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  • Source: Chemical Science. Unidade: IQSC

    Subject: 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, 2022Tradução . . Disponível em: https://doi.org/10.1039/D1SC05708A. Acesso em: 04 out. 2022.
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      Caiuby, C. A. D., Furniel, L. G., & Burtoloso, A. C. B. (2022). Asymmetric transformations from sulfoxonium ylides. Chemical Science, 13. doi:10.1039/D1SC05708A
    • NLM

      Caiuby CAD, Furniel LG, Burtoloso ACB. Asymmetric transformations from sulfoxonium ylides [Internet]. Chemical Science. 2022 ; 13[citado 2022 out. 04 ] 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[citado 2022 out. 04 ] 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: 04 out. 2022.
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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 2022 out. 04 ] 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 2022 out. 04 ] Available from: https://doi.org/10.1039/D1SC00979F
  • Source: Chemical Science. Unidade: IF

    Subject: 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://repositorio.usp.br/directbitstream/43a6c004-e069-472a-bd13-b63bff22d837/c9sc04433g.pdf. Acesso em: 04 out. 2022.
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      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
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      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 2022 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/43a6c004-e069-472a-bd13-b63bff22d837/c9sc04433g.pdf
    • 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 2022 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/43a6c004-e069-472a-bd13-b63bff22d837/c9sc04433g.pdf
  • 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: http://dx.doi.org/10.1039/c9sc00094a. Acesso em: 04 out. 2022.
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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
    • NLM

      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 2022 out. 04 ] Available from: http://dx.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 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c9sc00094a
  • Source: Chemical Science. Unidade: IFSC

    Subjects: DIFRAÇÃO POR RAIOS X, ESPECTROSCOPIA, SAIS

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      TAO, Xin et al. The special role of B(C6F5)3 in the single electron reduction of quinones by radicals. Chemical Science, v. No 2018, n. 41, p. 8011-8018, 2018Tradução . . Disponível em: http://dx.doi.org/10.1039/c8sc03005g. Acesso em: 04 out. 2022.
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      Tao, X., Daniliuc, C. G., Knitsch, R., Hansen, M. R., Eckert, H., Lübbesmeyer, M., et al. (2018). The special role of B(C6F5)3 in the single electron reduction of quinones by radicals. Chemical Science, No 2018( 41), 8011-8018. doi:10.1039/c8sc03005g
    • NLM

      Tao X, Daniliuc CG, Knitsch R, Hansen MR, Eckert H, Lübbesmeyer M, Studer A, Kehr G, Erker G. The special role of B(C6F5)3 in the single electron reduction of quinones by radicals [Internet]. Chemical Science. 2018 ; No 2018( 41): 8011-8018.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c8sc03005g
    • Vancouver

      Tao X, Daniliuc CG, Knitsch R, Hansen MR, Eckert H, Lübbesmeyer M, Studer A, Kehr G, Erker G. The special role of B(C6F5)3 in the single electron reduction of quinones by radicals [Internet]. Chemical Science. 2018 ; No 2018( 41): 8011-8018.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c8sc03005g
  • Source: Chemical Science. Unidade: IFSC

    Subjects: ESPECTROSCOPIA, RESSONÂNCIA MAGNÉTICA NUCLEAR, DIFRAÇÃO POR RAIOS X

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      WANG, Long et al. Solid state frustrated Lewis pair chemistry. Chemical Science, v. 9, n. 21, p. 4859-4865, 2018Tradução . . Disponível em: http://dx.doi.org/10.1039/c8sc01089g. Acesso em: 04 out. 2022.
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      Wang, L., Kehr, G., Daniliuc, C. G., Brinkköter, M., Wiegand, T., Wübker, A. -L., et al. (2018). Solid state frustrated Lewis pair chemistry. Chemical Science, 9( 21), 4859-4865. doi:10.1039/c8sc01089g
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      Wang L, Kehr G, Daniliuc CG, Brinkköter M, Wiegand T, Wübker A-L, Eckert H, Liu L, Brandenburg JG, Grimme S, Erker G. Solid state frustrated Lewis pair chemistry [Internet]. Chemical Science. 2018 ; 9( 21): 4859-4865.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c8sc01089g
    • Vancouver

      Wang L, Kehr G, Daniliuc CG, Brinkköter M, Wiegand T, Wübker A-L, Eckert H, Liu L, Brandenburg JG, Grimme S, Erker G. Solid state frustrated Lewis pair chemistry [Internet]. Chemical Science. 2018 ; 9( 21): 4859-4865.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c8sc01089g
  • Source: Chemical Science. Unidade: IFSC

    Subjects: ESPECTROSCOPIA, RESSONÂNCIA MAGNÉTICA NUCLEAR, DIFRAÇÃO POR RAIOS X

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      WANG, Long et al. Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical Science, v. 9, n. 6, p. 1544-1550, 2018Tradução . . Disponível em: http://dx.doi.org/10.1039/c7sc04394e. Acesso em: 04 out. 2022.
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      Wang, L., Dong, S., Daniliuc, C. G., Liu, L., Grimme, S., Knitsch, R., et al. (2018). Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical Science, 9( 6), 1544-1550. doi:10.1039/c7sc04394e
    • NLM

      Wang L, Dong S, Daniliuc CG, Liu L, Grimme S, Knitsch R, Eckert H, Hansen MR, Kehr G, Erker G. Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs [Internet]. Chemical Science. 2018 ; 9( 6): 1544-1550.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c7sc04394e
    • Vancouver

      Wang L, Dong S, Daniliuc CG, Liu L, Grimme S, Knitsch R, Eckert H, Hansen MR, Kehr G, Erker G. Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs [Internet]. Chemical Science. 2018 ; 9( 6): 1544-1550.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c7sc04394e
  • 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: http://dx.doi.org/10.1039/c7sc03445h. Acesso em: 04 out. 2022.
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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 2022 out. 04 ] Available from: http://dx.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 2022 out. 04 ] Available from: http://dx.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: http://dx.doi.org/10.1039/c7sc02163a. Acesso em: 04 out. 2022.
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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 2022 out. 04 ] Available from: http://dx.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 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c7sc02163a
  • Source: Chemical Science. Unidade: IQSC

    Subject: 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: http://dx.doi.org/10.1039/c6sc04229e. Acesso em: 04 out. 2022.
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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
    • NLM

      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 2022 out. 04 ] Available from: http://dx.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 2022 out. 04 ] Available from: http://dx.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: http://dx.doi.org/10.1039/c5sc00724k. Acesso em: 04 out. 2022.
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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
    • NLM

      Matuschek D, Eusterwiemann S, Stegemann L, Doerenkamp C, Wibbeling B, Daniliuc CG, Eckert H, Studer A, Doltsinis NL, Strassert CA. Profluorescent verdazyl radicals: synthesis and characterization [Internet]. Chemical Science. 2015 ; 6( 8): 4712-4716.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c5sc00724k
    • Vancouver

      Matuschek D, Eusterwiemann S, Stegemann L, Doerenkamp C, Wibbeling B, Daniliuc CG, Eckert H, Studer A, Doltsinis NL, Strassert CA. Profluorescent verdazyl radicals: synthesis and characterization [Internet]. Chemical Science. 2015 ; 6( 8): 4712-4716.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c5sc00724k
  • Source: Chemical Science. Unidade: IFSC

    Subjects: RESSONÂNCIA MAGNÉTICA, DIFRAÇÃO POR RAIOS X

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      SAJID, Muhammad et al. Reactions of phosphorus/boron frustrated Lewis pairs with SO2. Chemical Science, v. 4, n. Ja 2013, p. 213-219, 2013Tradução . . Disponível em: http://dx.doi.org/10.1039/c2sc21161k. Acesso em: 04 out. 2022.
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      Sajid, M., Eckert, H., Lough, A. J., Fröhlich, R., Daniliuc, C. G., Grimme, S., et al. (2013). Reactions of phosphorus/boron frustrated Lewis pairs with SO2. Chemical Science, 4( Ja 2013), 213-219. doi:10.1039/c2sc21161k
    • NLM

      Sajid M, Eckert H, Lough AJ, Fröhlich R, Daniliuc CG, Grimme S, Stephan DW, Kehr G, Erker G, Klose A, Birkmann B, Liang L, Schirmer B, Wiegand T. Reactions of phosphorus/boron frustrated Lewis pairs with SO2 [Internet]. Chemical Science. 2013 ; 4( Ja 2013): 213-219.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c2sc21161k
    • Vancouver

      Sajid M, Eckert H, Lough AJ, Fröhlich R, Daniliuc CG, Grimme S, Stephan DW, Kehr G, Erker G, Klose A, Birkmann B, Liang L, Schirmer B, Wiegand T. Reactions of phosphorus/boron frustrated Lewis pairs with SO2 [Internet]. Chemical Science. 2013 ; 4( Ja 2013): 213-219.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c2sc21161k
  • Source: Chemical Science. Unidade: IFSC

    Subjects: REAGENTES, RESSONÂNCIA MAGNÉTICA, SPIN

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      EKKERT, Olga et al. Remarkable coordination behavior of alkyl isocyanides toward unsaturated vicinal frustrated P/B Lewis pairs. Chemical Science, v. 4, n. 6, p. 2657-2664, 2013Tradução . . Disponível em: http://dx.doi.org/10.1039/c3sc00082f. Acesso em: 04 out. 2022.
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      Ekkert, O., Miera, G. G., Wiegand, T., Eckert, H., Schirmer, B., Petersen, J. L., et al. (2013). Remarkable coordination behavior of alkyl isocyanides toward unsaturated vicinal frustrated P/B Lewis pairs. Chemical Science, 4( 6), 2657-2664. doi:10.1039/c3sc00082f
    • NLM

      Ekkert O, Miera GG, Wiegand T, Eckert H, Schirmer B, Petersen JL, Daniliuc CG, Fröhlich R, Grimme S, Kehr G, Erker G. Remarkable coordination behavior of alkyl isocyanides toward unsaturated vicinal frustrated P/B Lewis pairs [Internet]. Chemical Science. 2013 ; 4( 6): 2657-2664.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c3sc00082f
    • Vancouver

      Ekkert O, Miera GG, Wiegand T, Eckert H, Schirmer B, Petersen JL, Daniliuc CG, Fröhlich R, Grimme S, Kehr G, Erker G. Remarkable coordination behavior of alkyl isocyanides toward unsaturated vicinal frustrated P/B Lewis pairs [Internet]. Chemical Science. 2013 ; 4( 6): 2657-2664.[citado 2022 out. 04 ] Available from: http://dx.doi.org/10.1039/c3sc00082f
  • Source: Chemical Science. Unidade: IQSC

    Subject: 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: http://dx.doi.org/10.1039/c2sc20490h. Acesso em: 04 out. 2022.
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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
    • NLM

      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 2022 out. 04 ] Available from: http://dx.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 2022 out. 04 ] Available from: http://dx.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 . . Acesso em: 04 out. 2022.
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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
    • NLM

      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. Chemical Science. 2010 ;( 4): 507-514.[citado 2022 out. 04 ]
    • 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. Chemical Science. 2010 ;( 4): 507-514.[citado 2022 out. 04 ]

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