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  • Source: Dalton Transactions. Unidade: IQ

    Subjects: COLORIMETRIA, LUMINESCÊNCIA

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      GONÇALVES, A. C et al. The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes. Dalton Transactions, v. 45, n. 23, p. 9513-9522 : + supplementary materials (S1-S13), 2016Tradução . . Disponível em: https://doi.org/10.1039/c6dt01180b. Acesso em: 06 nov. 2024.
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      Gonçalves, A. C., Pila, V., Oliveira, E., Santos, S. M., J. L. Capelo,, Santos, A. A. dos, & Lodeiro, C. (2016). The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes. Dalton Transactions, 45( 23), 9513-9522 : + supplementary materials (S1-S13). doi:10.1039/c6dt01180b
    • NLM

      Gonçalves AC, Pila V, Oliveira E, Santos SM, J. L. Capelo, Santos AA dos, Lodeiro C. The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes [Internet]. Dalton Transactions. 2016 ; 45( 23): 9513-9522 : + supplementary materials (S1-S13).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/c6dt01180b
    • Vancouver

      Gonçalves AC, Pila V, Oliveira E, Santos SM, J. L. Capelo, Santos AA dos, Lodeiro C. The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes [Internet]. Dalton Transactions. 2016 ; 45( 23): 9513-9522 : + supplementary materials (S1-S13).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/c6dt01180b
  • Source: Tetrahedrom Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, COMPOSTOS ORGÂNICOS

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      AVILA, Thais C et al. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, v. 57, p. 2152-2157, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.03.109. Acesso em: 06 nov. 2024.
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      Avila, T. C., Reginato, M. M., Di Vitta, C., Ducati, L. C., Andrade, L. H., & Marzorati, L. (2016). On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, 57, 2152-2157. doi:10.1016/j.tetlet.2016.03.109
    • NLM

      Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109
    • Vancouver

      Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109
  • Source: Phytochemistry Reviews. Unidade: IQ

    Subjects: PRODUTOS NATURAIS, MAGNOLIALES, METABÓLITOS SECUNDÁRIOS

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      GUTIERREZ, Yasmin Valero et al. Natural products from Peperomia: occurrence, biogenesis and bioactivity. Phytochemistry Reviews, p. 1-25, 2016Tradução . . Disponível em: https://doi.org/10.1007/s11101-016-9461-5. Acesso em: 06 nov. 2024.
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      Gutierrez, Y. V., Yamaguchi, L. F., Moraes, M. M. de, Jeffrey, C. S., & Kato, M. J. (2016). Natural products from Peperomia: occurrence, biogenesis and bioactivity. Phytochemistry Reviews, 1-25. doi:10.1007/s11101-016-9461-5
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      Gutierrez YV, Yamaguchi LF, Moraes MM de, Jeffrey CS, Kato MJ. Natural products from Peperomia: occurrence, biogenesis and bioactivity [Internet]. Phytochemistry Reviews. 2016 ; 1-25.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1007/s11101-016-9461-5
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      Gutierrez YV, Yamaguchi LF, Moraes MM de, Jeffrey CS, Kato MJ. Natural products from Peperomia: occurrence, biogenesis and bioactivity [Internet]. Phytochemistry Reviews. 2016 ; 1-25.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1007/s11101-016-9461-5
  • Source: Organometallics. Unidade: IQ

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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      GUEST, Daniel et al. (N-Heterocyclic Carbene)-palladate complexes in anionic mizoroki− heck coupling cycles: a combined experimental and computational study. Organometallics, v. 34, p. 2463-2470, 2015Tradução . . Disponível em: https://doi.org/10.1021/om5012038. Acesso em: 06 nov. 2024.
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      Guest, D., Silva, V. H. M. da, Batista, A. P. de L., Roe, S. M., Braga, A. A. C., & Navarro, O. (2015). (N-Heterocyclic Carbene)-palladate complexes in anionic mizoroki− heck coupling cycles: a combined experimental and computational study. Organometallics, 34, 2463-2470. doi:10.1021/om5012038
    • NLM

      Guest D, Silva VHM da, Batista AP de L, Roe SM, Braga AAC, Navarro O. (N-Heterocyclic Carbene)-palladate complexes in anionic mizoroki− heck coupling cycles: a combined experimental and computational study [Internet]. Organometallics. 2015 ; 34 2463-2470.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/om5012038
    • Vancouver

      Guest D, Silva VHM da, Batista AP de L, Roe SM, Braga AAC, Navarro O. (N-Heterocyclic Carbene)-palladate complexes in anionic mizoroki− heck coupling cycles: a combined experimental and computational study [Internet]. Organometallics. 2015 ; 34 2463-2470.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/om5012038
  • Source: Analytical Chemistry Research. Unidade: IQ

    Subjects: ESPECTROSCOPIA, MANGANÊS, POTÁSSIO

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      SILVESTRE, Daniel Menezes et al. Feasibility study of calibration strategy for direct quantitative measurement of K and Mg in plant material by laser-induced breakdown spectrometry. Analytical Chemistry Research, v. 5, p. 28-33, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ancr.2015.06.003. Acesso em: 06 nov. 2024.
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      Silvestre, D. M., Barbosa, F. M., Aguiar, B. T., Leme, F. de O., & Nomura, C. S. (2015). Feasibility study of calibration strategy for direct quantitative measurement of K and Mg in plant material by laser-induced breakdown spectrometry. Analytical Chemistry Research, 5, 28-33. doi:10.1016/j.ancr.2015.06.003
    • NLM

      Silvestre DM, Barbosa FM, Aguiar BT, Leme F de O, Nomura CS. Feasibility study of calibration strategy for direct quantitative measurement of K and Mg in plant material by laser-induced breakdown spectrometry [Internet]. Analytical Chemistry Research. 2015 ; 5 28-33.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ancr.2015.06.003
    • Vancouver

      Silvestre DM, Barbosa FM, Aguiar BT, Leme F de O, Nomura CS. Feasibility study of calibration strategy for direct quantitative measurement of K and Mg in plant material by laser-induced breakdown spectrometry [Internet]. Analytical Chemistry Research. 2015 ; 5 28-33.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ancr.2015.06.003
  • Source: Journal of Essential Oil Research. Unidade: IQ

    Subjects: COMPOSTOS VOLÁTEIS, COMPOSITAE

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      NASCIMENTO, Anderson Luis do et al. Chemical characterization of the volatile compounds of the flowers of Bidens segetum Martius ex Colla (Asteraceae). Journal of Essential Oil Research, v. 27, n. 1, p. 70-75, 2015Tradução . . Disponível em: https://doi.org/10.1080/10412905.2014.956819. Acesso em: 06 nov. 2024.
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      Nascimento, A. L. do, Raggi, L., Young, M. C. M., & Moreno, P. R. H. (2015). Chemical characterization of the volatile compounds of the flowers of Bidens segetum Martius ex Colla (Asteraceae). Journal of Essential Oil Research, 27( 1), 70-75. doi:10.1080/10412905.2014.956819
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      Nascimento AL do, Raggi L, Young MCM, Moreno PRH. Chemical characterization of the volatile compounds of the flowers of Bidens segetum Martius ex Colla (Asteraceae) [Internet]. Journal of Essential Oil Research. 2015 ; 27( 1): 70-75.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/10412905.2014.956819
    • Vancouver

      Nascimento AL do, Raggi L, Young MCM, Moreno PRH. Chemical characterization of the volatile compounds of the flowers of Bidens segetum Martius ex Colla (Asteraceae) [Internet]. Journal of Essential Oil Research. 2015 ; 27( 1): 70-75.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/10412905.2014.956819
  • Source: Journal of Mass Spectrometry. Unidade: IQ

    Subjects: ESPECTROMETRIA DE MASSAS, ANTIBIÓTICOS

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      QÌAN, Jìan Qiu et al. Differentiation of Cefaclor and its delta-3 isomer by electrospray mass spectrometry, infrared multiple photon dissociation spectroscopy and theoretical calculations. Journal of Mass Spectrometry, v. 50, n. 1, p. 265-269, 2015Tradução . . Disponível em: https://doi.org/10.1002/jms.3510. Acesso em: 06 nov. 2024.
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      Qìan, J. Q., Correra, T. C., Li, J., Maitre, P., Song, D. Q., & Hu, C. Q. (2015). Differentiation of Cefaclor and its delta-3 isomer by electrospray mass spectrometry, infrared multiple photon dissociation spectroscopy and theoretical calculations. Journal of Mass Spectrometry, 50( 1), 265-269. doi:10.1002/jms.3510
    • NLM

      Qìan JQ, Correra TC, Li J, Maitre P, Song DQ, Hu CQ. Differentiation of Cefaclor and its delta-3 isomer by electrospray mass spectrometry, infrared multiple photon dissociation spectroscopy and theoretical calculations [Internet]. Journal of Mass Spectrometry. 2015 ; 50( 1): 265-269.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/jms.3510
    • Vancouver

      Qìan JQ, Correra TC, Li J, Maitre P, Song DQ, Hu CQ. Differentiation of Cefaclor and its delta-3 isomer by electrospray mass spectrometry, infrared multiple photon dissociation spectroscopy and theoretical calculations [Internet]. Journal of Mass Spectrometry. 2015 ; 50( 1): 265-269.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/jms.3510
  • Source: Abstracts Book. Conference titles: Congress of the International Union for Biochemistry and Molecular Biology - IUBMB. Unidades: IQ, IB

    Subjects: PLASMODIUM, ANTIMALÁRICOS

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      NAKABASHI, Myna et al. Evaluation of amides from Piper as antimalarial compounds. 2015, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq), 2015. . Acesso em: 06 nov. 2024.
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      Nakabashi, M., Yamaguchi, L. F., Fokoue, H. H., Marques, J. V., Kato, M. J., & Garcia, C. R. da S. (2015). Evaluation of amides from Piper as antimalarial compounds. In Abstracts Book. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq).
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      Nakabashi M, Yamaguchi LF, Fokoue HH, Marques JV, Kato MJ, Garcia CR da S. Evaluation of amides from Piper as antimalarial compounds. Abstracts Book. 2015 ;[citado 2024 nov. 06 ]
    • Vancouver

      Nakabashi M, Yamaguchi LF, Fokoue HH, Marques JV, Kato MJ, Garcia CR da S. Evaluation of amides from Piper as antimalarial compounds. Abstracts Book. 2015 ;[citado 2024 nov. 06 ]
  • Source: Advances in Condensed Matter Physics. Unidade: IQ

    Subjects: CALORÍMETROS, LIPÍDEOS

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      PÉREZ, Patrícia Losada et al. Phase transitions of binary lipid mixtures: a combined study by adiabatic scanning calorimetry and quartz crystal microbalance with dissipation monitoring. Advances in Condensed Matter Physics, v. 2015, p. 1-14, 2015Tradução . . Disponível em: https://doi.org/10.1155/2015/479318. Acesso em: 06 nov. 2024.
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      Pérez, P. L., Mertens, N., Vasconcelos, B. de M., Slenders, E., Leys, J., Peeters, M., et al. (2015). Phase transitions of binary lipid mixtures: a combined study by adiabatic scanning calorimetry and quartz crystal microbalance with dissipation monitoring. Advances in Condensed Matter Physics, 2015, 1-14. doi:10.1155/2015/479318
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      Pérez PL, Mertens N, Vasconcelos B de M, Slenders E, Leys J, Peeters M, van Grinsven B, Gruber J, Glorieux C, Pfeiffer H, Wagner P, Thoen J. Phase transitions of binary lipid mixtures: a combined study by adiabatic scanning calorimetry and quartz crystal microbalance with dissipation monitoring [Internet]. Advances in Condensed Matter Physics. 2015 ; 2015 1-14.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1155/2015/479318
    • Vancouver

      Pérez PL, Mertens N, Vasconcelos B de M, Slenders E, Leys J, Peeters M, van Grinsven B, Gruber J, Glorieux C, Pfeiffer H, Wagner P, Thoen J. Phase transitions of binary lipid mixtures: a combined study by adiabatic scanning calorimetry and quartz crystal microbalance with dissipation monitoring [Internet]. Advances in Condensed Matter Physics. 2015 ; 2015 1-14.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1155/2015/479318
  • Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química/SBQ. Unidade: IQ

    Assunto: REAÇÕES QUÍMICAS

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      SERVILHA, Bruno Moraes e CORREIA, Carlos Roque Duarte e BRAGA, Ataualpa Albert Carmo. Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study. 2015, Anais.. São Paulo: Sociedade Brasileira de Química/SBQ, 2015. Disponível em: http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf. Acesso em: 06 nov. 2024.
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      Servilha, B. M., Correia, C. R. D., & Braga, A. A. C. (2015). Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study. In Resumos. São Paulo: Sociedade Brasileira de Química/SBQ. Recuperado de http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf
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      Servilha BM, Correia CRD, Braga AAC. Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study [Internet]. Resumos. 2015 ;[citado 2024 nov. 06 ] Available from: http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf
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      Servilha BM, Correia CRD, Braga AAC. Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study [Internet]. Resumos. 2015 ;[citado 2024 nov. 06 ] Available from: http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf
  • Source: Dyes and Pigments. Unidade: IQ

    Subjects: FLUORESCÊNCIA, SOLVENTE

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      SANTIN, Luiza R. R et al. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures. Dyes and Pigments, v. 119, p. 12-21, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2015.03.004. Acesso em: 06 nov. 2024.
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      Santin, L. R. R., Santos, S. C. dos, Novo, D. L. R., Bianchini, D., Gerola, A. P., Braga, G., et al. (2015). Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures. Dyes and Pigments, 119, 12-21. doi:10.1016/j.dyepig.2015.03.004
    • NLM

      Santin LRR, Santos SC dos, Novo DLR, Bianchini D, Gerola AP, Braga G, Caetano W, Moreira LM, Bastos EL, Romani AP, Oliveira HPM de. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures [Internet]. Dyes and Pigments. 2015 ; 119 12-21.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
    • Vancouver

      Santin LRR, Santos SC dos, Novo DLR, Bianchini D, Gerola AP, Braga G, Caetano W, Moreira LM, Bastos EL, Romani AP, Oliveira HPM de. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures [Internet]. Dyes and Pigments. 2015 ; 119 12-21.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: BIOLUMINESCÊNCIA, QUÍMICA ORGÂNICA

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      BARTOLONI, Fernando Heering et al. Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects. Journal of Organic Chemistry, v. 80, n. 8, p. 3745-3751, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b00515. Acesso em: 06 nov. 2024.
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      Bartoloni, F. H., Oliveira, M. A. de, Ciscato, L. F. M. L., Augusto, F. A., Bastos, E. L., & Baader, W. J. (2015). Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects. Journal of Organic Chemistry, 80( 8), 3745-3751. doi:10.1021/acs.joc.5b00515
    • NLM

      Bartoloni FH, Oliveira MA de, Ciscato LFML, Augusto FA, Bastos EL, Baader WJ. Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects [Internet]. Journal of Organic Chemistry. 2015 ; 80( 8): 3745-3751.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.joc.5b00515
    • Vancouver

      Bartoloni FH, Oliveira MA de, Ciscato LFML, Augusto FA, Bastos EL, Baader WJ. Chemiluminescence efficiency of catalyzed 1,2-dioxetanone decomposition determined by steric effects [Internet]. Journal of Organic Chemistry. 2015 ; 80( 8): 3745-3751.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.joc.5b00515
  • Source: Photochemical & Photobiological Sciences. Unidade: IQ

    Subjects: BIOLUMINESCÊNCIA, QUÍMICA ORGÂNICA

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      KHALID, Muhammad et al. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems. Photochemical & Photobiological Sciences, v. 14, n. 7, p. 1296-1305, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5pp00152h. Acesso em: 06 nov. 2024.
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      khalid, M., Souza Junior, S. P. de, Ciscato, L. F. M. L., Bartoloni, F. H., & Baader, W. J. (2015). Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems. Photochemical & Photobiological Sciences, 14( 7), 1296-1305. doi:10.1039/c5pp00152h
    • NLM

      khalid M, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems [Internet]. Photochemical & Photobiological Sciences. 2015 ; 14( 7): 1296-1305.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/c5pp00152h
    • Vancouver

      khalid M, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems [Internet]. Photochemical & Photobiological Sciences. 2015 ; 14( 7): 1296-1305.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1039/c5pp00152h
  • Source: Sustainable Catalysis: With Non-endangered Metals, Part 2. Unidade: IQ

    Subjects: TÁLIO, QUÍMICA INORGÂNICA, CATALISADORES

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      CARNEIRO, Vânia Maria Teixeira e LONGO JUNIOR, Luiz Sidney e SILVA JUNIOR, Luiz Fernando da. Thallium-based catalysts. Sustainable Catalysis: With Non-endangered Metals, Part 2. Tradução . Cambridge: Royal Society of Chemistry, 2015. . . Acesso em: 06 nov. 2024.
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      Carneiro, V. M. T., Longo Junior, L. S., & Silva Junior, L. F. da. (2015). Thallium-based catalysts. In Sustainable Catalysis: With Non-endangered Metals, Part 2. Cambridge: Royal Society of Chemistry.
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      Carneiro VMT, Longo Junior LS, Silva Junior LF da. Thallium-based catalysts. In: Sustainable Catalysis: With Non-endangered Metals, Part 2. Cambridge: Royal Society of Chemistry; 2015. [citado 2024 nov. 06 ]
    • Vancouver

      Carneiro VMT, Longo Junior LS, Silva Junior LF da. Thallium-based catalysts. In: Sustainable Catalysis: With Non-endangered Metals, Part 2. Cambridge: Royal Society of Chemistry; 2015. [citado 2024 nov. 06 ]
  • Source: Book of Abstracts. Conference titles: Latin-American Symposium on Biotechnology, Biomedical, Biopharmaceutical, and Industrial Applications of Capillary Electrophoresis and Microchip Technology (LACE). Unidade: IQ

    Assunto: TESTOSTERONA (ANÁLOGOS E DERIVADOS)

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      MORAIS, Maicon de et al. Development of a micellar electrokinetic chromatography (MEKC) method for the simultaneous determination of testosterone derivatives in seized formulations using multi-segment injection, solute identification via quantitative structure-retention relationships (QSRR) and single standard calibration procedures. 2015, Anais.. São Paulo: VLS Print Solution, 2015. . Acesso em: 06 nov. 2024.
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      Morais, M. de, Uezu, N., Picossi, C. R. C., Farah, J. P. S., Demétrio, B. P., Freitas, F. A. de, et al. (2015). Development of a micellar electrokinetic chromatography (MEKC) method for the simultaneous determination of testosterone derivatives in seized formulations using multi-segment injection, solute identification via quantitative structure-retention relationships (QSRR) and single standard calibration procedures. In Book of Abstracts. São Paulo: VLS Print Solution.
    • NLM

      Morais M de, Uezu N, Picossi CRC, Farah JPS, Demétrio BP, Freitas FA de, Zilly A, Tavares MFM. Development of a micellar electrokinetic chromatography (MEKC) method for the simultaneous determination of testosterone derivatives in seized formulations using multi-segment injection, solute identification via quantitative structure-retention relationships (QSRR) and single standard calibration procedures. Book of Abstracts. 2015 ;[citado 2024 nov. 06 ]
    • Vancouver

      Morais M de, Uezu N, Picossi CRC, Farah JPS, Demétrio BP, Freitas FA de, Zilly A, Tavares MFM. Development of a micellar electrokinetic chromatography (MEKC) method for the simultaneous determination of testosterone derivatives in seized formulations using multi-segment injection, solute identification via quantitative structure-retention relationships (QSRR) and single standard calibration procedures. Book of Abstracts. 2015 ;[citado 2024 nov. 06 ]
  • Source: Abstract. Conference titles: Brazilian Conference on Natural Products - BCNP. Unidades: IB, IQ

    Subjects: BOTÂNICA (CLASSIFICAÇÃO), COMPOSITAE, MEDICINA POPULAR, FLAVONÓIDES, PRODUTOS NATURAIS, FITOQUÍMICA, QUÍMICA MÉDICA

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      LOPES, Stephanie F. S et al. Baccharis oxyodonta extracts: antiradical capacity an phenolic compounds. 2015, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2015. Disponível em: http://www.infobibos.com/bcnp/cd/search-in-abstracts.html. Acesso em: 06 nov. 2024.
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      Lopes, S. F. S., Peres, V. O., Fávero, O. A., Ferreira, E. A., Ferreira, M. J. P., Souza, G. A. de, et al. (2015). Baccharis oxyodonta extracts: antiradical capacity an phenolic compounds. In Abstract. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://www.infobibos.com/bcnp/cd/search-in-abstracts.html
    • NLM

      Lopes SFS, Peres VO, Fávero OA, Ferreira EA, Ferreira MJP, Souza GA de, Romoff P, Baader WJ. Baccharis oxyodonta extracts: antiradical capacity an phenolic compounds [Internet]. Abstract. 2015 ;[citado 2024 nov. 06 ] Available from: http://www.infobibos.com/bcnp/cd/search-in-abstracts.html
    • Vancouver

      Lopes SFS, Peres VO, Fávero OA, Ferreira EA, Ferreira MJP, Souza GA de, Romoff P, Baader WJ. Baccharis oxyodonta extracts: antiradical capacity an phenolic compounds [Internet]. Abstract. 2015 ;[citado 2024 nov. 06 ] Available from: http://www.infobibos.com/bcnp/cd/search-in-abstracts.html
  • Source: Comparative Biochemistry and Physiology, Part C. Unidade: IQ

    Subjects: ANURA, PIPIDAE

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      MARIANO, Douglas Oscar Ceolin et al. Pipa carvalhoi skin secretion profiling: absence of peptides and identification of kynurenic acid as the major constitutive component. Comparative Biochemistry and Physiology, Part C, v. 167, p. 1-6, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.cbpc.2014.08.001. Acesso em: 06 nov. 2024.
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      Mariano, D. O. C., Yamaguchi, L. F., Jared, C., Antoniazzi, M. M., Sciani, J. M., Kato, M. J., & Pimenta, D. C. (2015). Pipa carvalhoi skin secretion profiling: absence of peptides and identification of kynurenic acid as the major constitutive component. Comparative Biochemistry and Physiology, Part C, 167, 1-6. doi:10.1016/j.cbpc.2014.08.001
    • NLM

      Mariano DOC, Yamaguchi LF, Jared C, Antoniazzi MM, Sciani JM, Kato MJ, Pimenta DC. Pipa carvalhoi skin secretion profiling: absence of peptides and identification of kynurenic acid as the major constitutive component [Internet]. Comparative Biochemistry and Physiology, Part C. 2015 ; 167 1-6.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.cbpc.2014.08.001
    • Vancouver

      Mariano DOC, Yamaguchi LF, Jared C, Antoniazzi MM, Sciani JM, Kato MJ, Pimenta DC. Pipa carvalhoi skin secretion profiling: absence of peptides and identification of kynurenic acid as the major constitutive component [Internet]. Comparative Biochemistry and Physiology, Part C. 2015 ; 167 1-6.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.cbpc.2014.08.001
  • Source: Biotechnology Advances. Unidades: IQ, IQSC

    Subjects: QUÍMICA, ENZIMAS

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      BIROLLI, Willian Garcia et al. Biocatalysis and biotransformation in Brazil: an overview. Biotechnology Advances, v. 33, p. 481-510, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.biotechadv.2015.02.001. Acesso em: 06 nov. 2024.
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      Birolli, W. G., Ferreira , I. M., Alvarenga, N., Matos, I. L. de, Comasseto, J. V., & Porto, A. L. M. (2015). Biocatalysis and biotransformation in Brazil: an overview. Biotechnology Advances, 33, 481-510. doi:10.1016/j.biotechadv.2015.02.001
    • NLM

      Birolli WG, Ferreira IM, Alvarenga N, Matos IL de, Comasseto JV, Porto ALM. Biocatalysis and biotransformation in Brazil: an overview [Internet]. Biotechnology Advances. 2015 ; 33 481-510.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.biotechadv.2015.02.001
    • Vancouver

      Birolli WG, Ferreira IM, Alvarenga N, Matos IL de, Comasseto JV, Porto ALM. Biocatalysis and biotransformation in Brazil: an overview [Internet]. Biotechnology Advances. 2015 ; 33 481-510.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.biotechadv.2015.02.001
  • Source: Journal of Photochemistry and Photobiology A: Chemistry. Unidade: IQ

    Subjects: VISCOSIDADE DO FLUXO DOS LÍQUIDOS, FOTOQUÍMICA, LUMINESCÊNCIA

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      KHALID, Muhammad et al. Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures. Journal of Photochemistry and Photobiology A: Chemistry, v. 312, p. 81-87, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jphotochem.2015.06.031. Acesso em: 06 nov. 2024.
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      khalid, M., Oliveira, M. A. de, Souza Junior, S. P. de, Ciscato, L. F. M. L., Bartoloni, F. H., & Baader, W. J. (2015). Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures. Journal of Photochemistry and Photobiology A: Chemistry, 312, 81-87. doi:10.1016/j.jphotochem.2015.06.031
    • NLM

      khalid M, Oliveira MA de, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures [Internet]. Journal of Photochemistry and Photobiology A: Chemistry. 2015 ; 312 81-87.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jphotochem.2015.06.031
    • Vancouver

      khalid M, Oliveira MA de, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures [Internet]. Journal of Photochemistry and Photobiology A: Chemistry. 2015 ; 312 81-87.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jphotochem.2015.06.031
  • Source: Journal of Physical Chemistry A. Unidade: IQ

    Subjects: ESPECTROSCOPIA, FÍSICO-QUÍMICA

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      RODRIGUES, Daniel Nopper Silva e DUCATI, Lucas Colucci e DAL COLLE, Maurizio. Conformational analysis and electronic interactions of some 4 '-substituted-2-ethylthio-phenylacetates. Journal of Physical Chemistry A, v. 119, n. 16, p. 3823-3832, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.jpca.5b01531. Acesso em: 06 nov. 2024.
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      Rodrigues, D. N. S., Ducati, L. C., & Dal Colle, M. (2015). Conformational analysis and electronic interactions of some 4 '-substituted-2-ethylthio-phenylacetates. Journal of Physical Chemistry A, 119( 16), 3823-3832. doi:10.1021/acs.jpca.5b01531
    • NLM

      Rodrigues DNS, Ducati LC, Dal Colle M. Conformational analysis and electronic interactions of some 4 '-substituted-2-ethylthio-phenylacetates [Internet]. Journal of Physical Chemistry A. 2015 ; 119( 16): 3823-3832.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jpca.5b01531
    • Vancouver

      Rodrigues DNS, Ducati LC, Dal Colle M. Conformational analysis and electronic interactions of some 4 '-substituted-2-ethylthio-phenylacetates [Internet]. Journal of Physical Chemistry A. 2015 ; 119( 16): 3823-3832.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jpca.5b01531

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