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  • Source: Journal of Mass Spectrometry. Unidade: FFCLRP

    Subjects: ÍONS, FLAVONOIDES, ESPECTROMETRIA DE MASSAS, QUÍMICA, CIÊNCIA DA COMPUTAÇÃO

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      DIAS, Herbert J et al. Electrospray ionization tandem mass spectrometry of 4‐aryl‐3,4‐dihydrocoumarins. Journal of Mass Spectrometry, v. 59, n. 7, 2024Tradução . . Disponível em: https://doi.org/10.1002/jms.5062. Acesso em: 08 out. 2025.
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      Dias, H. J., Santos, W. H., S. Filho, L. C., Crevelin, E. J., McIndoe, J. S., Vessecchi, R., & Crotti, A. E. M. (2024). Electrospray ionization tandem mass spectrometry of 4‐aryl‐3,4‐dihydrocoumarins. Journal of Mass Spectrometry, 59( 7). doi:10.1002/jms.5062
    • NLM

      Dias HJ, Santos WH, S. Filho LC, Crevelin EJ, McIndoe JS, Vessecchi R, Crotti AEM. Electrospray ionization tandem mass spectrometry of 4‐aryl‐3,4‐dihydrocoumarins [Internet]. Journal of Mass Spectrometry. 2024 ; 59( 7):[citado 2025 out. 08 ] Available from: https://doi.org/10.1002/jms.5062
    • Vancouver

      Dias HJ, Santos WH, S. Filho LC, Crevelin EJ, McIndoe JS, Vessecchi R, Crotti AEM. Electrospray ionization tandem mass spectrometry of 4‐aryl‐3,4‐dihydrocoumarins [Internet]. Journal of Mass Spectrometry. 2024 ; 59( 7):[citado 2025 out. 08 ] Available from: https://doi.org/10.1002/jms.5062
  • Source: Journal of Chemical Information and Modeling. Unidade: FFCLRP

    Subjects: QUÍMICA, REPLICAÇÃO DO DNA, GENÔMICA, ÁCIDOS NUCLEICOS

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      PALERMO, Giulia e SOARES, Thereza A. Editing DNA and RNA through Computations [Editorial]. Journal of Chemical Information and Modeling. Washington: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1021/acs.jcim.3c01824. Acesso em: 08 out. 2025. , 2023
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      Palermo, G., & Soares, T. A. (2023). Editing DNA and RNA through Computations [Editorial]. Journal of Chemical Information and Modeling. Washington: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo. doi:10.1021/acs.jcim.3c01824
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      Palermo G, Soares TA. Editing DNA and RNA through Computations [Editorial] [Internet]. Journal of Chemical Information and Modeling. 2023 ; 63( 24): 7603-7604.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jcim.3c01824
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      Palermo G, Soares TA. Editing DNA and RNA through Computations [Editorial] [Internet]. Journal of Chemical Information and Modeling. 2023 ; 63( 24): 7603-7604.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jcim.3c01824
  • Source: Rapid Communications in Mass Spectrometry. Unidade: FCFRP

    Subjects: ALCALOIDES, FARMACOLOGIA, ANIMAIS, PESOS E MEDIDAS CORPORAIS, RAIZ, PLANTAS, ESPECTROMETRIA DE MASSAS, QUÍMICA

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      GAZOLLA, Matheus Coutinho et al. Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity. Rapid Communications in Mass Spectrometry, v. 34, 2020Tradução . . Disponível em: https://doi.org/10.1002/rcm.8705. Acesso em: 08 out. 2025.
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      Gazolla, M. C., Marques, L. M. M., Silva, M. G. e, Araújo, M. T. M. F., Mendes, R. L., Almeida, J. R. G. da S., et al. (2020). Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity. Rapid Communications in Mass Spectrometry, 34. doi:10.1002/rcm.8705
    • NLM

      Gazolla MC, Marques LMM, Silva MG e, Araújo MTMF, Mendes RL, Almeida JRG da S, Vessecchi R, Lopes NP. Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity [Internet]. Rapid Communications in Mass Spectrometry. 2020 ; 34[citado 2025 out. 08 ] Available from: https://doi.org/10.1002/rcm.8705
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      Gazolla MC, Marques LMM, Silva MG e, Araújo MTMF, Mendes RL, Almeida JRG da S, Vessecchi R, Lopes NP. Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity [Internet]. Rapid Communications in Mass Spectrometry. 2020 ; 34[citado 2025 out. 08 ] Available from: https://doi.org/10.1002/rcm.8705
  • Source: Journal of Natural Products. Unidade: FCFRP

    Subjects: BACTÉRIAS, QUÍMICA, FÁRMACOS, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)

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      FUKUDA, Taise Tomie Hebihara et al. Research tales from the Clardy Laboratory: function-driven natural product discovery. Journal of Natural Products, v. 83, n. 3, p. 744-755, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jnatprod.9b01086. Acesso em: 08 out. 2025.
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      Fukuda, T. T. H., Cassilly, C. D., Gerdt, J. P., Henke, M. T., Helfrich, E. J. N., & Mevers, E. (2020). Research tales from the Clardy Laboratory: function-driven natural product discovery. Journal of Natural Products, 83( 3), 744-755. doi:10.1021/acs.jnatprod.9b01086
    • NLM

      Fukuda TTH, Cassilly CD, Gerdt JP, Henke MT, Helfrich EJN, Mevers E. Research tales from the Clardy Laboratory: function-driven natural product discovery [Internet]. Journal of Natural Products. 2020 ; 83( 3): 744-755.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01086
    • Vancouver

      Fukuda TTH, Cassilly CD, Gerdt JP, Henke MT, Helfrich EJN, Mevers E. Research tales from the Clardy Laboratory: function-driven natural product discovery [Internet]. Journal of Natural Products. 2020 ; 83( 3): 744-755.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01086
  • Source: Journal of Chemical Theory and Computation. Unidade: FCFRP

    Subjects: SIMULAÇÃO, CRISTALOGRAFIA, CONFORMAÇÃO PROTEICA, PROTEÍNAS, QUÍMICA

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      SILVA, Fernando Luís Barroso da e STERPONE, Fabio e DERREUMAUX, Philippe. OPEP6: a new constant-pH molecular dynamics simulation scheme with OPEP coarse-grained force field. Journal of Chemical Theory and Computation, v. 15, n. 6, p. 3875-3888, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.jctc.9b00202. Acesso em: 08 out. 2025.
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      Silva, F. L. B. da, Sterpone, F., & Derreumaux, P. (2019). OPEP6: a new constant-pH molecular dynamics simulation scheme with OPEP coarse-grained force field. Journal of Chemical Theory and Computation, 15( 6), 3875-3888. doi:10.1021/acs.jctc.9b00202
    • NLM

      Silva FLB da, Sterpone F, Derreumaux P. OPEP6: a new constant-pH molecular dynamics simulation scheme with OPEP coarse-grained force field [Internet]. Journal of Chemical Theory and Computation. 2019 ; 15( 6): 3875-3888.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jctc.9b00202
    • Vancouver

      Silva FLB da, Sterpone F, Derreumaux P. OPEP6: a new constant-pH molecular dynamics simulation scheme with OPEP coarse-grained force field [Internet]. Journal of Chemical Theory and Computation. 2019 ; 15( 6): 3875-3888.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jctc.9b00202
  • Source: Journal of Agricultural and Food Chemistry. Unidade: FCFRP

    Subjects: QUÍMICA, CROMATOGRAFIA LÍQUIDA DE ALTA PRESSÃO, SEMENTES, ULTRASSOM

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      ARRUDA, Caroline et al. Development of a validated high-performance liquid chromatography method and optimization of the extraction of lignans from Piper cubeba. Journal of Agricultural and Food Chemistry, v. 67, n. 2, p. 753-759, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.jafc.8b05359. Acesso em: 08 out. 2025.
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      Arruda, C., Mejía, J. A. A., Ribeiro, V. P., Costa Oliveira, L., Silva, M. L. A. e, & Bastos, J. K. (2019). Development of a validated high-performance liquid chromatography method and optimization of the extraction of lignans from Piper cubeba. Journal of Agricultural and Food Chemistry, 67( 2), 753-759. doi:10.1021/acs.jafc.8b05359
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      Arruda C, Mejía JAA, Ribeiro VP, Costa Oliveira L, Silva MLA e, Bastos JK. Development of a validated high-performance liquid chromatography method and optimization of the extraction of lignans from Piper cubeba [Internet]. Journal of Agricultural and Food Chemistry. 2019 ; 67( 2): 753-759.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jafc.8b05359
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      Arruda C, Mejía JAA, Ribeiro VP, Costa Oliveira L, Silva MLA e, Bastos JK. Development of a validated high-performance liquid chromatography method and optimization of the extraction of lignans from Piper cubeba [Internet]. Journal of Agricultural and Food Chemistry. 2019 ; 67( 2): 753-759.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.jafc.8b05359
  • Source: Holzforschung. Unidade: IQSC

    Subjects: QUÍMICA, DIÓXIDO DE CARBONO

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      FRANCISCO, Roberta Pacheco e COLODETTE, Jorge Luiz e CURVELO, Antonio Aprigio da Silva. Hydrogen peroxide and supercritical carbon dioxide: a new bleaching stage for eucalyptus kraft-'O IND.2' pulps. Holzforschung, v. 65, n. 3, p. 303-307, 2011Tradução . . Disponível em: https://doi.org/10.1515/HF.2011.031. Acesso em: 08 out. 2025.
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      Francisco, R. P., Colodette, J. L., & Curvelo, A. A. da S. (2011). Hydrogen peroxide and supercritical carbon dioxide: a new bleaching stage for eucalyptus kraft-'O IND.2' pulps. Holzforschung, 65( 3), 303-307. doi:10.1515/HF.2011.031
    • NLM

      Francisco RP, Colodette JL, Curvelo AA da S. Hydrogen peroxide and supercritical carbon dioxide: a new bleaching stage for eucalyptus kraft-'O IND.2' pulps [Internet]. Holzforschung. 2011 ; 65( 3): 303-307.[citado 2025 out. 08 ] Available from: https://doi.org/10.1515/HF.2011.031
    • Vancouver

      Francisco RP, Colodette JL, Curvelo AA da S. Hydrogen peroxide and supercritical carbon dioxide: a new bleaching stage for eucalyptus kraft-'O IND.2' pulps [Internet]. Holzforschung. 2011 ; 65( 3): 303-307.[citado 2025 out. 08 ] Available from: https://doi.org/10.1515/HF.2011.031
  • Source: Journal of Physical Chemistry B. Unidade: FFCLRP

    Subjects: QUÍMICA, PROTEÍNAS

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      MONTEIRO, Douglas Santos e NOBRE, Thatyane Morimoto e ZANIQUELLI, Maria Elisabete Darbello. Hyaluronidase behavior at the air/liquid and air/lipid interfaces and improved enzymatic activity by its immobilization in a biomembrane model. Journal of Physical Chemistry B, v. 115, n. 16, p. 4801-4809, 2011Tradução . . Acesso em: 08 out. 2025.
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      Monteiro, D. S., Nobre, T. M., & Zaniquelli, M. E. D. (2011). Hyaluronidase behavior at the air/liquid and air/lipid interfaces and improved enzymatic activity by its immobilization in a biomembrane model. Journal of Physical Chemistry B, 115( 16), 4801-4809.
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      Monteiro DS, Nobre TM, Zaniquelli MED. Hyaluronidase behavior at the air/liquid and air/lipid interfaces and improved enzymatic activity by its immobilization in a biomembrane model. Journal of Physical Chemistry B. 2011 ; 115( 16): 4801-4809.[citado 2025 out. 08 ]
    • Vancouver

      Monteiro DS, Nobre TM, Zaniquelli MED. Hyaluronidase behavior at the air/liquid and air/lipid interfaces and improved enzymatic activity by its immobilization in a biomembrane model. Journal of Physical Chemistry B. 2011 ; 115( 16): 4801-4809.[citado 2025 out. 08 ]
  • Source: Planta Médica. Unidade: FCFRP

    Subjects: LEISHMANIA, SESQUITERPENOS, QUÍMICA, ESPECTROSCOPIA

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      MACHADO, Fernanda Lacerda da Silva et al. Antileishmanial sesquiterpenes from the Brazilian red alga lourencia dendroidea [Carta]. Planta Médica. Stuttgart: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 08 out. 2025. , 2011
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      Machado, F. L. da S., Lima, W. P., Rossi Bergmann, B., Gestinari, L. M. de S., Fujii, M. T., Paula, J. C. de, et al. (2011). Antileishmanial sesquiterpenes from the Brazilian red alga lourencia dendroidea [Carta]. Planta Médica. Stuttgart: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Machado FL da S, Lima WP, Rossi Bergmann B, Gestinari LM de S, Fujii MT, Paula JC de, Costa SS, Lopes NP, Kaiser CR, Soares AR. Antileishmanial sesquiterpenes from the Brazilian red alga lourencia dendroidea [Carta]. Planta Médica. 2011 ; 77( 7): 733-735.[citado 2025 out. 08 ]
    • Vancouver

      Machado FL da S, Lima WP, Rossi Bergmann B, Gestinari LM de S, Fujii MT, Paula JC de, Costa SS, Lopes NP, Kaiser CR, Soares AR. Antileishmanial sesquiterpenes from the Brazilian red alga lourencia dendroidea [Carta]. Planta Médica. 2011 ; 77( 7): 733-735.[citado 2025 out. 08 ]
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      SASS, Daiane Cristina et al. Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, v. 52, n. 41, p. 5371-5374, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.08.039. Acesso em: 08 out. 2025.
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      Sass, D. C., Lucca Júnior, E. C. de, Barbosa, J. da S., Oliveira, K. T. de, & Constantino, M. G. (2011). Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, 52( 41), 5371-5374. doi:10.1016/j.tetlet.2011.08.039
    • NLM

      Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
    • Vancouver

      Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      NAZARIO, Carlos E. D. et al. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, v. 52, n. 32, p. 4177-4181, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.06.004. Acesso em: 08 out. 2025.
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      Nazario, C. E. D., Santana, A. S., Kawasoko, C. Y., Carollo, C. A., Hurtado, G. R., Viana, L. H., et al. (2011). Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, 52( 32), 4177-4181. doi:10.1016/j.tetlet.2011.06.004
    • NLM

      Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
    • Vancouver

      Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
  • Source: Journal of Applied Polymer Science. Unidade: FFCLRP

    Subjects: TERMOGRAVIMETRIA, QUÍMICA, ESPECTROSCOPIA INFRAVERMELHA

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      MARQUES, Rosalva S. et al. Synthesis and characterization of semi-interpenetrating networks based on poly(dimethylsiloxane) and poly(vinyl alcohol). Journal of Applied Polymer Science, v. 115, n. 1, p. 158-166, 2010Tradução . . Disponível em: https://doi.org/10.1002/app.31006. Acesso em: 08 out. 2025.
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      Marques, R. S., Mac Leod, T. C. O., Yoshida, I. V. P., Mano, V., Assis, M. das D., & Schiavon, M. A. (2010). Synthesis and characterization of semi-interpenetrating networks based on poly(dimethylsiloxane) and poly(vinyl alcohol). Journal of Applied Polymer Science, 115( 1), 158-166. doi:10.1002/app.31006
    • NLM

      Marques RS, Mac Leod TCO, Yoshida IVP, Mano V, Assis M das D, Schiavon MA. Synthesis and characterization of semi-interpenetrating networks based on poly(dimethylsiloxane) and poly(vinyl alcohol) [Internet]. Journal of Applied Polymer Science. 2010 ; 115( 1): 158-166.[citado 2025 out. 08 ] Available from: https://doi.org/10.1002/app.31006
    • Vancouver

      Marques RS, Mac Leod TCO, Yoshida IVP, Mano V, Assis M das D, Schiavon MA. Synthesis and characterization of semi-interpenetrating networks based on poly(dimethylsiloxane) and poly(vinyl alcohol) [Internet]. Journal of Applied Polymer Science. 2010 ; 115( 1): 158-166.[citado 2025 out. 08 ] Available from: https://doi.org/10.1002/app.31006
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Subjects: FARMÁCIA, BIOQUÍMICA, QUÍMICA

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      DABDOUB, Miguel Joaquim et al. Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene. Tetrahedron Letters, v. 51, n. 13, p. 1666-1670, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.01.066. Acesso em: 08 out. 2025.
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      Dabdoub, M. J., Dabdoub, V. B., Baroni, A. C. de M., Hurtado, G. R., & Barbosa, S. L. (2010). Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene. Tetrahedron Letters, 51( 13), 1666-1670. doi:10.1016/j.tetlet.2010.01.066
    • NLM

      Dabdoub MJ, Dabdoub VB, Baroni AC de M, Hurtado GR, Barbosa SL. Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene [Internet]. Tetrahedron Letters. 2010 ; 51( 13): 1666-1670.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2010.01.066
    • Vancouver

      Dabdoub MJ, Dabdoub VB, Baroni AC de M, Hurtado GR, Barbosa SL. Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene [Internet]. Tetrahedron Letters. 2010 ; 51( 13): 1666-1670.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2010.01.066
  • Source: Inorganic Chemistry. Unidade: FFCLRP

    Assunto: QUÍMICA

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      CAMARGO, Maryene A. et al. Efficient phosphodiester hydrolysis by luminescent terbium (III) and Europium (III) complexes. Inorganic Chemistry, v. 46, n. 13, p. 6013-6025, 2010Tradução . . Acesso em: 08 out. 2025.
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      Camargo, M. A., Neves, A., Bortoluzzi, A. J., Szpoganicz, B., Fisher, F. L., Terenzi, H., et al. (2010). Efficient phosphodiester hydrolysis by luminescent terbium (III) and Europium (III) complexes. Inorganic Chemistry, 46( 13), 6013-6025.
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      Camargo MA, Neves A, Bortoluzzi AJ, Szpoganicz B, Fisher FL, Terenzi H, Serra OA, Santos VG, Vaz BG, Eberlin MN. Efficient phosphodiester hydrolysis by luminescent terbium (III) and Europium (III) complexes. Inorganic Chemistry. 2010 ; 46( 13): 6013-6025.[citado 2025 out. 08 ]
    • Vancouver

      Camargo MA, Neves A, Bortoluzzi AJ, Szpoganicz B, Fisher FL, Terenzi H, Serra OA, Santos VG, Vaz BG, Eberlin MN. Efficient phosphodiester hydrolysis by luminescent terbium (III) and Europium (III) complexes. Inorganic Chemistry. 2010 ; 46( 13): 6013-6025.[citado 2025 out. 08 ]
  • Source: Bioorganic and Medicinal Chemistry. Unidades: FCFRP, FMRP

    Subjects: TRYPANOSOMA CRUZI, QUÍMICA

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      CARVALHO, Ivone et al. 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase. Bioorganic and Medicinal Chemistry, v. 18, n. 7, p. 2412-2427, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2010.02.053. Acesso em: 08 out. 2025.
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      Carvalho, I., Andrade, P., Campo, V. L., Guedes, P. M. M., Sesti-Costa, R., Silva, J. S. da, et al. (2010). 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase. Bioorganic and Medicinal Chemistry, 18( 7), 2412-2427. doi:10.1016/j.bmc.2010.02.053
    • NLM

      Carvalho I, Andrade P, Campo VL, Guedes PMM, Sesti-Costa R, Silva JS da, Schenkman S, Dedola S, Hill L, Rejzek M, Nepogodiev SA, Field RA. 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 7): 2412-2427.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.bmc.2010.02.053
    • Vancouver

      Carvalho I, Andrade P, Campo VL, Guedes PMM, Sesti-Costa R, Silva JS da, Schenkman S, Dedola S, Hill L, Rejzek M, Nepogodiev SA, Field RA. 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 7): 2412-2427.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.bmc.2010.02.053
  • Source: Synlett. Unidade: FFCLRP

    Assunto: QUÍMICA

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      DABDOUB, Miguel Joaquim et al. Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes. Synlett, n. 6, p. 986-990, 2009Tradução . . Disponível em: https://doi.org/10.1055/s-0028-1088196. Acesso em: 08 out. 2025.
    • APA

      Dabdoub, M. J., Dabdoub, V. B., Lenardão, É. J., Hurtado, G. R., Barbosa, S. L., Guerrero Júnior, P. G., et al. (2009). Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes. Synlett, ( 6), 986-990. doi:10.1055/s-0028-1088196
    • NLM

      Dabdoub MJ, Dabdoub VB, Lenardão ÉJ, Hurtado GR, Barbosa SL, Guerrero Júnior PG, Nazario CED, Viana LH, Santana AS, Baroni AC de M. Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes [Internet]. Synlett. 2009 ;( 6): 986-990.[citado 2025 out. 08 ] Available from: https://doi.org/10.1055/s-0028-1088196
    • Vancouver

      Dabdoub MJ, Dabdoub VB, Lenardão ÉJ, Hurtado GR, Barbosa SL, Guerrero Júnior PG, Nazario CED, Viana LH, Santana AS, Baroni AC de M. Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes [Internet]. Synlett. 2009 ;( 6): 986-990.[citado 2025 out. 08 ] Available from: https://doi.org/10.1055/s-0028-1088196
  • Source: Journal of Sol-Gel Science and Technology. Unidade: FFCLRP

    Subjects: MANGANÊS, QUÍMICA

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      OLIVEIRA, Luiz Fernando Cappa de et al. Amorphous manganese polyphosphates: preparation, characterization and incorporation of azo dyes. Journal of Sol-Gel Science and Technology, v. 50, n. 2, p. 158-163, 2009Tradução . . Disponível em: https://doi.org/10.1007/s10971-009-1965-7. Acesso em: 08 out. 2025.
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      Oliveira, L. F. C. de, Silva, M. A. P., Brandão, A. R., Stephani, R., Oliveira, C. I. R. de, Gonçalves, R. R., et al. (2009). Amorphous manganese polyphosphates: preparation, characterization and incorporation of azo dyes. Journal of Sol-Gel Science and Technology, 50( 2), 158-163. doi:10.1007/s10971-009-1965-7
    • NLM

      Oliveira LFC de, Silva MAP, Brandão AR, Stephani R, Oliveira CIR de, Gonçalves RR, Barbosa AJ, Barud H da S, Messaddeq Y, Ribeiro SJL. Amorphous manganese polyphosphates: preparation, characterization and incorporation of azo dyes [Internet]. Journal of Sol-Gel Science and Technology. 2009 ; 50( 2): 158-163.[citado 2025 out. 08 ] Available from: https://doi.org/10.1007/s10971-009-1965-7
    • Vancouver

      Oliveira LFC de, Silva MAP, Brandão AR, Stephani R, Oliveira CIR de, Gonçalves RR, Barbosa AJ, Barud H da S, Messaddeq Y, Ribeiro SJL. Amorphous manganese polyphosphates: preparation, characterization and incorporation of azo dyes [Internet]. Journal of Sol-Gel Science and Technology. 2009 ; 50( 2): 158-163.[citado 2025 out. 08 ] Available from: https://doi.org/10.1007/s10971-009-1965-7
  • Source: Synlett. Unidade: IQSC

    Subjects: PRODUTOS NATURAIS, QUÍMICA

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      BURTOLOSO, Antonio Carlos Bender. Catalytic enantioselective 'beta'-arylation of carbonyl compounds. Synlett, n. 2, p. 320-327, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf. Acesso em: 08 out. 2025.
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      Burtoloso, A. C. B. (2009). Catalytic enantioselective 'beta'-arylation of carbonyl compounds. Synlett, ( 2), 320-327. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
    • NLM

      Burtoloso ACB. Catalytic enantioselective 'beta'-arylation of carbonyl compounds [Internet]. Synlett. 2009 ;( 2): 320-327.[citado 2025 out. 08 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
    • Vancouver

      Burtoloso ACB. Catalytic enantioselective 'beta'-arylation of carbonyl compounds [Internet]. Synlett. 2009 ;( 2): 320-327.[citado 2025 out. 08 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
  • Source: Journal of Molecular Structure : Theochem. Unidade: IQSC

    Subjects: QUÍMICA, RAIOS X, FLAVONÓIDES

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    • ABNT

      LAMEIRA, J. et al. A combined x-ray and theoretical study of flavonoid compounds with anti-inflammatory activity. Journal of Molecular Structure : Theochem, v. 862, n. 1-3, p. 16-20, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.theochem.2008.04.029. Acesso em: 08 out. 2025.
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      Lameira, J., Alves, C. N., Santos, L. S., Santos, A. S., Santos, R. H. de A., Souza Jr., J., et al. (2008). A combined x-ray and theoretical study of flavonoid compounds with anti-inflammatory activity. Journal of Molecular Structure : Theochem, 862( 1-3), 16-20. doi:10.1016/j.theochem.2008.04.029
    • NLM

      Lameira J, Alves CN, Santos LS, Santos AS, Santos RH de A, Souza Jr. J, Silva CC, Silva ABF da. A combined x-ray and theoretical study of flavonoid compounds with anti-inflammatory activity [Internet]. Journal of Molecular Structure : Theochem. 2008 ; 862( 1-3): 16-20.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.theochem.2008.04.029
    • Vancouver

      Lameira J, Alves CN, Santos LS, Santos AS, Santos RH de A, Souza Jr. J, Silva CC, Silva ABF da. A combined x-ray and theoretical study of flavonoid compounds with anti-inflammatory activity [Internet]. Journal of Molecular Structure : Theochem. 2008 ; 862( 1-3): 16-20.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.theochem.2008.04.029
  • Source: Tetrahedron. Unidade: IQSC

    Subjects: PRODUTOS NATURAIS, QUÍMICA, PRODUTOS NATURAIS

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    • ABNT

      BURTOLOSO, Antonio Carlos Bender e CORREIA, Carlos Roque Duarte. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones. Tetrahedron, v. 64, n. 42, p. 9928-9936, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.08.001. Acesso em: 08 out. 2025.
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      Burtoloso, A. C. B., & Correia, C. R. D. (2008). Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones. Tetrahedron, 64( 42), 9928-9936. doi:10.1016/j.tet.2008.08.001
    • NLM

      Burtoloso ACB, Correia CRD. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones [Internet]. Tetrahedron. 2008 ; 64( 42): 9928-9936.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tet.2008.08.001
    • Vancouver

      Burtoloso ACB, Correia CRD. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones [Internet]. Tetrahedron. 2008 ; 64( 42): 9928-9936.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.tet.2008.08.001

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