Filtros : "Tetrahedron" Limpar

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  • Source: Tetrahedron. Unidade: IQSC

    Subjects: CATÁLISE, COBRE

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      FURNIEL, Lucas Giani; BURTOLOSO, Antonio Carlos Bender. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron, Oxford, Elsevier, 2020. Disponível em: < https://doi.org/10.1016/j.tet.2020.131313 > DOI: 10.1016/j.tet.2020.131313.
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      Furniel, L. G., & Burtoloso, A. C. B. (2020). Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron. doi:10.1016/j.tet.2020.131313
    • NLM

      Furniel LG, Burtoloso ACB. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides [Internet]. Tetrahedron. 2020 ;Available from: https://doi.org/10.1016/j.tet.2020.131313
    • Vancouver

      Furniel LG, Burtoloso ACB. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides [Internet]. Tetrahedron. 2020 ;Available from: https://doi.org/10.1016/j.tet.2020.131313
  • Source: Tetrahedron. Unidade: IQSC

    Subjects: ALCALOIDES, QUÍMICA

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      PERECIM, Givago P.; DEFLON, Victor Marcelo; MARTINS, Gabriel R.; et al. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, Oxford, Elsevier, v. 76. 131461 July 2020, 2020. Disponível em: < https://doi.org/10.1016/j.tet.2020.131461 > DOI: 10.1016/j.tet.2020.131461.
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      Perecim, G. P., Deflon, V. M., Martins, G. R., Pinto, L. M. C., Casagrande, G. A., Raminelli, C., & Silva, D. O. (2020). Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, 76. 131461 July 2020. doi:10.1016/j.tet.2020.131461
    • NLM

      Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Raminelli C, Silva DO. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020Available from: https://doi.org/10.1016/j.tet.2020.131461
    • Vancouver

      Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Raminelli C, Silva DO. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020Available from: https://doi.org/10.1016/j.tet.2020.131461
  • Source: Tetrahedron. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      VASCONCELOS, Stanley N. S; REIS, Joel S; OLIVEIRA, Isadora M. de; BALFOUR, Michael N; STEFANI, Hélio Alexandre. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, Oxford, v. 75, p. 1865-1959, 2019. Disponível em: < http://dx.doi.org/10.1016/j.tet.2019.02.001 > DOI: 10.1016/j.tet.2019.02.001.
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      Vasconcelos, S. N. S., Reis, J. S., Oliveira, I. M. de, Balfour, M. N., & Stefani, H. A. (2019). Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, 75, 1865-1959. doi:10.1016/j.tet.2019.02.001
    • NLM

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.Available from: http://dx.doi.org/10.1016/j.tet.2019.02.001
    • Vancouver

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.Available from: http://dx.doi.org/10.1016/j.tet.2019.02.001
  • Source: Tetrahedron. Unidades: FCFRP, FFCLRP

    Subjects: AMIDO, MAGNÉSIO, ZINCO, SÍNTESE QUÍMICA, FÁRMACOS, PRODUTOS NATURAIS

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      NISHIMURA, Rodolfo Hideki Vicente; VAZ, Artur de Lara Lima; BOZZINI, Leandro Alves; MURIE, Valter Eduardo; CLOSOSKI, Giuliano Cesar. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets. Tetrahedron, Oxford, v. 75, n. 4, p. 464-474, 2019. Disponível em: < https://doi.org/10.1016/j.tet.2018.12.018 > DOI: 10.1016/j.tet.2018.12.018.
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      Nishimura, R. H. V., Vaz, A. de L. L., Bozzini, L. A., Murie, V. E., & Clososki, G. C. (2019). Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets. Tetrahedron, 75( 4), 464-474. doi:10.1016/j.tet.2018.12.018
    • NLM

      Nishimura RHV, Vaz A de LL, Bozzini LA, Murie VE, Clososki GC. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets [Internet]. Tetrahedron. 2019 ; 75( 4): 464-474.Available from: https://doi.org/10.1016/j.tet.2018.12.018
    • Vancouver

      Nishimura RHV, Vaz A de LL, Bozzini LA, Murie VE, Clososki GC. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets [Internet]. Tetrahedron. 2019 ; 75( 4): 464-474.Available from: https://doi.org/10.1016/j.tet.2018.12.018
  • Source: Tetrahedron. Unidade: IFSC

    Subjects: BIOQUÍMICA, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS

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      MARTELLI, Lorena S. R.; VIEIRA, Lucas C. C.; PAIXÃO, Márcio W.; et al. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity. Tetrahedron, Oxford, Elsevier, v. 75, n. 25, p. 3530-3542, 2019. Disponível em: < http://dx.doi.org/10.1016/j.tet.2019.05.022 > DOI: 10.1016/j.tet.2019.05.022.
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      Martelli, L. S. R., Vieira, L. C. C., Paixão, M. W., Zukerman-Schpector, J., Souza, J. O., Aguiar, A. C. C., et al. (2019). Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity. Tetrahedron, 75( 25), 3530-3542. doi:10.1016/j.tet.2019.05.022
    • NLM

      Martelli LSR, Vieira LCC, Paixão MW, Zukerman-Schpector J, Souza JO, Aguiar ACC, Oliva G, Guido RVC, Corrêa AG. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity [Internet]. Tetrahedron. 2019 ; 75( 25): 3530-3542.Available from: http://dx.doi.org/10.1016/j.tet.2019.05.022
    • Vancouver

      Martelli LSR, Vieira LCC, Paixão MW, Zukerman-Schpector J, Souza JO, Aguiar ACC, Oliva G, Guido RVC, Corrêa AG. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity [Internet]. Tetrahedron. 2019 ; 75( 25): 3530-3542.Available from: http://dx.doi.org/10.1016/j.tet.2019.05.022
  • Source: Tetrahedron. Unidades: IQ, FCF

    Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS

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      REIS, Joel S; FERNANDES, Arthur Bonfá; DÖRR, Barbara Coelho de Freitas; BASTOS, Erick Leite; STEFANI, Hélio Alexandre. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, Oxford, v. 74, p. 6866-6872, 2018. Disponível em: < http://dx.doi.org/10.1016/j.tet.2018.10.019 > DOI: 10.1016/j.tet.2018.10.019.
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      Reis, J. S., Fernandes, A. B., Dörr, B. C. de F., Bastos, E. L., & Stefani, H. A. (2018). Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, 74, 6866-6872. doi:10.1016/j.tet.2018.10.019
    • NLM

      Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.Available from: http://dx.doi.org/10.1016/j.tet.2018.10.019
    • Vancouver

      Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.Available from: http://dx.doi.org/10.1016/j.tet.2018.10.019
  • Source: Tetrahedron. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      DIAS, Rafael Mafra de Paula; MOMO, Patrícia Betoni; BURTOLOSO, Antonio Carlos Bender. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, Oxford, v. 73, n. 26, p. 3720 - 3729, 2017. Disponível em: < http://dx.doi.org/10.1016/j.tet.2017.05.040 > DOI: 10.1016/j.tet.2017.05.040.
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      Dias, R. M. de P., Momo, P. B., & Burtoloso, A. C. B. (2017). One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, 73( 26), 3720 - 3729. doi:10.1016/j.tet.2017.05.040
    • NLM

      Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.Available from: http://dx.doi.org/10.1016/j.tet.2017.05.040
    • Vancouver

      Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.Available from: http://dx.doi.org/10.1016/j.tet.2017.05.040
  • Source: Tetrahedron. Unidade: IQSC

    Assunto: QUÍMICA VERDE

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      LIMA, Rafaely Nascimento; PORTO, André Luiz Meleiro. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, Oxford, v. 58, n. 9, p. 825-828, 2017. Disponível em: < http://dx.doi.org/10.1016/j.tetlet.2016.12.062 > DOI: 10.1016/j.tetlet.2016.12.062.
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      Lima, R. N., & Porto, A. L. M. (2017). Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, 58( 9), 825-828. doi:10.1016/j.tetlet.2016.12.062
    • NLM

      Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.Available from: http://dx.doi.org/10.1016/j.tetlet.2016.12.062
    • Vancouver

      Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.Available from: http://dx.doi.org/10.1016/j.tetlet.2016.12.062
  • Source: Tetrahedron. Unidade: IQSC

    Subjects: FUNGOS, QUÍMICA ORGÂNICA

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      JIMENEZ, David Esteban Quintero; FERREIRA , Irlon Maciel; BIROLLI, Willian Garcia; FONSECA, Luis P.; PORTO, Andre Luiz Meleiro. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, Oxford, v. 72, n. 46, p. 7317-7322, 2016. Disponível em: < http://dx.doi.org/10.1016/j.tet.2016.02.014 > DOI: 10.1016/j.tet.2016.02.014.
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      Jimenez, D. E. Q., Ferreira , I. M., Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2016). Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, 72( 46), 7317-7322. doi:10.1016/j.tet.2016.02.014
    • NLM

      Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.Available from: http://dx.doi.org/10.1016/j.tet.2016.02.014
    • Vancouver

      Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.Available from: http://dx.doi.org/10.1016/j.tet.2016.02.014
  • Source: Tetrahedron. Unidade: IQ

    Subjects: FOTOQUÍMICA, RADIAÇÃO ULTRAVIOLETA

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      COSTA, Damien; GALVÃO, Adelino M; DI PAOLO, Roberto E; et al. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation. Tetrahedron, Hoboken, v. 71, n. 20, p. 3157-3162, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tet.2014.06.092 > DOI: 10.1016/j.tet.2014.06.092.
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      Costa, D., Galvão, A. M., Di Paolo, R. E., Freitas, A. A. de, Lima, J. C., Quina, F. H., & Maçanita, A. L. (2015). Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation. Tetrahedron, 71( 20), 3157-3162. doi:10.1016/j.tet.2014.06.092
    • NLM

      Costa D, Galvão AM, Di Paolo RE, Freitas AA de, Lima JC, Quina FH, Maçanita AL. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation [Internet]. Tetrahedron. 2015 ; 71( 20): 3157-3162.Available from: http://dx.doi.org/10.1016/j.tet.2014.06.092
    • Vancouver

      Costa D, Galvão AM, Di Paolo RE, Freitas AA de, Lima JC, Quina FH, Maçanita AL. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation [Internet]. Tetrahedron. 2015 ; 71( 20): 3157-3162.Available from: http://dx.doi.org/10.1016/j.tet.2014.06.092
  • Source: Tetrahedron. Unidades: FCFRP, FMRP

    Subjects: TRIPANOSSOMICIDAS, TRYPANOSOMA CRUZI, MACRÓFAGOS

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      CAMPO, Vanessa Leiria; IVANOVA, Irina M.; CARVALHO, Ivone; et al. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, Kidlington, v. 71, n. 39, p. 7344–7353, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tet.2015.04.085 > DOI: 10.1016/j.tet.2015.04.085.
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      Campo, V. L., Ivanova, I. M., Carvalho, I., Lopes, C. D., Carneiro, Z., Saalbach, G., et al. (2015). Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, 71( 39), 7344–7353. doi:10.1016/j.tet.2015.04.085
    • NLM

      Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.Available from: http://dx.doi.org/10.1016/j.tet.2015.04.085
    • Vancouver

      Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.Available from: http://dx.doi.org/10.1016/j.tet.2015.04.085
  • Source: Tetrahedron. Unidade: IQ

    Subjects: LEISHMANIA, TERAPIA FOTODINÂMICA

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      SILVA, Alexandre Vieira; LOPEZ SANCHEZ, Almudena; JUNQUEIRA, Helena Couto; et al. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites. Tetrahedron, Oxford, v. 71, n. 3, p. 457-462, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tet.2014.11.072 > DOI: 10.1016/j.tet.2014.11.072.
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      Silva, A. V., Lopez Sanchez, A., Junqueira, H. C., Rivas, L., Baptista, M. da S., & Orellana, G. (2015). Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites. Tetrahedron, 71( 3), 457-462. doi:10.1016/j.tet.2014.11.072
    • NLM

      Silva AV, Lopez Sanchez A, Junqueira HC, Rivas L, Baptista M da S, Orellana G. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites [Internet]. Tetrahedron. 2015 ; 71( 3): 457-462.Available from: http://dx.doi.org/10.1016/j.tet.2014.11.072
    • Vancouver

      Silva AV, Lopez Sanchez A, Junqueira HC, Rivas L, Baptista M da S, Orellana G. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites [Internet]. Tetrahedron. 2015 ; 71( 3): 457-462.Available from: http://dx.doi.org/10.1016/j.tet.2014.11.072
  • Source: Tetrahedron. Unidade: IQ

    Subjects: PALÁDIO, HIDROGENAÇÃO

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      SILVA, Fernanda Parra da; ROSSI, Liane Marcia. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds. Tetrahedron, Oxford, v. 70, n. 20, p. 3314-3318, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2013.10.051 > DOI: 10.1016/j.tet.2013.10.051.
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      Silva, F. P. da, & Rossi, L. M. (2014). Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds. Tetrahedron, 70( 20), 3314-3318. doi:10.1016/j.tet.2013.10.051
    • NLM

      Silva FP da, Rossi LM. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds [Internet]. Tetrahedron. 2014 ; 70( 20): 3314-3318.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.051
    • Vancouver

      Silva FP da, Rossi LM. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds [Internet]. Tetrahedron. 2014 ; 70( 20): 3314-3318.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.051
  • Source: Tetrahedron. Unidade: IQ

    Assunto: BIOGRAFIAS

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      SANTOS, Alcindo Aparecido dos. Professor Alcindo A. dos Santos (Biography). Tetrahedron[S.l: s.n.], 2014.Disponível em: DOI: 10.1016/j.tet.2014.03.077.
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      Santos, A. A. dos. (2014). Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford. doi:10.1016/j.tet.2014.03.077
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      Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.Available from: http://dx.doi.org/10.1016/j.tet.2014.03.077
    • Vancouver

      Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.Available from: http://dx.doi.org/10.1016/j.tet.2014.03.077
  • Source: Tetrahedron. Unidade: IQ

    Subjects: CATALASE, SOLVENTE

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      DONATONI, Maria C; JUNIOR, Gilmar A. B; OLIVEIRA, Kleber T. de; et al. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica. Tetrahedron, Oxford, v. 70, n. 20, p. 3231-3238, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2014.02.017 > DOI: 10.1016/j.tet.2014.02.017.
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      Donatoni, M. C., Junior, G. A. B., Oliveira, K. T. de, Ando, R. A., Brocksom, T. J., & Santos, A. A. dos. (2014). Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica. Tetrahedron, 70( 20), 3231-3238. doi:10.1016/j.tet.2014.02.017
    • NLM

      Donatoni MC, Junior GAB, Oliveira KT de, Ando RA, Brocksom TJ, Santos AA dos. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica [Internet]. Tetrahedron. 2014 ; 70( 20): 3231-3238.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.017
    • Vancouver

      Donatoni MC, Junior GAB, Oliveira KT de, Ando RA, Brocksom TJ, Santos AA dos. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica [Internet]. Tetrahedron. 2014 ; 70( 20): 3231-3238.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.017
  • Source: Tetrahedron. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      BERNARDIM, Barbara; BURTOLOSO, Antonio Carlos Bender. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, Oxford, v. 70, p. 3291-3296, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2013.10.059 > DOI: 10.1016/j.tet.2013.10.059.
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      Bernardim, B., & Burtoloso, A. C. B. (2014). A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, 70, 3291-3296. doi:10.1016/j.tet.2013.10.059
    • NLM

      Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.059
    • Vancouver

      Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.059
  • Source: Tetrahedron. Unidade: FCF

    Subjects: ITÉRBIO, SÍNTESE ORGÂNICA

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    • ABNT

      STEFANI, Hélio Alexandre; MANARIN, Flávia; SOUSA, Ariane C.S; SOUZA, Frederico B; FERRAZ, Witor Ribeiro. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, Oxford, v. 70, n. 20, p. 3243-3248, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2013.11.107 > DOI: 10.1016/j.tet.2013.11.107.
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      Stefani, H. A., Manarin, F., Sousa, A. C. S., Souza, F. B., & Ferraz, W. R. (2014). Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, 70( 20), 3243-3248. doi:10.1016/j.tet.2013.11.107
    • NLM

      Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.Available from: http://dx.doi.org/10.1016/j.tet.2013.11.107
    • Vancouver

      Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.Available from: http://dx.doi.org/10.1016/j.tet.2013.11.107
  • Source: Tetrahedron. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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      SANTOS, Alcindo Aparecido dos. Applied organic synthesis in action [Preface]: strategies and process development. Tetrahedron[S.l: s.n.], 2014.Disponível em: DOI: 10.1016/j.tet.2014.02.053.
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      Santos, A. A. dos. (2014). Applied organic synthesis in action [Preface]: strategies and process development. Tetrahedron. Oxford. doi:10.1016/j.tet.2014.02.053
    • NLM

      Santos AA dos. Applied organic synthesis in action [Preface]: strategies and process development [Internet]. Tetrahedron. 2014 ; 70 3230.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.053
    • Vancouver

      Santos AA dos. Applied organic synthesis in action [Preface]: strategies and process development [Internet]. Tetrahedron. 2014 ; 70 3230.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.053
  • Source: Tetrahedron. Unidade: IQ

    Subjects: SELÊNIO, LIPASE

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      BRONDANI, Patricia Bulegon; GUILMOTO, Nathalie Mariana Andrade de França; DUDEK, Hanna M; FRAAIJE, Marco W; ANDRADE, Leandro Helgueira. Chemoenzymatic approaches to obtain chiral-centered selenium compounds. Tetrahedron, Oxford, v. 68, n. 51, p. 10431-10436, 2012. Disponível em: < http://dx.doi.org/10.1016/j.tet.2012.09.087 > DOI: 10.1016/j.tet.2012.09.087.
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      Brondani, P. B., Guilmoto, N. M. A. de F., Dudek, H. M., Fraaije, M. W., & Andrade, L. H. (2012). Chemoenzymatic approaches to obtain chiral-centered selenium compounds. Tetrahedron, 68( 51), 10431-10436. doi:10.1016/j.tet.2012.09.087
    • NLM

      Brondani PB, Guilmoto NMA de F, Dudek HM, Fraaije MW, Andrade LH. Chemoenzymatic approaches to obtain chiral-centered selenium compounds [Internet]. Tetrahedron. 2012 ; 68( 51): 10431-10436.Available from: http://dx.doi.org/10.1016/j.tet.2012.09.087
    • Vancouver

      Brondani PB, Guilmoto NMA de F, Dudek HM, Fraaije MW, Andrade LH. Chemoenzymatic approaches to obtain chiral-centered selenium compounds [Internet]. Tetrahedron. 2012 ; 68( 51): 10431-10436.Available from: http://dx.doi.org/10.1016/j.tet.2012.09.087
  • Source: Tetrahedron. Unidade: IQ

    Subjects: COMPOSTOS ORGANOMETÁLICOS, CALCOGÊNIOS

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    • ABNT

      SOUSA, Bruno Artur de; KEPPLER, Arthur Franz; GARIANI, Rogério Aparecido; COMASSETO, João Valdir; SANTOS, Alcindo Aparecido dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, Oxford, v. 68, n. 51, p. 10406-10413, 2012. Disponível em: < http://dx.doi.org/10.1016/j.tet.2012.09.027 > DOI: 10.1016/j.tet.2012.09.027.
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      Sousa, B. A. de, Keppler, A. F., Gariani, R. A., Comasseto, J. V., & Santos, A. A. dos. (2012). Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, 68( 51), 10406-10413. doi:10.1016/j.tet.2012.09.027
    • NLM

      Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.Available from: http://dx.doi.org/10.1016/j.tet.2012.09.027
    • Vancouver

      Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.Available from: http://dx.doi.org/10.1016/j.tet.2012.09.027

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