Filtros : "Chemical Science" Removido: "Kehr, Gerald" Limpar

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  • Source: Chemical Science. Unidade: IF

    Subjects: SIMETRIA, ELÉTRONS, SPIN

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      CHARRY, Jorge et al. The three-center two-positron bond. Chemical Science, n. 13, 2022Tradução . . Disponível em: https://doi.org/10.1039/D2SC04630J. Acesso em: 13 nov. 2024.
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      Charry, J., Moncada, F., Barborini, M., Pedraza-González, L. M., Varella, M. T. do N., Tkatchenko, A., & Reyes, A. (2022). The three-center two-positron bond. Chemical Science, ( 13). doi:10.1039/D2SC04630J
    • NLM

      Charry J, Moncada F, Barborini M, Pedraza-González LM, Varella MT do N, Tkatchenko A, Reyes A. The three-center two-positron bond [Internet]. Chemical Science. 2022 ;( 13):[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/D2SC04630J
    • Vancouver

      Charry J, Moncada F, Barborini M, Pedraza-González LM, Varella MT do N, Tkatchenko A, Reyes A. The three-center two-positron bond [Internet]. Chemical Science. 2022 ;( 13):[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/D2SC04630J
  • Source: Chemical Science. Unidade: IQSC

    Assunto: CATÁLISE

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      CAIUBY, Clarice Alves Dale e FURNIEL, Lucas Giani e BURTOLOSO, Antonio Carlos Bender. Asymmetric transformations from sulfoxonium ylides. Chemical Science, v. 13, p. 1192–1209, 2022Tradução . . Disponível em: https://doi.org/10.1039/D1SC05708A. Acesso em: 13 nov. 2024.
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      Caiuby, C. A. D., Furniel, L. G., & Burtoloso, A. C. B. (2022). Asymmetric transformations from sulfoxonium ylides. Chemical Science, 13, 1192–1209. doi:10.1039/D1SC05708A
    • NLM

      Caiuby CAD, Furniel LG, Burtoloso ACB. Asymmetric transformations from sulfoxonium ylides [Internet]. Chemical Science. 2022 ; 13 1192–1209.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/D1SC05708A
    • Vancouver

      Caiuby CAD, Furniel LG, Burtoloso ACB. Asymmetric transformations from sulfoxonium ylides [Internet]. Chemical Science. 2022 ; 13 1192–1209.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/D1SC05708A
  • Source: Chemical Science. Unidade: IQSC

    Subjects: COBRE, CATÁLISE

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      FURNIEL, Lucas G. e PEREZ, Radell Echemendía e BURTOLOSO, Antonio Carlos Bender. Cooperative copper-squaramide catalysis for the enantioselective N–H insertion reaction with sulfoxonium ylides. Chemical Science, v. 12, p. 7453-7459, 2021Tradução . . Disponível em: https://doi.org/10.1039/D1SC00979F. Acesso em: 13 nov. 2024.
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      Furniel, L. G., Perez, R. E., & Burtoloso, A. C. B. (2021). Cooperative copper-squaramide catalysis for the enantioselective N–H insertion reaction with sulfoxonium ylides. Chemical Science, 12, 7453-7459. doi:10.1039/D1SC00979F
    • NLM

      Furniel LG, Perez RE, Burtoloso ACB. Cooperative copper-squaramide catalysis for the enantioselective N–H insertion reaction with sulfoxonium ylides [Internet]. Chemical Science. 2021 ; 12 7453-7459.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/D1SC00979F
    • Vancouver

      Furniel LG, Perez RE, Burtoloso ACB. Cooperative copper-squaramide catalysis for the enantioselective N–H insertion reaction with sulfoxonium ylides [Internet]. Chemical Science. 2021 ; 12 7453-7459.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/D1SC00979F
  • Source: Chemical Science. Unidade: IF

    Assunto: POLARIZAÇÃO

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      MONCADA, Félix et al. Covalent bonds in positron dihalides. Chemical Science, v. 11, n. 1, p. 44–52, 2020Tradução . . Disponível em: https://doi.org/10.1039/c9sc04433g. Acesso em: 13 nov. 2024.
    • APA

      Moncada, F., Pedraza-González, L., Charry, J., Varella, M. T. do N., & Reyes, A. (2020). Covalent bonds in positron dihalides. Chemical Science, 11( 1), 44–52. doi:10.1039/c9sc04433g
    • NLM

      Moncada F, Pedraza-González L, Charry J, Varella MT do N, Reyes A. Covalent bonds in positron dihalides [Internet]. Chemical Science. 2020 ;11( 1): 44–52.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c9sc04433g
    • Vancouver

      Moncada F, Pedraza-González L, Charry J, Varella MT do N, Reyes A. Covalent bonds in positron dihalides [Internet]. Chemical Science. 2020 ;11( 1): 44–52.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c9sc04433g
  • Source: Chemical Science. Unidade: IFSC

    Subjects: ENZIMAS, ESCHERICHIA COLI, BACTÉRIAS GRAM-NEGATIVAS

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      MURILLO-LÓPEZ, Juliana et al. Studying the phosphoryl transfer mechanism of the E. coli phosphofructokinase-2: from X-ray structure to quantum mechanics/molecular mechanics simulations. Chemical Science, v. 10, n. 10, p. 2882-2892, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9sc00094a. Acesso em: 13 nov. 2024.
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      Murillo-López, J., Zinovjev, K., Pereira, H. d'M., Caniuguir, A., Garratt, R. C., Babul, J., et al. (2019). Studying the phosphoryl transfer mechanism of the E. coli phosphofructokinase-2: from X-ray structure to quantum mechanics/molecular mechanics simulations. Chemical Science, 10( 10), 2882-2892. doi:10.1039/c9sc00094a
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      Murillo-López J, Zinovjev K, Pereira H d'M, Caniuguir A, Garratt RC, Babul J, Recabarren R, Alzate-Morales J, Caballero J, Tuñón I, Cabrera R. Studying the phosphoryl transfer mechanism of the E. coli phosphofructokinase-2: from X-ray structure to quantum mechanics/molecular mechanics simulations [Internet]. Chemical Science. 2019 ; 10( 10): 2882-2892.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c9sc00094a
    • Vancouver

      Murillo-López J, Zinovjev K, Pereira H d'M, Caniuguir A, Garratt RC, Babul J, Recabarren R, Alzate-Morales J, Caballero J, Tuñón I, Cabrera R. Studying the phosphoryl transfer mechanism of the E. coli phosphofructokinase-2: from X-ray structure to quantum mechanics/molecular mechanics simulations [Internet]. Chemical Science. 2019 ; 10( 10): 2882-2892.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c9sc00094a
  • Source: Chemical Science. Unidade: IQ

    Subjects: POLIMERIZAÇÃO, MOLÉCULA

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      NOBREGA, Marcelo Medre et al. One-dimensional diamondoid polyaniline-like nanothreads from compressed crystal aniline. Chemical Science, v. 9, n. 1, p. 254-260, 2018Tradução . . Disponível em: https://doi.org/10.1039/c7sc03445h. Acesso em: 13 nov. 2024.
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      Nobrega, M. M., Teixeira Neto, É., Cairns, A. B., Temperini, M. L. A., & Bini, R. (2018). One-dimensional diamondoid polyaniline-like nanothreads from compressed crystal aniline. Chemical Science, 9( 1), 254-260. doi:10.1039/c7sc03445h
    • NLM

      Nobrega MM, Teixeira Neto É, Cairns AB, Temperini MLA, Bini R. One-dimensional diamondoid polyaniline-like nanothreads from compressed crystal aniline [Internet]. Chemical Science. 2018 ; 9( 1): 254-260.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c7sc03445h
    • Vancouver

      Nobrega MM, Teixeira Neto É, Cairns AB, Temperini MLA, Bini R. One-dimensional diamondoid polyaniline-like nanothreads from compressed crystal aniline [Internet]. Chemical Science. 2018 ; 9( 1): 254-260.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c7sc03445h
  • Source: Chemical Science. Unidade: IQ

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, ORBITAL MOLECULAR

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      VIESSER, Renan V et al. The unexpected roles of sigma and pi orbitals in electron donor and acceptor group effects on the C-13 NMR chemical shifts in substituted benzenest. Chemical Science, v. 8, n. 9, p. 6570-6576, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7sc02163a. Acesso em: 13 nov. 2024.
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      Viesser, R. V., Ducati, L. C., Tormena, C. F., & Autschbach, J. (2017). The unexpected roles of sigma and pi orbitals in electron donor and acceptor group effects on the C-13 NMR chemical shifts in substituted benzenest. Chemical Science, 8( 9), 6570-6576. doi:10.1039/c7sc02163a
    • NLM

      Viesser RV, Ducati LC, Tormena CF, Autschbach J. The unexpected roles of sigma and pi orbitals in electron donor and acceptor group effects on the C-13 NMR chemical shifts in substituted benzenest [Internet]. Chemical Science. 2017 ; 8( 9): 6570-6576.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c7sc02163a
    • Vancouver

      Viesser RV, Ducati LC, Tormena CF, Autschbach J. The unexpected roles of sigma and pi orbitals in electron donor and acceptor group effects on the C-13 NMR chemical shifts in substituted benzenest [Internet]. Chemical Science. 2017 ; 8( 9): 6570-6576.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c7sc02163a
  • Source: Chemical Science. Unidade: IQSC

    Assunto: DNA

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      LAUER, Milena Helmer et al. Methyltransferase-directed covalent coupling of fluorophores to DNA. Chemical Science, v. 8, n. 5, p. 3804-3811, 2017Tradução . . Disponível em: https://doi.org/10.1039/c6sc04229e. Acesso em: 13 nov. 2024.
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      Lauer, M. H., Vranken, C., Deen, J., Frederickx, W., Vanderline, F. A., Wand, N., et al. (2017). Methyltransferase-directed covalent coupling of fluorophores to DNA. Chemical Science, 8( 5), 3804-3811. doi:10.1039/c6sc04229e
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      Lauer MH, Vranken C, Deen J, Frederickx W, Vanderline FA, Wand N, Leen V, Gehlen MH, Hofkens J, Neely RK. Methyltransferase-directed covalent coupling of fluorophores to DNA [Internet]. Chemical Science. 2017 ; 8( 5): 3804-3811.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c6sc04229e
    • Vancouver

      Lauer MH, Vranken C, Deen J, Frederickx W, Vanderline FA, Wand N, Leen V, Gehlen MH, Hofkens J, Neely RK. Methyltransferase-directed covalent coupling of fluorophores to DNA [Internet]. Chemical Science. 2017 ; 8( 5): 3804-3811.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c6sc04229e
  • Source: Chemical Science. Unidade: IFSC

    Subjects: FLUORESCÊNCIA, ESPECTROSCOPIA

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      MATUSCHEK, David et al. Profluorescent verdazyl radicals: synthesis and characterization. Chemical Science, v. 6, n. 8, p. 4712-4716, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5sc00724k. Acesso em: 13 nov. 2024.
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      Matuschek, D., Eusterwiemann, S., Stegemann, L., Doerenkamp, C., Wibbeling, B., Daniliuc, C. G., et al. (2015). Profluorescent verdazyl radicals: synthesis and characterization. Chemical Science, 6( 8), 4712-4716. doi:10.1039/c5sc00724k
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      Matuschek D, Eusterwiemann S, Stegemann L, Doerenkamp C, Wibbeling B, Daniliuc CG, Doltsinis NL, Strassert CA, Eckert H, Studer A. Profluorescent verdazyl radicals: synthesis and characterization [Internet]. Chemical Science. 2015 ; 6( 8): 4712-4716.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c5sc00724k
    • Vancouver

      Matuschek D, Eusterwiemann S, Stegemann L, Doerenkamp C, Wibbeling B, Daniliuc CG, Doltsinis NL, Strassert CA, Eckert H, Studer A. Profluorescent verdazyl radicals: synthesis and characterization [Internet]. Chemical Science. 2015 ; 6( 8): 4712-4716.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c5sc00724k
  • Source: Chemical Science. Unidade: IQSC

    Assunto: ELETROQUÍMICA

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      SOUZA-GARCIA, Janaina et al. Mechanistic changes observed in heavy water for nitrate reduction reaction on palladium-modified Pt(hkl) electrodes. Chemical Science, v. 3, p. 3063-3070, 2012Tradução . . Disponível em: https://doi.org/10.1039/c2sc20490h. Acesso em: 13 nov. 2024.
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      Souza-Garcia, J., Ticianelli, E. A., Climent, V., & Feliu, J. M. (2012). Mechanistic changes observed in heavy water for nitrate reduction reaction on palladium-modified Pt(hkl) electrodes. Chemical Science, 3, 3063-3070. doi:10.1039/c2sc20490h
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      Souza-Garcia J, Ticianelli EA, Climent V, Feliu JM. Mechanistic changes observed in heavy water for nitrate reduction reaction on palladium-modified Pt(hkl) electrodes [Internet]. Chemical Science. 2012 ; 3 3063-3070.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c2sc20490h
    • Vancouver

      Souza-Garcia J, Ticianelli EA, Climent V, Feliu JM. Mechanistic changes observed in heavy water for nitrate reduction reaction on palladium-modified Pt(hkl) electrodes [Internet]. Chemical Science. 2012 ; 3 3063-3070.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c2sc20490h
  • Source: Chemical Science. Unidade: FCFRP

    Subjects: TRYPANOSOMA CRUZI, QUÍMICA FARMACÊUTICA

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      CAMPO, Vanessa L. et al. Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase. Chemical Science, n. 4, p. 507-514, 2010Tradução . . Disponível em: https://doi.org/10.1039/c0sc00301h. Acesso em: 13 nov. 2024.
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      Campo, V. L., Carvalho, I., Silva, C. H. T. de P. da, Schenkman, S., Hill, L., Nepogodiev, S. A., & Field, R. A. (2010). Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase. Chemical Science, ( 4), 507-514. doi:10.1039/c0sc00301h
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      Campo VL, Carvalho I, Silva CHT de P da, Schenkman S, Hill L, Nepogodiev SA, Field RA. Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase [Internet]. Chemical Science. 2010 ;( 4): 507-514.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c0sc00301h
    • Vancouver

      Campo VL, Carvalho I, Silva CHT de P da, Schenkman S, Hill L, Nepogodiev SA, Field RA. Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase [Internet]. Chemical Science. 2010 ;( 4): 507-514.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1039/c0sc00301h

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