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Artigo de periodico
The three-center two-positron bond (2022)
Charry, Jorge ; Moncada, Felix ; Barborini, Matteo ; Pedraza-González, Laura Milena ; Varella, Márcio Teixeira do Nascimento ; Tkatchenko, Alexandre ; Reyes, Andres
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.
APA
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
Artigo de periodico
Asymmetric transformations from sulfoxonium ylides (2022)
Caiuby, Clarice Alves Dale ; Furniel, Lucas Giani; Burtoloso, Antonio Carlos Bender
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.
APA
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
Artigo de periodico
Cooperative copper-squaramide catalysis for the enantioselective N–H insertion reaction with sulfoxonium ylides (2021)
Furniel, Lucas G.; Perez, Radell Echemendía; Burtoloso, Antonio Carlos Bender
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.
APA
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
Artigo de periodico
Covalent bonds in positron dihalides (2020)
Moncada, Félix; Pedraza-González, Laura; Charry, Jorge; Varella, Márcio Teixeira do Nascimento ; Reyes, Andrés
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
Artigo de periodico
Studying the phosphoryl transfer mechanism of the E. coli phosphofructokinase-2: from X-ray structure to quantum mechanics/molecular mechanics simulations (2019)
Murillo-López, Juliana; Zinovjev, Kirill; Pereira, Humberto d'Muniz; Caniuguir, Andres; Garratt, Richard Charles ; Babul, Jorge; Recabarren, Rodrigo; Alzate-Morales, Jans; Caballero, Julio; Tuñón, Iñaki; Cabrera, Ricardo
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.
APA
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 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
Artigo de periodico
The special role of B(C6F5)3 in the single electron reduction of quinones by radicals (2018)
Tao, Xin; Daniliuc, Constantin G.; Knitsch, Robert; Hansen, Michael Ryan; Eckert, Hellmut ; Lübbesmeyer, Maximilian; Studer, Armido; Kehr, Gerald; Erker, Gerhard
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: https://doi.org/10.1039/c8sc03005g. Acesso em: 13 nov. 2024.
APA
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 2024 nov. 13 ] Available from: https://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 2024 nov. 13 ] Available from: https://doi.org/10.1039/c8sc03005g
Artigo de periodico
Solid state frustrated Lewis pair chemistry (2018)
Wang, Long; Kehr, Gerald; Daniliuc, Constantin G.; Brinkköter, Melanie; Wiegand, Thomas; Wübker, Anna-Lena; Eckert, Hellmut ; Liu, Lei; Brandenburg, Jan Gerit; Grimme, Stefan; Erker, Gerhard
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: https://doi.org/10.1039/c8sc01089g. Acesso em: 13 nov. 2024.
APA
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
NLM
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 2024 nov. 13 ] Available from: https://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 2024 nov. 13 ] Available from: https://doi.org/10.1039/c8sc01089g
Artigo de periodico
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs (2018)
Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut ; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Source: Chemical Science. Unidade: IFSC
Subjects: ESPECTROSCOPIA, RESSONÂNCIA MAGNÉTICA NUCLEAR, DIFRAÇÃO POR RAIOS X
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ABNT
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: https://doi.org/10.1039/c7sc04394e. Acesso em: 13 nov. 2024.
APA
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 2024 nov. 13 ] Available from: https://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 2024 nov. 13 ] Available from: https://doi.org/10.1039/c7sc04394e
Artigo de periodico
One-dimensional diamondoid polyaniline-like nanothreads from compressed crystal aniline (2018)
Nobrega, Marcelo Medre; Teixeira Neto, Érico; Cairns, Andrew B; Temperini, Márcia Laudelina Arruda ; Bini, Roberto
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.
APA
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
Artigo de periodico
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 (2017)
Viesser, Renan V; Ducati, Lucas Colucci ; Tormena, Cláudio F; Autschbach, Jochen
Source: Chemical Science. Unidade: IQ
Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, ORBITAL MOLECULAR
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ABNT
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.
APA
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
Artigo de periodico
Methyltransferase-directed covalent coupling of fluorophores to DNA (2017)
Lauer, Milena Helmer; Vranken, Charlotte; Deen, Jochem; Frederickx, Wout; Vanderline, F. A; Wand, Nathaniel; Leen, Volker; Gehlen, Marcelo Henrique ; Hofkens, Johan; Neely, Robert K
Source: Chemical Science. Unidade: IQSC
Assunto: DNA
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ABNT
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.
APA
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 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
Artigo de periodico
Profluorescent verdazyl radicals: synthesis and characterization (2015)
Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut ; Studer, Armido
Source: Chemical Science. Unidade: IFSC
Subjects: FLUORESCÊNCIA, ESPECTROSCOPIA
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ABNT
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.
APA
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, 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
Artigo de periodico
Remarkable coordination behavior of alkyl isocyanides toward unsaturated vicinal frustrated P/B Lewis pairs (2013)
Ekkert, Olga; Miera, Greco González; Wiegand, Thomas; Eckert, Hellmut ; Schirmer, Birgitta; Petersen, Jeffrey L.; Daniliuc, Constantin G.; Fröhlich, Roland; Grimme, Stefan; Kehr, Gerald; Erker, Gerhard
Source: Chemical Science. Unidade: IFSC
Subjects: REAGENTES, RESSONÂNCIA MAGNÉTICA, SPIN
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ABNT
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: https://doi.org/10.1039/c3sc00082f. Acesso em: 13 nov. 2024.
APA
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 2024 nov. 13 ] Available from: https://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 2024 nov. 13 ] Available from: https://doi.org/10.1039/c3sc00082f
Artigo de periodico
Mechanistic changes observed in heavy water for nitrate reduction reaction on palladium-modified Pt(hkl) electrodes (2012)
Souza-Garcia, Janaina; Ticianelli, Edson Antonio ; Climent, V; Feliu, J. M
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.
APA
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 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
Artigo de periodico
Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase (2010)
Campo, Vanessa L.; Carvalho, Ivone; Silva, Carlos Henrique Tomich de Paula da; Schenkman, Sergio; Hill, Lionel; Nepogodiev, Sergey A.; Field, Robert A.
Source: Chemical Science. Unidade: FCFRP
Subjects: TRYPANOSOMA CRUZI, QUÍMICA FARMACÊUTICA
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ABNT
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.
APA
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 [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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