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  • Source: ChemistrySelect. Unidades: FCFRP, IQSC

    Assunto: QUÍMICA VERDE

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      LIMA, Rafaely Nascimento; VAZ, Artur de Lara Lima; CLOSOSKI, Giuliano Cesar; PORTO, André Luiz Meleiro. Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate. ChemistrySelect, Weinheim, v. 6, p. 21, 2021. Disponível em: < https://doi.org/10.1002/slct.202100883 > DOI: 10.1002/slct.202100883.
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      Lima, R. N., Vaz, A. de L. L., Clososki, G. C., & Porto, A. L. M. (2021). Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate. ChemistrySelect, 6, 21. doi:10.1002/slct.202100883
    • NLM

      Lima RN, Vaz A de LL, Clososki GC, Porto ALM. Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate [Internet]. ChemistrySelect. 2021 ;6 21.Available from: https://doi.org/10.1002/slct.202100883
    • Vancouver

      Lima RN, Vaz A de LL, Clososki GC, Porto ALM. Sustainable Synthesis of Amides from Ethyl 3‐(4‐Hydroxyphenyl) Propionate [Internet]. ChemistrySelect. 2021 ;6 21.Available from: https://doi.org/10.1002/slct.202100883
  • Source: ChemistrySelect. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, CATALISADORES

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      ZANIN, Lucas Lima; PORTO, André Luiz Meleiro. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, Weinheim, v. 5, n. 28, p. 8604-8608, 2020. Disponível em: < https://doi.org/10.1002/slct.202001830 > DOI: 10.1002/slct.202001830.
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      Zanin, L. L., & Porto, A. L. M. (2020). HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, 5( 28), 8604-8608. doi:10.1002/slct.202001830
    • NLM

      Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.Available from: https://doi.org/10.1002/slct.202001830
    • Vancouver

      Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.Available from: https://doi.org/10.1002/slct.202001830
  • Source: ChemistrySelect. Unidade: IQSC

    Subjects: ULTRASSOM, RAIOS X

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      KHALID, Muhammad; ALI, Akbar; ABID , Saba; et al. Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry. ChemistrySelect, Weinheim, v. 5, p. , 2020. Disponível em: < https://doi.org/10.1002/slct.202003589 > DOI: 10.1002/slct.202003589.
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      Khalid, M., Ali, A., Abid , S., Tahir, M. N., Khan, M. U., Ashfaq, M., et al. (2020). Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry. ChemistrySelect, 5, . doi:10.1002/slct.202003589
    • NLM

      Khalid M, Ali A, Abid S, Tahir MN, Khan MU, Ashfaq M, Imran M, Ahmad A. Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry [Internet]. ChemistrySelect. 2020 ; 5 .Available from: https://doi.org/10.1002/slct.202003589
    • Vancouver

      Khalid M, Ali A, Abid S, Tahir MN, Khan MU, Ashfaq M, Imran M, Ahmad A. Facile Ultrasound based Synthesis, SCXRD, DFT Exploration of the Substituted AcylHydrazones: An Experimental and Theoretical Slant towards Supramolecular Chemistry [Internet]. ChemistrySelect. 2020 ; 5 .Available from: https://doi.org/10.1002/slct.202003589
  • Source: ChemistrySelect. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      ADERIBIGBE, Abiodun D.; DAY, David P. Syntheses and Applications of Malonamide Derivatives – A Minireview. ChemistrySelect, Weinheim, v. 5, p. 15222–15232, 2020. Disponível em: < https://doi.org/10.1002/slct.202004340 > DOI: 10.1002/slct.202004340.
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      Aderibigbe, A. D., & Day, D. P. (2020). Syntheses and Applications of Malonamide Derivatives – A Minireview. ChemistrySelect, 5, 15222–15232. doi:10.1002/slct.202004340
    • NLM

      Aderibigbe AD, Day DP. Syntheses and Applications of Malonamide Derivatives – A Minireview [Internet]. ChemistrySelect. 2020 ; 5 15222–15232.Available from: https://doi.org/10.1002/slct.202004340
    • Vancouver

      Aderibigbe AD, Day DP. Syntheses and Applications of Malonamide Derivatives – A Minireview [Internet]. ChemistrySelect. 2020 ; 5 15222–15232.Available from: https://doi.org/10.1002/slct.202004340
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: CÉLULAS SOLARES, FILMES FINOS, ELETROQUÍMICA

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      MATOS, Lais Sottili de; AMARAL, Ronaldo Costa; IHA, Neyde Yukie Murakami. New LbL‐TiO2/ZnO compact films to improve performance of dye‐sensitized solar cells. ChemistrySelect, Weinheim, v. 4, n. 1, p. 265-270, 2019. Disponível em: < http://dx.doi.org/10.1002/slct.201802491 > DOI: 10.1002/slct.201802491.
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      Matos, L. S. de, Amaral, R. C., & Iha, N. Y. M. (2019). New LbL‐TiO2/ZnO compact films to improve performance of dye‐sensitized solar cells. ChemistrySelect, 4( 1), 265-270. doi:10.1002/slct.201802491
    • NLM

      Matos LS de, Amaral RC, Iha NYM. New LbL‐TiO2/ZnO compact films to improve performance of dye‐sensitized solar cells [Internet]. ChemistrySelect. 2019 ; 4( 1): 265-270.Available from: http://dx.doi.org/10.1002/slct.201802491
    • Vancouver

      Matos LS de, Amaral RC, Iha NYM. New LbL‐TiO2/ZnO compact films to improve performance of dye‐sensitized solar cells [Internet]. ChemistrySelect. 2019 ; 4( 1): 265-270.Available from: http://dx.doi.org/10.1002/slct.201802491
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: MEDICAMENTO, OSTEOPOROSE

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      ROCHA, Júlio César da; SIHN, Luca Michael; UCHIYAMA, Mayara Klimuk; et al. On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug. ChemistrySelect, Weinheim, v. 4, p. 13926-13931, 2019. Disponível em: < http://dx.doi.org/10.1002/slct.201904149 > DOI: 10.1002/slct.201904149.
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      Rocha, J. C. da, Sihn, L. M., Uchiyama, M. K., Ribeiro, M. A., Franco, M. P., Braga, A. A. C., et al. (2019). On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug. ChemistrySelect, 4, 13926-13931. doi:10.1002/slct.201904149
    • NLM

      Rocha JC da, Sihn LM, Uchiyama MK, Ribeiro MA, Franco MP, Braga AAC, Silveira AT, Toma HE. On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug [Internet]. ChemistrySelect. 2019 ; 4 13926-13931.Available from: http://dx.doi.org/10.1002/slct.201904149
    • Vancouver

      Rocha JC da, Sihn LM, Uchiyama MK, Ribeiro MA, Franco MP, Braga AAC, Silveira AT, Toma HE. On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug [Internet]. ChemistrySelect. 2019 ; 4 13926-13931.Available from: http://dx.doi.org/10.1002/slct.201904149
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: COLESTEROL, LÍQUIDOS IÔNICOS, SURFACTANTES

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      VAID, Zuber S; RAJPUT, Sargam M; KUDDUSHI, Muzammil; et al. Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition. ChemistrySelect, Weinheim, v. 3, n. 4, p. 1300-1308, 2018. Disponível em: < http://dx.doi.org/10.1002/slct.201702561 > DOI: 10.1002/slct.201702561.
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      Vaid, Z. S., Rajput, S. M., Kuddushi, M., Kumar, A., El Seoud, O. A., & Malek, N. I. (2018). Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition. ChemistrySelect, 3( 4), 1300-1308. doi:10.1002/slct.201702561
    • NLM

      Vaid ZS, Rajput SM, Kuddushi M, Kumar A, El Seoud OA, Malek NI. Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition [Internet]. ChemistrySelect. 2018 ; 3( 4): 1300-1308.Available from: http://dx.doi.org/10.1002/slct.201702561
    • Vancouver

      Vaid ZS, Rajput SM, Kuddushi M, Kumar A, El Seoud OA, Malek NI. Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition [Internet]. ChemistrySelect. 2018 ; 3( 4): 1300-1308.Available from: http://dx.doi.org/10.1002/slct.201702561
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: SURFACTANTES, LÍQUIDOS IÔNICOS

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      VAID, Zuber S; RAJPUT, Sargam M; SHAH, Ankit; et al. Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants. ChemistrySelect, Weinheim, v. 3, n. 17, p. 4851-4858, 2018. Disponível em: < http://dx.doi.org/10.1002/slct.201800041 > DOI: 10.1002/slct.201800041.
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      Vaid, Z. S., Rajput, S. M., Shah, A., Kadam, Y., Kumar, A., El Seoud, O. A., et al. (2018). Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants. ChemistrySelect, 3( 17), 4851-4858. doi:10.1002/slct.201800041
    • NLM

      Vaid ZS, Rajput SM, Shah A, Kadam Y, Kumar A, El Seoud OA, Mata JP, Malek NI. Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants [Internet]. ChemistrySelect. 2018 ; 3( 17): 4851-4858.Available from: http://dx.doi.org/10.1002/slct.201800041
    • Vancouver

      Vaid ZS, Rajput SM, Shah A, Kadam Y, Kumar A, El Seoud OA, Mata JP, Malek NI. Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants [Internet]. ChemistrySelect. 2018 ; 3( 17): 4851-4858.Available from: http://dx.doi.org/10.1002/slct.201800041
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: NANOCOMPOSITOS, LUMINESCÊNCIA

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      KHAN, Latif Ullah; ZAMBON, Luis F. M; SANTOS, Jacinete Lima dos; et al. Red-emitting magnetic nanocomposites assembled from Ag-decorated 'Fe IND. 3''O IND. 4'@'SiO IND. 2' and 'Y IND. 2''O IND. 3':'Eu POT. 3+': impact of iron-oxide/silver nanoparticles on 'Eu POT. 3+' emission. ChemistrySelect, Weinheim, v. 3, n. 4, p. 1157-1167, 2018. Disponível em: < http://dx.doi.org/10.1002/slct.201702478 > DOI: 10.1002/slct.201702478.
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      Khan, L. U., Zambon, L. F. M., Santos, J. L. dos, Rodrigues, R. V., Costa, L. S. de, Muraca, D., et al. (2018). Red-emitting magnetic nanocomposites assembled from Ag-decorated 'Fe IND. 3''O IND. 4'@'SiO IND. 2' and 'Y IND. 2''O IND. 3':'Eu POT. 3+': impact of iron-oxide/silver nanoparticles on 'Eu POT. 3+' emission. ChemistrySelect, 3( 4), 1157-1167. doi:10.1002/slct.201702478
    • NLM

      Khan LU, Zambon LFM, Santos JL dos, Rodrigues RV, Costa LS de, Muraca D, Pirota kleber R, Felinto MCF da C, Malta OL, Brito HF de. Red-emitting magnetic nanocomposites assembled from Ag-decorated 'Fe IND. 3''O IND. 4'@'SiO IND. 2' and 'Y IND. 2''O IND. 3':'Eu POT. 3+': impact of iron-oxide/silver nanoparticles on 'Eu POT. 3+' emission [Internet]. ChemistrySelect. 2018 ; 3( 4): 1157-1167.Available from: http://dx.doi.org/10.1002/slct.201702478
    • Vancouver

      Khan LU, Zambon LFM, Santos JL dos, Rodrigues RV, Costa LS de, Muraca D, Pirota kleber R, Felinto MCF da C, Malta OL, Brito HF de. Red-emitting magnetic nanocomposites assembled from Ag-decorated 'Fe IND. 3''O IND. 4'@'SiO IND. 2' and 'Y IND. 2''O IND. 3':'Eu POT. 3+': impact of iron-oxide/silver nanoparticles on 'Eu POT. 3+' emission [Internet]. ChemistrySelect. 2018 ; 3( 4): 1157-1167.Available from: http://dx.doi.org/10.1002/slct.201702478
  • Source: ChemistrySelect. Unidade: IQSC

    Assunto: BIOMASSA

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      METZKER, Gustavo; DIAS, Rafael Mafra de Paula; BURTOLOSO, Antonio Carlos Bender. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities. ChemistrySelect, Weinheim, v. 3, n. 2, p. 368-372, 2018. Disponível em: < https://doi.org/10.1002/slct.201702580 > DOI: 10.1002/slct.201702580.
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      Metzker, G., Dias, R. M. de P., & Burtoloso, A. C. B. (2018). Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities. ChemistrySelect, 3( 2), 368-372. doi:10.1002/slct.201702580
    • NLM

      Metzker G, Dias RM de P, Burtoloso ACB. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities [Internet]. ChemistrySelect. 2018 ; 3( 2): 368-372.Available from: https://doi.org/10.1002/slct.201702580
    • Vancouver

      Metzker G, Dias RM de P, Burtoloso ACB. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities [Internet]. ChemistrySelect. 2018 ; 3( 2): 368-372.Available from: https://doi.org/10.1002/slct.201702580
  • Source: ChemistrySelect. Unidade: FCF

    Subjects: ITÉRBIO, SÓDIO

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      TORNQUIST, Bruna Luisa; BUENO, Gabriel de Paula; WILLIG, Julia Caroline Manzano; et al. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs). ChemistrySelect, Weinheim, v. 3, p. 6358-6363, 2018. Disponível em: < http://dx.doi.org/10.1002/slct.201800673 > DOI: 10.1002/slct.201800673.
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      Tornquist, B. L., Bueno, G. de P., Willig, J. C. M., Oliveira, I. M. de, Stefani, H. A., Rafique, J., et al. (2018). Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs). ChemistrySelect, 3, 6358-6363. doi:10.1002/slct.201800673
    • NLM

      Tornquist BL, Bueno G de P, Willig JCM, Oliveira IM de, Stefani HA, Rafique J, Saba S, Iglesias BA, Botteselle GV, Manarin F. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) [Internet]. ChemistrySelect. 2018 ; 3 6358-6363.Available from: http://dx.doi.org/10.1002/slct.201800673
    • Vancouver

      Tornquist BL, Bueno G de P, Willig JCM, Oliveira IM de, Stefani HA, Rafique J, Saba S, Iglesias BA, Botteselle GV, Manarin F. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) [Internet]. ChemistrySelect. 2018 ; 3 6358-6363.Available from: http://dx.doi.org/10.1002/slct.201800673
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: CÉLULAS SOLARES, ELETROQUÍMICA, DISPERSÃO DA LUZ

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      MUHAMMAD, Niaz; ZANONI, Kassio Papi Silva; IHA, Neyde Yukie Murakami; AHMED, Safeer. The Use of Rutile and Anatase Titania Layers towards Back Light Scattering in Dye-Sensitized Solar Cells. ChemistrySelect, Weinheim, v. 3, p. 10475-10482 : + Supplementary materials (S1-S6), 2018. Disponível em: < http://dx.doi.org/10.1002/slct.201801569 > DOI: 10.1002/slct.201801569.
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      Muhammad, N., Zanoni, K. P. S., Iha, N. Y. M., & Ahmed, S. (2018). The Use of Rutile and Anatase Titania Layers towards Back Light Scattering in Dye-Sensitized Solar Cells. ChemistrySelect, 3, 10475-10482 : + Supplementary materials (S1-S6). doi:10.1002/slct.201801569
    • NLM

      Muhammad N, Zanoni KPS, Iha NYM, Ahmed S. The Use of Rutile and Anatase Titania Layers towards Back Light Scattering in Dye-Sensitized Solar Cells [Internet]. ChemistrySelect. 2018 ; 3 10475-10482 : + Supplementary materials (S1-S6).Available from: http://dx.doi.org/10.1002/slct.201801569
    • Vancouver

      Muhammad N, Zanoni KPS, Iha NYM, Ahmed S. The Use of Rutile and Anatase Titania Layers towards Back Light Scattering in Dye-Sensitized Solar Cells [Internet]. ChemistrySelect. 2018 ; 3 10475-10482 : + Supplementary materials (S1-S6).Available from: http://dx.doi.org/10.1002/slct.201801569
  • Source: ChemistrySelect. Unidade: FCF

    Subjects: PALÁDIO, QUÍMICA FARMACÊUTICA

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      BARBEIRO, Cristiane de Souza; VASCONCELOS, Stanley Nunes Siqueira; OLIVEIRA, Isadora Maria de; et al. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, Weinheim, v. 2, n. 26, p. 8173-8177, 2017. Disponível em: < http://dx.doi.org/10.1002/slct.201701197 > DOI: 10.1002/slct.201701197.
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      Barbeiro, C. de S., Vasconcelos, S. N. S., Oliveira, I. M. de, Zukerman-Schpector, J., Caracelli, I., Maganhi, S. H., & Stefani, H. A. (2017). Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, 2( 26), 8173-8177. doi:10.1002/slct.201701197
    • NLM

      Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.Available from: http://dx.doi.org/10.1002/slct.201701197
    • Vancouver

      Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.Available from: http://dx.doi.org/10.1002/slct.201701197
  • Source: ChemistrySelect. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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      LUCHESE, Angelica M; DI VITTA, Cláudio; MARZORATI, Liliana; YAMAOKA , Patrícia; FUNARI, Sérgio S. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts. ChemistrySelect, Weinheim, v. 2, n. 4, p. 1491-1496, 2017. Disponível em: < http://dx.doi.org/10.1002/slct.201601588 > DOI: 10.1002/slct.201601588.
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      Luchese, A. M., Di Vitta, C., Marzorati, L., Yamaoka , P., & Funari, S. S. (2017). Lipid Matrices destabilization induced by some newly synthesized pyridinium salts. ChemistrySelect, 2( 4), 1491-1496. doi:10.1002/slct.201601588
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      Luchese AM, Di Vitta C, Marzorati L, Yamaoka P, Funari SS. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts [Internet]. ChemistrySelect. 2017 ; 2( 4): 1491-1496.Available from: http://dx.doi.org/10.1002/slct.201601588
    • Vancouver

      Luchese AM, Di Vitta C, Marzorati L, Yamaoka P, Funari SS. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts [Internet]. ChemistrySelect. 2017 ; 2( 4): 1491-1496.Available from: http://dx.doi.org/10.1002/slct.201601588
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: FÍSICO-QUÍMICA, SOLVENTE

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      SILVA, Vitor Hugo Menezes da; SILVA JUNIOR, Luiz Fernando da; BRAGA, Ataualpa Albert Carmo. Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations. ChemistrySelect, Weinheim, v. 1, p. 2706-2711, 2016. Disponível em: < http://dx.doi.org/10.1002/slct.201600228 > DOI: 10.1002/slct.201600228.
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      Silva, V. H. M. da, Silva Junior, L. F. da, & Braga, A. A. C. (2016). Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations. ChemistrySelect, 1, 2706-2711. doi:10.1002/slct.201600228
    • NLM

      Silva VHM da, Silva Junior LF da, Braga AAC. Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations [Internet]. ChemistrySelect. 2016 ; 1 2706-2711.Available from: http://dx.doi.org/10.1002/slct.201600228
    • Vancouver

      Silva VHM da, Silva Junior LF da, Braga AAC. Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations [Internet]. ChemistrySelect. 2016 ; 1 2706-2711.Available from: http://dx.doi.org/10.1002/slct.201600228
  • Source: ChemistrySelect. Unidades: IQ, FCF

    Subjects: MECANISMOS, FLUORESCÊNCIA

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      BARBEIRO, Cristiane S; VASCONCELOS, Stanley Nunes Siqueira; SCHPECTOR, Júlio Zukerman; et al. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, Weinheim, v. 2, p. 5647–5652, 2016. Disponível em: < http://dx.doi.org/10.1002/slct.201601526 > DOI: 10.1002/slct.201601526.
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      Barbeiro, C. S., Vasconcelos, S. N. S., Schpector, J. Z., Caracelli, I., Pimenta, D. C., Rodrigues, A. C. B., et al. (2016). Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, 2, 5647–5652. doi:10.1002/slct.201601526
    • NLM

      Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.Available from: http://dx.doi.org/10.1002/slct.201601526
    • Vancouver

      Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.Available from: http://dx.doi.org/10.1002/slct.201601526
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: BIOLUMINESCÊNCIA, CATÁLISE

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    • ABNT

      SOUZA, Glalci A; PEIXOTO, Mônica M. M; SANTOS, Ana P. F; BAADER, Wilhelm Josef. General acid and base catalysis by phosphate in Peroxyoxalate Chemiluminescence. ChemistrySelect, Weinheim, v. 1, n. 10, p. 2307-2315, 2016. Disponível em: < http://dx.doi.org/10.1002/slct.201600436 > DOI: 10.1002/slct.201600436.
    • APA

      Souza, G. A., Peixoto, M. M. M., Santos, A. P. F., & Baader, W. J. (2016). General acid and base catalysis by phosphate in Peroxyoxalate Chemiluminescence. ChemistrySelect, 1( 10), 2307-2315. doi:10.1002/slct.201600436
    • NLM

      Souza GA, Peixoto MMM, Santos APF, Baader WJ. General acid and base catalysis by phosphate in Peroxyoxalate Chemiluminescence [Internet]. ChemistrySelect. 2016 ; 1( 10): 2307-2315.Available from: http://dx.doi.org/10.1002/slct.201600436
    • Vancouver

      Souza GA, Peixoto MMM, Santos APF, Baader WJ. General acid and base catalysis by phosphate in Peroxyoxalate Chemiluminescence [Internet]. ChemistrySelect. 2016 ; 1( 10): 2307-2315.Available from: http://dx.doi.org/10.1002/slct.201600436

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