Filtros : "IQ008" "Reino Unido" Removidos: "Universidade Estadual de Campinas (UNICAMP)" "Zílio, Sérgio Carlos" "Holandês" "Simpósio em Ciência e Engenharia de Materiais - SICEM" Limpar

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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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] 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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109
  • 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: 07 jul. 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
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      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 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
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      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 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
  • 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: 07 jul. 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 jul. 07 ] Available from: https://doi.org/10.1039/c5pp00152h
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      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 jul. 07 ] 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: 07 jul. 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 jul. 07 ]
    • 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 jul. 07 ]
  • Source: Dalton Transactions. Unidade: IQ

    Assunto: MATERIAIS NANOESTRUTURADOS

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      WANG, Pei-Xi et al. Hard-templating of Prussian blue analogues in mesoporous silica and organosilica. Dalton Transactions, v. 44, n. 33, p. 14724-14731, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5dt02213d. Acesso em: 07 jul. 2024.
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      Wang, P. -X., Zamarion, V. de M., Hamad, W. Y., & MacLachlan, M. J. (2015). Hard-templating of Prussian blue analogues in mesoporous silica and organosilica. Dalton Transactions, 44( 33), 14724-14731. doi:10.1039/c5dt02213d
    • NLM

      Wang P-X, Zamarion V de M, Hamad WY, MacLachlan MJ. Hard-templating of Prussian blue analogues in mesoporous silica and organosilica [Internet]. Dalton Transactions. 2015 ; 44( 33): 14724-14731.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5dt02213d
    • Vancouver

      Wang P-X, Zamarion V de M, Hamad WY, MacLachlan MJ. Hard-templating of Prussian blue analogues in mesoporous silica and organosilica [Internet]. Dalton Transactions. 2015 ; 44( 33): 14724-14731.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5dt02213d
  • Source: Food Chemistry. Unidade: IQ

    Subjects: CROMATOGRAFIA LÍQUIDA, MORANGO, ANTIOXIDANTES

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      CANUTO, Gisele André Baptista et al. Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power. Food Chemistry, v. 192, p. 566-574, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.foodchem.2015.06.095. Acesso em: 07 jul. 2024.
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      Canuto, G. A. B., Oliveira, D. R., Conceição, L. S. M. da, Farah, J. P. S., & Tavares, M. F. M. (2015). Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power. Food Chemistry, 192, 566-574. doi:10.1016/j.foodchem.2015.06.095
    • NLM

      Canuto GAB, Oliveira DR, Conceição LSM da, Farah JPS, Tavares MFM. Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power [Internet]. Food Chemistry. 2015 ; 192 566-574.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.foodchem.2015.06.095
    • Vancouver

      Canuto GAB, Oliveira DR, Conceição LSM da, Farah JPS, Tavares MFM. Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power [Internet]. Food Chemistry. 2015 ; 192 566-574.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.foodchem.2015.06.095
  • Source: RSC Advances. Unidade: IQ

    Subjects: LIPASE, SÍNTESE ORGÂNICA

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      MARTINS, Rodrigo S et al. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols. RSC Advances, v. 5, n. 70, p. 56599-56605, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ra06469d. Acesso em: 07 jul. 2024.
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      Martins, R. S., Ahmad, A., Silva Junior, L. F. da, & Andrade, L. H. (2015). Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols. RSC Advances, 5( 70), 56599-56605. doi:10.1039/c5ra06469d
    • NLM

      Martins RS, Ahmad A, Silva Junior LF da, Andrade LH. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols [Internet]. RSC Advances. 2015 ; 5( 70): 56599-56605.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra06469d
    • Vancouver

      Martins RS, Ahmad A, Silva Junior LF da, Andrade LH. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols [Internet]. RSC Advances. 2015 ; 5( 70): 56599-56605.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra06469d
  • Source: Polymer Chemistry. Unidade: IQ

    Assunto: POLÍMEROS (QUÍMICA ORGÂNICA)

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      HAVEN, Joris J et al. Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations. Polymer Chemistry, v. 6, n. 31, p. 5752-5765 : + Supplementary materials ( S1-S15), 2015Tradução . . Disponível em: https://doi.org/10.1039/c5py00485c. Acesso em: 07 jul. 2024.
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      Haven, J. J., Vandenbergh, J., Kurita, R., Gruber, J., & Junkers, T. (2015). Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations. Polymer Chemistry, 6( 31), 5752-5765 : + Supplementary materials ( S1-S15). doi:10.1039/c5py00485c
    • NLM

      Haven JJ, Vandenbergh J, Kurita R, Gruber J, Junkers T. Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations [Internet]. Polymer Chemistry. 2015 ; 6( 31): 5752-5765 : + Supplementary materials ( S1-S15).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5py00485c
    • Vancouver

      Haven JJ, Vandenbergh J, Kurita R, Gruber J, Junkers T. Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations [Internet]. Polymer Chemistry. 2015 ; 6( 31): 5752-5765 : + Supplementary materials ( S1-S15).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5py00485c
  • Source: RSC Advances. Unidade: IQ

    Subjects: ELETROQUÍMICA, VOLTAMETRIA

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      DOMÉNECH-CARBÓ, Antonio et al. Electrochemical ecology: VIMP monitoring of plant defense against external stressors. RSC Advances, v. 5, p. 61006-61011, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ra11336a. Acesso em: 07 jul. 2024.
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      Doménech-Carbó, A., Cebrian Torreyon, G., Souto, A. L., Moraes, M. M. de, Kato, M. J., Tavares, J. F., & Barbosa Filho, J. M. (2015). Electrochemical ecology: VIMP monitoring of plant defense against external stressors. RSC Advances, 5, 61006-61011. doi:10.1039/c5ra11336a
    • NLM

      Doménech-Carbó A, Cebrian Torreyon G, Souto AL, Moraes MM de, Kato MJ, Tavares JF, Barbosa Filho JM. Electrochemical ecology: VIMP monitoring of plant defense against external stressors [Internet]. RSC Advances. 2015 ; 5 61006-61011.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra11336a
    • Vancouver

      Doménech-Carbó A, Cebrian Torreyon G, Souto AL, Moraes MM de, Kato MJ, Tavares JF, Barbosa Filho JM. Electrochemical ecology: VIMP monitoring of plant defense against external stressors [Internet]. RSC Advances. 2015 ; 5 61006-61011.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra11336a
  • Source: Chemical Communications. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA

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      UTAKA, Aline e CAVALCANTI, Livia N e SILVA JUNIOR, Luiz Fernando da. Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, v. 50, n. 29, p. 3810-3813, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4cc00608a. Acesso em: 07 jul. 2024.
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      Utaka, A., Cavalcanti, L. N., & Silva Junior, L. F. da. (2014). Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, 50( 29), 3810-3813. doi:10.1039/c4cc00608a
    • NLM

      Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4cc00608a
    • Vancouver

      Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4cc00608a
  • Source: New Journal of Chemistry. Unidade: IQ

    Subjects: BORO, LISOSSOMOS

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      MILANI, Priscila et al. Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors†. New Journal of Chemistry, p. 3-15 : + Supplementary materials ( S1-S13), 2014Tradução . . Disponível em: https://doi.org/10.1039/c4nj00612g. Acesso em: 07 jul. 2024.
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      Milani, P., Demasi, M., Rezende, L. de, Amaral, A. T. do, & Andrade, L. H. (2014). Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors†. New Journal of Chemistry, 3-15 : + Supplementary materials ( S1-S13). doi:10.1039/c4nj00612g
    • NLM

      Milani P, Demasi M, Rezende L de, Amaral AT do, Andrade LH. Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors† [Internet]. New Journal of Chemistry. 2014 ; 3-15 : + Supplementary materials ( S1-S13).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00612g
    • Vancouver

      Milani P, Demasi M, Rezende L de, Amaral AT do, Andrade LH. Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors† [Internet]. New Journal of Chemistry. 2014 ; 3-15 : + Supplementary materials ( S1-S13).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00612g
  • Source: Tetrahedron. Unidade: IQ

    Assunto: BIOGRAFIAS

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      SANTOS, Alcindo Aparecido dos. Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.tet.2014.03.077. Acesso em: 07 jul. 2024. , 2014
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      Santos, A. A. dos. (2014). Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. 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.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2014.03.077
    • Vancouver

      Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2014.03.077
  • Source: Biophysical Journal. Conference titles: Annual Meeting of the Biophysics Society. Unidade: IQ

    Subjects: LIPÍDEOS, SAIS

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      FUNARI, Sérgio S e DI VITTA, Cláudio e MARZORATI, Liliana. Pyridinium salts influence on lipid bilayers. Biophysical Journal. Cambridge: Instituto de Química, Universidade de São Paulo. . Acesso em: 07 jul. 2024. , 2014
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      Funari, S. S., Di Vitta, C., & Marzorati, L. (2014). Pyridinium salts influence on lipid bilayers. Biophysical Journal. Cambridge: Instituto de Química, Universidade de São Paulo.
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      Funari SS, Di Vitta C, Marzorati L. Pyridinium salts influence on lipid bilayers. Biophysical Journal. 2014 ; 106( 2): 90a res. 482.[citado 2024 jul. 07 ]
    • Vancouver

      Funari SS, Di Vitta C, Marzorati L. Pyridinium salts influence on lipid bilayers. Biophysical Journal. 2014 ; 106( 2): 90a res. 482.[citado 2024 jul. 07 ]
  • Source: Journal of Peptide Science. Unidades: IQ, ICB

    Subjects: ANGIOTENSINA II, MALÁRIA, PLASMODIUM

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      SILVA, Adriana Farias da et al. Antiplasmodial activity study of angiotensin II via ALA scan analogs. Journal of Peptide Science, v. 20, n. 8, p. 640-648, 2014Tradução . . Disponível em: https://doi.org/10.1002/psc.2641. Acesso em: 07 jul. 2024.
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      Silva, A. F. da, Bastos, E. L., Torres, M. D. T., Silva, A. L. C. da, Ioshino, R. S., Capurro, M. de L., et al. (2014). Antiplasmodial activity study of angiotensin II via ALA scan analogs. Journal of Peptide Science, 20( 8), 640-648. doi:10.1002/psc.2641
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      Silva AF da, Bastos EL, Torres MDT, Silva ALC da, Ioshino RS, Capurro M de L, Alves FL, Miranda A, Vieira R de FF, Oliveira Junior VX. Antiplasmodial activity study of angiotensin II via ALA scan analogs [Internet]. Journal of Peptide Science. 2014 ; 20( 8): 640-648.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1002/psc.2641
    • Vancouver

      Silva AF da, Bastos EL, Torres MDT, Silva ALC da, Ioshino RS, Capurro M de L, Alves FL, Miranda A, Vieira R de FF, Oliveira Junior VX. Antiplasmodial activity study of angiotensin II via ALA scan analogs [Internet]. Journal of Peptide Science. 2014 ; 20( 8): 640-648.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1002/psc.2641
  • Source: Journal of Materials Chemistry C. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, ELETROQUÍMICA, POLÍMEROS (QUÍMICA ORGÂNICA)

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      CARVALHO, Tânia et al. Ion jelly: a novel sensing material for gas sensors and electronic noses. Journal of Materials Chemistry C, v. 2, n. 4, p. 696-700, 2014Tradução . . Disponível em: https://doi.org/10.1039/c3tc31496k. Acesso em: 07 jul. 2024.
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      Carvalho, T., Vidinha, P., Vieira, B. R., Li, R. W. C., & Gruber, J. (2014). Ion jelly: a novel sensing material for gas sensors and electronic noses. Journal of Materials Chemistry C, 2( 4), 696-700. doi:10.1039/c3tc31496k
    • NLM

      Carvalho T, Vidinha P, Vieira BR, Li RWC, Gruber J. Ion jelly: a novel sensing material for gas sensors and electronic noses [Internet]. Journal of Materials Chemistry C. 2014 ; 2( 4): 696-700.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c3tc31496k
    • Vancouver

      Carvalho T, Vidinha P, Vieira BR, Li RWC, Gruber J. Ion jelly: a novel sensing material for gas sensors and electronic noses [Internet]. Journal of Materials Chemistry C. 2014 ; 2( 4): 696-700.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c3tc31496k
  • Source: New Journal of Chemistry. Unidades: FFCLRP, IQ

    Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS

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      REDDY, Kishore Kumar Reddy Kachi et al. Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry. New Journal of Chemistry, v. 38, n. 6, p. 2262-2264 : + Supplementary materials ( S1-S35), 2014Tradução . . Disponível em: https://doi.org/10.1039/c4nj00284a. Acesso em: 07 jul. 2024.
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      Reddy, K. K. R. K., Cavallini, T. de S., Demets, G. J. -F., & Silva Junior, L. F. da. (2014). Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry. New Journal of Chemistry, 38( 6), 2262-2264 : + Supplementary materials ( S1-S35). doi:10.1039/c4nj00284a
    • NLM

      Reddy KKRK, Cavallini T de S, Demets GJ-F, Silva Junior LF da. Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry [Internet]. New Journal of Chemistry. 2014 ; 38( 6): 2262-2264 : + Supplementary materials ( S1-S35).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00284a
    • Vancouver

      Reddy KKRK, Cavallini T de S, Demets GJ-F, Silva Junior LF da. Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry [Internet]. New Journal of Chemistry. 2014 ; 38( 6): 2262-2264 : + Supplementary materials ( S1-S35).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00284a
  • Source: Phytochemistry. Unidade: IQ

    Subjects: ONTOGENIA, FITOQUÍMICA

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      GAIA, Anderson Melo et al. Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth. Phytochemistry, v. 106, p. 86-93, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2014.06.013. Acesso em: 07 jul. 2024.
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      Gaia, A. M., Yamaguchi, L. F., Jeffrey, C. S., & Kato, M. J. (2014). Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth. Phytochemistry, 106, 86-93. doi:10.1016/j.phytochem.2014.06.013
    • NLM

      Gaia AM, Yamaguchi LF, Jeffrey CS, Kato MJ. Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth [Internet]. Phytochemistry. 2014 ; 106 86-93.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2014.06.013
    • Vancouver

      Gaia AM, Yamaguchi LF, Jeffrey CS, Kato MJ. Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth [Internet]. Phytochemistry. 2014 ; 106 86-93.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2014.06.013
  • Source: Dyes and Pigments. Unidade: IQ

    Subjects: FLUORESCÊNCIA, MERCÚRIO (ELEMENTO QUÍMICO)

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      NÚÑEZ, Cristina et al. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices. Dyes and Pigments, v. 101, p. 156-163, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.09.019. Acesso em: 07 jul. 2024.
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      Núñez, C., Diniz, M., Santos, A. A. dos, Capelo, J. L., & Lodeiro, C. (2014). New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices. Dyes and Pigments, 101, 156-163. doi:10.1016/j.dyepig.2013.09.019
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      Núñez C, Diniz M, Santos AA dos, Capelo JL, Lodeiro C. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices [Internet]. Dyes and Pigments. 2014 ; 101 156-163.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.09.019
    • Vancouver

      Núñez C, Diniz M, Santos AA dos, Capelo JL, Lodeiro C. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices [Internet]. Dyes and Pigments. 2014 ; 101 156-163.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.09.019
  • Source: Journal of Sulfur Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      MARZORATI, Liliana et al. On the thermal pummerer rearrangement of substituted sulfoxides. Journal of Sulfur Chemistry, v. 35, n. 3, p. 248-260, 2014Tradução . . Disponível em: https://doi.org/10.1080/17415993.2013.853066. Acesso em: 07 jul. 2024.
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      Marzorati, L., Yoshikawa, E. K. C., Braga, A. A. C., & Di Vitta, C. (2014). On the thermal pummerer rearrangement of substituted sulfoxides. Journal of Sulfur Chemistry, 35( 3), 248-260. doi:10.1080/17415993.2013.853066
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      Marzorati L, Yoshikawa EKC, Braga AAC, Di Vitta C. On the thermal pummerer rearrangement of substituted sulfoxides [Internet]. Journal of Sulfur Chemistry. 2014 ; 35( 3): 248-260.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1080/17415993.2013.853066
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      Marzorati L, Yoshikawa EKC, Braga AAC, Di Vitta C. On the thermal pummerer rearrangement of substituted sulfoxides [Internet]. Journal of Sulfur Chemistry. 2014 ; 35( 3): 248-260.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1080/17415993.2013.853066

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