2024Tradução . . Disponível em: https://doi.org/10.1039/D3CP04169G. Acesso em: 06 nov. 2024.
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      Freire, T. S., Zukerman-Schpector, J., Friedman, R., & Caracelli, I. (2024). Structural and thermodynamic characterization of allosteric transitions in human serum albumin with metadynamics simulations. Physical Chemistry Chemical Physics, ( 7), 6436-6447. doi:10.1039/D3CP04169G
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      Freire TS, Zukerman-Schpector J, Friedman R, Caracelli I. Structural and thermodynamic characterization of allosteric transitions in human serum albumin with metadynamics simulations [Internet]. Physical Chemistry Chemical Physics. 2024 ;( 7): 6436-6447.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/D3CP04169G
    • Vancouver

      Freire TS, Zukerman-Schpector J, Friedman R, Caracelli I. Structural and thermodynamic characterization of allosteric transitions in human serum albumin with metadynamics simulations [Internet]. Physical Chemistry Chemical Physics. 2024 ;( 7): 6436-6447.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/D3CP04169G
  • Source: Acta Crystallographica Section E Crystallographic Communications. Unidade: IQSC

    Assunto: CRISTALOGRAFIA

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      PEDROSO, Sofia Dallasta et al. 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2- dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry. Acta Crystallographica Section E Crystallographic Communications, v. E76, p. 967-972, 2020Tradução . . Disponível em: https://doi.org/10.1107/S205698902000701X. Acesso em: 06 nov. 2024.
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      Pedroso, S. D., Caracelli, I., Zukerman-Schpector, J., Soto-Monsalve, M., Santos, R. H. de A., Correia, C. R. D., et al. (2020). 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2- dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry. Acta Crystallographica Section E Crystallographic Communications, E76, 967-972. doi:10.1107/S205698902000701X
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      Pedroso SD, Caracelli I, Zukerman-Schpector J, Soto-Monsalve M, Santos RH de A, Correia CRD, Garcia ALL, Kwong HC, Tiekink ERT. 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2- dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry [Internet]. Acta Crystallographica Section E Crystallographic Communications. 2020 ; E76 967-972.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/S205698902000701X
    • Vancouver

      Pedroso SD, Caracelli I, Zukerman-Schpector J, Soto-Monsalve M, Santos RH de A, Correia CRD, Garcia ALL, Kwong HC, Tiekink ERT. 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2- dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry [Internet]. Acta Crystallographica Section E Crystallographic Communications. 2020 ; E76 967-972.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/S205698902000701X
  • Source: ChemCatChem. Unidades: FCF, IQ

    Subjects: LIGANTES, CATALISADORES

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      OLIVEIRA, Isadora Maria de et al. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, v. 12, p. 3545–3552, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.202000395. Acesso em: 06 nov. 2024.
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      Oliveira, I. M. de, Esteves, H. A., Darbem, M. P., Sartorelli, A., Correra, T. C., Oliveira, A. F. R., et al. (2020). Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, 12, 3545–3552. doi:10.1002/cctc.202000395
    • NLM

      Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/cctc.202000395
    • Vancouver

      Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/cctc.202000395
  • Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC

    Subjects: ALDEÍDOS, ESTEREOQUÍMICA

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      VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 06 nov. 2024.
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      Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Pimenta, D. C., & Stefani, H. A. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564
    • NLM

      Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/adsc.201900564
    • Vancouver

      Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/adsc.201900564
  • Source: New Journal of Chemistry. Unidade: FCF

    Subjects: SELÊNIO, ESTEREOQUÍMICA

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      OLIVEIRA, Isadora Maria de et al. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, v. 42, n. 12, p. 10118-10123, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8nj01543k. Acesso em: 06 nov. 2024.
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      Oliveira, I. M. de, Pimenta, D. C., Zukerman-Schpector, J., Stefani, H. A., & Manarin, F. (2018). Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, 42( 12), 10118-10123. doi:10.1039/c8nj01543k
    • NLM

      Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/c8nj01543k
    • Vancouver

      Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/c8nj01543k
  • Source: Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. Unidade: IQSC

    Assunto: CRISTALOGRAFIA

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      ZUKERMAN-SCHPECTOR, Júlio et al. (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, v. E74, p. 414-418, 2018Tradução . . Disponível em: https://doi.org/10.1107/S2056989018003092. Acesso em: 06 nov. 2024.
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      Zukerman-Schpector, J., Monsalve, M. S., Santos, R. H. de A., Machado, A. H. L., Correia, C. R. D., Jotani , M. M., & Tiekink, E. R. T. (2018). (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, E74, 414-418. doi:10.1107/S2056989018003092
    • NLM

      Zukerman-Schpector J, Monsalve MS, Santos RH de A, Machado AHL, Correia CRD, Jotani MM, Tiekink ERT. (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; E74 414-418.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/S2056989018003092
    • Vancouver

      Zukerman-Schpector J, Monsalve MS, Santos RH de A, Machado AHL, Correia CRD, Jotani MM, Tiekink ERT. (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; E74 414-418.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/S2056989018003092
  • Source: Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. Unidade: IQSC

    Assunto: CRISTALOGRAFIA

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      ZUKERMAN-SCHPECTOR, Júlio et al. (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, p. 371-375, 2018Tradução . . Disponível em: https://doi.org/10.1107/S2056989018002451. Acesso em: 06 nov. 2024.
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      Zukerman-Schpector, J., Monsalve, M. S., Santos, R. H. de A., Garcia, A. L. L., Correia, C. R. D., Jotani , M. M., & Tiekink, E. R. T. (2018). (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, 371-375. doi:10.1107/S2056989018002451
    • NLM

      Zukerman-Schpector J, Monsalve MS, Santos RH de A, Garcia ALL, Correia CRD, Jotani MM, Tiekink ERT. (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; 371-375.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/S2056989018002451
    • Vancouver

      Zukerman-Schpector J, Monsalve MS, Santos RH de A, Garcia ALL, Correia CRD, Jotani MM, Tiekink ERT. (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; 371-375.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/S2056989018002451
  • Source: Synthesis. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 06 nov. 2024.
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      Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
    • NLM

      Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1055/s-0036-1589090
    • Vancouver

      Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1055/s-0036-1589090
  • Source: ChemistrySelect. Unidade: FCF

    Subjects: PALÁDIO, QUÍMICA FARMACÊUTICA

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      BARBEIRO, Cristiane de Souza et al. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, v. 2, n. 26, p. 8173-8177, 2017Tradução . . Disponível em: https://doi.org/10.1002/slct.201701197. Acesso em: 06 nov. 2024.
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      Barbeiro, C. de S., Vasconcelos, S. N. S., Oliveira, I. M. de, Zukerman-Schpector, J., Caracelli, I., Maganhi, S. H., & Stefani, H. A. (2017). Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, 2( 26), 8173-8177. doi:10.1002/slct.201701197
    • NLM

      Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/slct.201701197
    • Vancouver

      Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/slct.201701197
  • Source: Zeitschrift fur Kristallographie - Crystalline Materials. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, COMPOSTOS ORGÂNICOS

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      CARACELLI, Ignez et al. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound. Zeitschrift fur Kristallographie - Crystalline Materials, v. 231, n. 6, p. 321–328, 2016Tradução . . Disponível em: https://doi.org/10.1515/zkri-2016-1931. Acesso em: 06 nov. 2024.
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      Caracelli, I., Zukerman-Schpector, J., Madureira, L. S., Maganhi, S. H., Stefani, H. A., Guadagnin, R. C., & Tiekink, E. R. T. (2016). Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound. Zeitschrift fur Kristallographie - Crystalline Materials, 231( 6), 321–328. doi:10.1515/zkri-2016-1931
    • NLM

      Caracelli I, Zukerman-Schpector J, Madureira LS, Maganhi SH, Stefani HA, Guadagnin RC, Tiekink ERT. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound [Internet]. Zeitschrift fur Kristallographie - Crystalline Materials. 2016 ; 231( 6): 321–328.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1515/zkri-2016-1931
    • Vancouver

      Caracelli I, Zukerman-Schpector J, Madureira LS, Maganhi SH, Stefani HA, Guadagnin RC, Tiekink ERT. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound [Internet]. Zeitschrift fur Kristallographie - Crystalline Materials. 2016 ; 231( 6): 321–328.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1515/zkri-2016-1931
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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      SHAMIM, Anwar et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 06 nov. 2024.
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      Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052
    • NLM

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
    • Vancouver

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
  • Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química (SBQ). Unidade: IQ

    Subjects: INFRAVERMELHO, ESPECTROSCOPIA

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      TRAESEL, Henrique Joel et al. Síntese e estudo conformacional da α-metoxi-α-fenilseleno-acetofenona. 2014, Anais.. São Paulo: Sociedade Brasileira de Química (SBQ), 2014. . Acesso em: 06 nov. 2024.
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      Traesel, H. J., Olivato, P. R., Rodrigues, D. N. S., Valença, J., & Zukerman-Schpector, J. (2014). Síntese e estudo conformacional da α-metoxi-α-fenilseleno-acetofenona. In Resumos. São Paulo: Sociedade Brasileira de Química (SBQ).
    • NLM

      Traesel HJ, Olivato PR, Rodrigues DNS, Valença J, Zukerman-Schpector J. Síntese e estudo conformacional da α-metoxi-α-fenilseleno-acetofenona. Resumos. 2014 ;[citado 2024 nov. 06 ]
    • Vancouver

      Traesel HJ, Olivato PR, Rodrigues DNS, Valença J, Zukerman-Schpector J. Síntese e estudo conformacional da α-metoxi-α-fenilseleno-acetofenona. Resumos. 2014 ;[citado 2024 nov. 06 ]
  • Source: Acta Crystallographica Section E. Unidade: IQ

    Assunto: COMPOSTOS ORGÂNICOS

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      ZUKERMAN-SCHPECTOR, Júlio et al. 3,3-Bis(4-bromophenylsulfanyl)-1-methylpiperidin-2-one. Acta Crystallographica Section E, v. E69, p. 0556 : + Supplementary materials ( S1-S7), 2013Tradução . . Disponível em: https://doi.org/10.1107/s1600536813006995. Acesso em: 06 nov. 2024.
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      Zukerman-Schpector, J., Olivato, P. R., Cerqueira Júnior, C. R., Contieri, B., Ng, S. W., & Tiekink, E. R. T. (2013). 3,3-Bis(4-bromophenylsulfanyl)-1-methylpiperidin-2-one. Acta Crystallographica Section E, E69, 0556 : + Supplementary materials ( S1-S7). doi:10.1107/s1600536813006995
    • NLM

      Zukerman-Schpector J, Olivato PR, Cerqueira Júnior CR, Contieri B, Ng SW, Tiekink ERT. 3,3-Bis(4-bromophenylsulfanyl)-1-methylpiperidin-2-one [Internet]. Acta Crystallographica Section E. 2013 ; E69 0556 : + Supplementary materials ( S1-S7).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/s1600536813006995
    • Vancouver

      Zukerman-Schpector J, Olivato PR, Cerqueira Júnior CR, Contieri B, Ng SW, Tiekink ERT. 3,3-Bis(4-bromophenylsulfanyl)-1-methylpiperidin-2-one [Internet]. Acta Crystallographica Section E. 2013 ; E69 0556 : + Supplementary materials ( S1-S7).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1107/s1600536813006995
  • Source: European Journal of Organic Chemistry. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, TELÚRIO

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      STEFANI, Hélio Alexandre et al. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction. European Journal of Organic Chemistry, n. 18, p. 3780-3783, 2013Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201300009. Acesso em: 06 nov. 2024.
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      Stefani, H. A., Vasconcelos, S. N. S., Manarin, F., Leal, D. M., Souza, F. B., Madureira, L. S., et al. (2013). Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction. European Journal of Organic Chemistry, ( 18), 3780-3783. doi:10.1002/ejoc.201300009
    • NLM

      Stefani HA, Vasconcelos SNS, Manarin F, Leal DM, Souza FB, Madureira LS, Zukerman-Schpector J, Eberlin MN, Godoi MN, Galaverna R de S. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction [Internet]. European Journal of Organic Chemistry. 2013 ;( 18): 3780-3783.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/ejoc.201300009
    • Vancouver

      Stefani HA, Vasconcelos SNS, Manarin F, Leal DM, Souza FB, Madureira LS, Zukerman-Schpector J, Eberlin MN, Godoi MN, Galaverna R de S. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction [Internet]. European Journal of Organic Chemistry. 2013 ;( 18): 3780-3783.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/ejoc.201300009
  • Source: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. Unidade: IQ

    Subjects: ESPECTROSCOPIA INFRAVERMELHA, DIFRAÇÃO POR RAIOS X

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      VINHATO, Elisângela et al. Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, v. 115, p. 738-746, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2013.06.118. Acesso em: 06 nov. 2024.
    • APA

      Vinhato, E., Olivato, P. R., Zukerman-Schpector, J., & Dal Colle, M. (2013). Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 115, 738-746. doi:10.1016/j.saa.2013.06.118
    • NLM

      Vinhato E, Olivato PR, Zukerman-Schpector J, Dal Colle M. Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides [Internet]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2013 ; 115 738-746.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.saa.2013.06.118
    • Vancouver

      Vinhato E, Olivato PR, Zukerman-Schpector J, Dal Colle M. Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides [Internet]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2013 ; 115 738-746.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.saa.2013.06.118
  • Source: Molecules. Unidade: IQ

    Subjects: ESPECTROSCOPIA INFRAVERMELHA, DIFRAÇÃO POR RAIOS X

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      OLIVATO, Paulo Roberto et al. Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones. Molecules, v. 18, n. 7, p. 7492-7509, 2013Tradução . . Disponível em: https://doi.org/10.3390/molecules18077492. Acesso em: 06 nov. 2024.
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      Olivato, P. R., Santos, J. M. M., Contieri, B., Cerqueira Júnior, C. R., Rodrigues, D. N. S., Vinhato, E., et al. (2013). Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones. Molecules, 18( 7), 7492-7509. doi:10.3390/molecules18077492
    • NLM

      Olivato PR, Santos JMM, Contieri B, Cerqueira Júnior CR, Rodrigues DNS, Vinhato E, Zukerman-Schpector J, Dal Colle M. Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones [Internet]. Molecules. 2013 ; 18( 7): 7492-7509.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/molecules18077492
    • Vancouver

      Olivato PR, Santos JMM, Contieri B, Cerqueira Júnior CR, Rodrigues DNS, Vinhato E, Zukerman-Schpector J, Dal Colle M. Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones [Internet]. Molecules. 2013 ; 18( 7): 7492-7509.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/molecules18077492
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      STEFANI, Hélio Alexandre et al. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, v. 54, n. 43, p. 5821-5825, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.064. Acesso em: 06 nov. 2024.
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      Stefani, H. A., Vasconcelos, S. N. S., Souza, F. B., Manarin, F., & Zukerman-Schpector, J. (2013). One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, 54( 43), 5821-5825. doi:10.1016/j.tetlet.2013.08.064
    • NLM

      Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
    • Vancouver

      Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
  • Source: Symposium Materials. Conference titles: International Symposium on the Organic Chemistry of Sulfur. Unidade: IQ

    Subjects: ESPECTROSCOPIA INFRAVERMELHA, QUÍMICA ORGÂNICA

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    • ABNT

      OLIVATO, Paulo Roberto et al. Conformational preferences for some 3-(4'-substituted phenylsulfonyl)-1-methyl-2-piperidones through spectroscopic and theoretical studies. 2012, Anais.. Czestochowa: Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, 2012. . Acesso em: 06 nov. 2024.
    • APA

      Olivato, P. R., Santos, J. M. M., Cerqueira Júnior, C. R., Vinhato, E., Zukerman-Schpector, J., & Dal Colle, M. (2012). Conformational preferences for some 3-(4'-substituted phenylsulfonyl)-1-methyl-2-piperidones through spectroscopic and theoretical studies. In Symposium Materials. Czestochowa: Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences.
    • NLM

      Olivato PR, Santos JMM, Cerqueira Júnior CR, Vinhato E, Zukerman-Schpector J, Dal Colle M. Conformational preferences for some 3-(4'-substituted phenylsulfonyl)-1-methyl-2-piperidones through spectroscopic and theoretical studies. Symposium Materials. 2012 ;[citado 2024 nov. 06 ]
    • Vancouver

      Olivato PR, Santos JMM, Cerqueira Júnior CR, Vinhato E, Zukerman-Schpector J, Dal Colle M. Conformational preferences for some 3-(4'-substituted phenylsulfonyl)-1-methyl-2-piperidones through spectroscopic and theoretical studies. Symposium Materials. 2012 ;[citado 2024 nov. 06 ]
  • Source: Anais. Conference titles: Congresso Brasileiro de Química. Unidade: IQ

    Subjects: ANTI-INFLAMATÓRIOS, INIBIDORES DE ENZIMAS

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      BAPTISITNI, N et al. Docking molecular de compostos organocalcogênios anti-inflamatórios na enzima COX-2. 2012, Anais.. Rio de Janeiro: Associação Brasileira de Química (ABQ), 2012. . Acesso em: 06 nov. 2024.
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      Baptisitni, N., Caracelli, I., Zukerman-Schpector, J., Olivato, P. R., & Cerqueira Júnior, C. R. (2012). Docking molecular de compostos organocalcogênios anti-inflamatórios na enzima COX-2. In Anais. Rio de Janeiro: Associação Brasileira de Química (ABQ).
    • NLM

      Baptisitni N, Caracelli I, Zukerman-Schpector J, Olivato PR, Cerqueira Júnior CR. Docking molecular de compostos organocalcogênios anti-inflamatórios na enzima COX-2. Anais. 2012 ;[citado 2024 nov. 06 ]
    • Vancouver

      Baptisitni N, Caracelli I, Zukerman-Schpector J, Olivato PR, Cerqueira Júnior CR. Docking molecular de compostos organocalcogênios anti-inflamatórios na enzima COX-2. Anais. 2012 ;[citado 2024 nov. 06 ]
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      STEFANI, Hélio Alexandre et al. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, v. 53, n. 14, p. 1742-1747 : + Supplementary materials ( S1-S36), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.01.102. Acesso em: 06 nov. 2024.
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      Stefani, H. A., Silva, N. C. da S. e, Manarin, F., Lüdtke, D., Zukerman-Schpector, J., Madureira, L. S., & Tiekink, E. R. T. (2012). Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, 53( 14), 1742-1747 : + Supplementary materials ( S1-S36). doi:10.1016/j.tetlet.2012.01.102
    • NLM

      Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
    • Vancouver

      Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102

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