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  • Source: Molecules: a journal of synthetic organic and natural product chemistry. Unidade: IQSC

    Subjects: SÍNTESE ORGÂNICA, ELETROQUÍMICA, REDUÇÃO

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      LEI, Yuting et al. One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors. Molecules: a journal of synthetic organic and natural product chemistry, v. 27, p. 7629, 2022Tradução . . Disponível em: https://doi.org/10.3390/molecules27217629. Acesso em: 02 out. 2024.
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      Lei, Y., Madalena, L. dos S., Ossonon, B. D., Bimbi Junior, F. E., Chen, J., Lanza, M. R. de V., & Tavares, A. C. (2022). One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors. Molecules: a journal of synthetic organic and natural product chemistry, 27, 7629. doi:10.3390/molecules27217629
    • NLM

      Lei Y, Madalena L dos S, Ossonon BD, Bimbi Junior FE, Chen J, Lanza MR de V, Tavares AC. One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors [Internet]. Molecules: a journal of synthetic organic and natural product chemistry. 2022 ;27 7629.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules27217629
    • Vancouver

      Lei Y, Madalena L dos S, Ossonon BD, Bimbi Junior FE, Chen J, Lanza MR de V, Tavares AC. One-Step Synthesis of Aminobenzoic Acid Functionalized Graphene Oxide by Electrochemical Exfoliation of Graphite for Oxygen Reduction to Hydrogen Peroxide and Supercapacitors [Internet]. Molecules: a journal of synthetic organic and natural product chemistry. 2022 ;27 7629.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules27217629
  • Source: Chemical Engineering Journal. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, BIODIESEL, IMPRESSÃO, TERCEIRA DIMENSÃO, SIMULAÇÃO

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      SANTANA, Harrson S et al. Design, optimization and scale-up of a new micromixer design based on plate column for organic synthesis. Chemical Engineering Journal, v. 446, p. 1-14 art. 137159, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.cej.2022.137159. Acesso em: 02 out. 2024.
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      Santana, H. S., Haddad, V. A., Calvo, P. V. C., Palma, M. S. A., Silva, A. G. P. da, Noriler, D., et al. (2022). Design, optimization and scale-up of a new micromixer design based on plate column for organic synthesis. Chemical Engineering Journal, 446, 1-14 art. 137159. doi:10.1016/j.cej.2022.137159
    • NLM

      Santana HS, Haddad VA, Calvo PVC, Palma MSA, Silva AGP da, Noriler D, Taranto OP, Silva JL. Design, optimization and scale-up of a new micromixer design based on plate column for organic synthesis [Internet]. Chemical Engineering Journal. 2022 ; 446 1-14 art. 137159.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.cej.2022.137159
    • Vancouver

      Santana HS, Haddad VA, Calvo PVC, Palma MSA, Silva AGP da, Noriler D, Taranto OP, Silva JL. Design, optimization and scale-up of a new micromixer design based on plate column for organic synthesis [Internet]. Chemical Engineering Journal. 2022 ; 446 1-14 art. 137159.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.cej.2022.137159
  • Source: Catalysts. Unidade: FFCLRP

    Subjects: BIOMATERIAIS, IMOBILIZAÇÃO, LIPASE, SÍNTESE ORGÂNICA, CATALISADORES

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      ALNOCH, Robson Carlos et al. Recent trends in biomaterials for immobilization of lipases for application in non-conventional media. Catalysts, v. 10, n. 6, p. 1-29, 2020Tradução . . Disponível em: https://doi.org/10.3390/catal10060697. Acesso em: 02 out. 2024.
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      Alnoch, R. C., Santos, L. A. dos, Almeida, J. M. de, Krieger, N., & Mateo, C. (2020). Recent trends in biomaterials for immobilization of lipases for application in non-conventional media. Catalysts, 10( 6), 1-29. doi:10.3390/catal10060697
    • NLM

      Alnoch RC, Santos LA dos, Almeida JM de, Krieger N, Mateo C. Recent trends in biomaterials for immobilization of lipases for application in non-conventional media [Internet]. Catalysts. 2020 ; 10( 6): 1-29.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/catal10060697
    • Vancouver

      Alnoch RC, Santos LA dos, Almeida JM de, Krieger N, Mateo C. Recent trends in biomaterials for immobilization of lipases for application in non-conventional media [Internet]. Catalysts. 2020 ; 10( 6): 1-29.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/catal10060697
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, SÍNTESE ORGÂNICA

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      SILVA, Vitor Hugo Menezes da et al. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, v. 896, p. 5-15, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2019.05.023. Acesso em: 02 out. 2024.
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      Silva, V. H. M. da, Morgon, N. H., Correia, C. R. D., & Braga, A. A. C. (2019). DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, 896, 5-15. doi:10.1016/j.jorganchem.2019.05.023
    • NLM

      Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023
    • Vancouver

      Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023
  • Source: Frontiers in Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      GALLO, Rafael D. C et al. Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis. Frontiers in Chemistry, v. 7, p. 1-7, 2019Tradução . . Disponível em: https://doi.org/10.3389/fchem.2019.00062. Acesso em: 02 out. 2024.
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      Gallo, R. D. C., Campovilla Junior, O. C., Ahmad, A., & Burtoloso, A. C. B. (2019). Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis. Frontiers in Chemistry, 7, 1-7. doi:10.3389/fchem.2019.00062
    • NLM

      Gallo RDC, Campovilla Junior OC, Ahmad A, Burtoloso ACB. Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis [Internet]. Frontiers in Chemistry. 2019 ; 7 1-7.[citado 2024 out. 02 ] Available from: https://doi.org/10.3389/fchem.2019.00062
    • Vancouver

      Gallo RDC, Campovilla Junior OC, Ahmad A, Burtoloso ACB. Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis [Internet]. Frontiers in Chemistry. 2019 ; 7 1-7.[citado 2024 out. 02 ] Available from: https://doi.org/10.3389/fchem.2019.00062
  • Source: Molecules. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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      SILVA, Siguara Bastos de Lemos e et al. Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine. Molecules, v. 20, n. 1, p. 1475-1494, 2015Tradução . . Disponível em: https://doi.org/10.3390/molecules20011475. Acesso em: 02 out. 2024.
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      Silva, S. B. de L. e, Della Torre, A., Carvalho, J. E. de, Ruiz, A. L. T. G. de, & Silva Junior, L. F. da. (2015). Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine. Molecules, 20( 1), 1475-1494. doi:10.3390/molecules20011475
    • NLM

      Silva SB de L e, Della Torre A, Carvalho JE de, Ruiz ALTG de, Silva Junior LF da. Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine [Internet]. Molecules. 2015 ; 20( 1): 1475-1494.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules20011475
    • Vancouver

      Silva SB de L e, Della Torre A, Carvalho JE de, Ruiz ALTG de, Silva Junior LF da. Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine [Internet]. Molecules. 2015 ; 20( 1): 1475-1494.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules20011475
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: HIDROCARBONOS, SÍNTESE ORGÂNICA

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      BESORA, Maria et al. A computational view on the reactions of hydrocarbons with coinage metal complexes. Journal of Organometallic Chemistry, v. 784, p. 1-12, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2014.10.009. Acesso em: 02 out. 2024.
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      Besora, M., Braga, A. A. C., Sameera, W. M. C., Urbano, J., Fructos, M. R., Pérez, P. J., & Maseras, F. (2015). A computational view on the reactions of hydrocarbons with coinage metal complexes. Journal of Organometallic Chemistry, 784, 1-12. doi:10.1016/j.jorganchem.2014.10.009
    • NLM

      Besora M, Braga AAC, Sameera WMC, Urbano J, Fructos MR, Pérez PJ, Maseras F. A computational view on the reactions of hydrocarbons with coinage metal complexes [Internet]. Journal of Organometallic Chemistry. 2015 ; 784 1-12.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2014.10.009
    • Vancouver

      Besora M, Braga AAC, Sameera WMC, Urbano J, Fructos MR, Pérez PJ, Maseras F. A computational view on the reactions of hydrocarbons with coinage metal complexes [Internet]. Journal of Organometallic Chemistry. 2015 ; 784 1-12.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2014.10.009
  • Source: Molecules. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, SÍNTESE ORGÂNICA

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      SCHPECTOR, Julio Zukermann et al. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, v. 19, n. 2, p. 1990-2003, 2014Tradução . . Disponível em: https://doi.org/10.3390/molecules19021990. Acesso em: 02 out. 2024.
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      Schpector, J. Z., Madureira, L. S., Wulf, G. D., Stefani, H. A., Vasconcelos, S. N. S., Ng, S. W., & Tiekink, E. R. T. (2014). Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, 19( 2), 1990-2003. doi:10.3390/molecules19021990
    • NLM

      Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules19021990
    • Vancouver

      Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules19021990
  • Source: Molecules. Unidade: IQ

    Subjects: ALDEÍDOS, SÍNTESE ORGÂNICA

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      REDDY, Kachi R. Kishore Kumar et al. Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes. Molecules, v. 18, n. 9, p. 11100-11130, 2013Tradução . . Disponível em: https://doi.org/10.3390/molecules180911100. Acesso em: 02 out. 2024.
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      Reddy, K. R. K. K., Rosa, I. M. L. R., Doriguetto, A. C., Bastos, E. L., & Silva Junior, L. F. da. (2013). Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes. Molecules, 18( 9), 11100-11130. doi:10.3390/molecules180911100
    • NLM

      Reddy KRKK, Rosa IMLR, Doriguetto AC, Bastos EL, Silva Junior LF da. Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes [Internet]. Molecules. 2013 ; 18( 9): 11100-11130.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules180911100
    • Vancouver

      Reddy KRKK, Rosa IMLR, Doriguetto AC, Bastos EL, Silva Junior LF da. Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes [Internet]. Molecules. 2013 ; 18( 9): 11100-11130.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules180911100
  • Source: Molecules. Unidade: IQ

    Subjects: LIPASE, SÍNTESE ORGÂNICA

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      PALMEIRA, Dayvson J e ABREU, Juliana C e ANDRADE, Leandro Helgueira. Lipase-catalyzed kinetic resolution of aryltrimethylsilyl chiral alcohols. Molecules, v. 16, n. 11, p. 9697-9713, 2011Tradução . . Disponível em: https://doi.org/10.3390/molecules16119697. Acesso em: 02 out. 2024.
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      Palmeira, D. J., Abreu, J. C., & Andrade, L. H. (2011). Lipase-catalyzed kinetic resolution of aryltrimethylsilyl chiral alcohols. Molecules, 16( 11), 9697-9713. doi:10.3390/molecules16119697
    • NLM

      Palmeira DJ, Abreu JC, Andrade LH. Lipase-catalyzed kinetic resolution of aryltrimethylsilyl chiral alcohols [Internet]. Molecules. 2011 ; 16( 11): 9697-9713.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules16119697
    • Vancouver

      Palmeira DJ, Abreu JC, Andrade LH. Lipase-catalyzed kinetic resolution of aryltrimethylsilyl chiral alcohols [Internet]. Molecules. 2011 ; 16( 11): 9697-9713.[citado 2024 out. 02 ] Available from: https://doi.org/10.3390/molecules16119697
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, SÍNTESE ORGÂNICA

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      VARGAS, Fabrício e COMASSETO, João Valdir. Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines. Journal of Organometallic Chemistry, v. 694, n. 1, p. 122-126, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.09.025. Acesso em: 02 out. 2024.
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      Vargas, F., & Comasseto, J. V. (2009). Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines. Journal of Organometallic Chemistry, 694( 1), 122-126. doi:10.1016/j.jorganchem.2008.09.025
    • NLM

      Vargas F, Comasseto JV. Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines [Internet]. Journal of Organometallic Chemistry. 2009 ; 694( 1): 122-126.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.09.025
    • Vancouver

      Vargas F, Comasseto JV. Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines [Internet]. Journal of Organometallic Chemistry. 2009 ; 694( 1): 122-126.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.09.025
  • Source: Journal of Organometallic Chemistry. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, BORO

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      BELLOMO, Ana e GONZALES, David e STEFANI, Hélio Alexandre. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach. Journal of Organometallic Chemistry, v. 693, n. 6, p. 1136-1142, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.01.006. Acesso em: 02 out. 2024.
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      Bellomo, A., Gonzales, D., & Stefani, H. A. (2008). Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach. Journal of Organometallic Chemistry, 693( 6), 1136-1142. doi:10.1016/j.jorganchem.2008.01.006
    • NLM

      Bellomo A, Gonzales D, Stefani HA. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach [Internet]. Journal of Organometallic Chemistry. 2008 ;693( 6): 1136-1142.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.01.006
    • Vancouver

      Bellomo A, Gonzales D, Stefani HA. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach [Internet]. Journal of Organometallic Chemistry. 2008 ;693( 6): 1136-1142.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.01.006
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      COMASSETO, João Valdir et al. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides. Journal of Organometallic Chemistry, v. 693, n. 17, p. 2929-2936, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.06.014. Acesso em: 02 out. 2024.
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      Comasseto, J. V., Gariani, R. A., Princival, J. L., Dos Santos, A. A., & Zinn, F. K. (2008). Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides. Journal of Organometallic Chemistry, 693( 17), 2929-2936. doi:10.1016/j.jorganchem.2008.06.014
    • NLM

      Comasseto JV, Gariani RA, Princival JL, Dos Santos AA, Zinn FK. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides [Internet]. Journal of Organometallic Chemistry. 2008 ; 693( 17): 2929-2936.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
    • Vancouver

      Comasseto JV, Gariani RA, Princival JL, Dos Santos AA, Zinn FK. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides [Internet]. Journal of Organometallic Chemistry. 2008 ; 693( 17): 2929-2936.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
  • Source: Abstracts. Conference titles: Tetrahedron Symposium - Challenges in Organic Chemistry. Unidades: IQ, IQSC

    Assunto: SÍNTESE ORGÂNICA

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      SILVA JUNIOR, Luiz Fernando da e CRAVEIRO, Marcus Vinicius e GAMBARDELLA, Maria Teresa do Prado. Synthesis of cyclopenta[g]indole derivatives using a thallium(III)-mediated ring contraction reaction. 2007, Anais.. Switzerland: Schweizerische Chemische Gesellschaft (SCG), 2007. . Acesso em: 02 out. 2024.
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      Silva Junior, L. F. da, Craveiro, M. V., & Gambardella, M. T. do P. (2007). Synthesis of cyclopenta[g]indole derivatives using a thallium(III)-mediated ring contraction reaction. In Abstracts. Switzerland: Schweizerische Chemische Gesellschaft (SCG).
    • NLM

      Silva Junior LF da, Craveiro MV, Gambardella MT do P. Synthesis of cyclopenta[g]indole derivatives using a thallium(III)-mediated ring contraction reaction. Abstracts. 2007 ;[citado 2024 out. 02 ]
    • Vancouver

      Silva Junior LF da, Craveiro MV, Gambardella MT do P. Synthesis of cyclopenta[g]indole derivatives using a thallium(III)-mediated ring contraction reaction. Abstracts. 2007 ;[citado 2024 out. 02 ]
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step. Journal of Organometallic Chemistry, v. 689, n. 22, p. 3631-3636, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2004.08.041. Acesso em: 02 out. 2024.
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      Cunha, R. L. O. R., Omori, Á. T., Castelani, P., Toledo, F. T., & Comasseto, J. V. (2004). One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step. Journal of Organometallic Chemistry, 689( 22), 3631-3636. doi:10.1016/j.jorganchem.2004.08.041
    • NLM

      Cunha RLOR, Omori ÁT, Castelani P, Toledo FT, Comasseto JV. One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step [Internet]. Journal of Organometallic Chemistry. 2004 ; 689( 22): 3631-3636.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2004.08.041
    • Vancouver

      Cunha RLOR, Omori ÁT, Castelani P, Toledo FT, Comasseto JV. One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step [Internet]. Journal of Organometallic Chemistry. 2004 ; 689( 22): 3631-3636.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2004.08.041
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      BARRIENTOS-ASTIGARRAGA, Rafael E. et al. Carbon-carbon bond formation by means of organotellurium compounds. Journal of Organometallic Chemistry, v. 623, n. 1-2, p. 43-47, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0022-328x(00)00828-7. Acesso em: 02 out. 2024.
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      Barrientos-Astigarraga, R. E., Castelani, P., Comasseto, J. V., Formiga, H. B., Silva, N. C. da, Sumida, C. Y., & Vieira, M. L. (2001). Carbon-carbon bond formation by means of organotellurium compounds. Journal of Organometallic Chemistry, 623( 1-2), 43-47. doi:10.1016/s0022-328x(00)00828-7
    • NLM

      Barrientos-Astigarraga RE, Castelani P, Comasseto JV, Formiga HB, Silva NC da, Sumida CY, Vieira ML. Carbon-carbon bond formation by means of organotellurium compounds [Internet]. Journal of Organometallic Chemistry. 2001 ; 623( 1-2): 43-47.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0022-328x(00)00828-7
    • Vancouver

      Barrientos-Astigarraga RE, Castelani P, Comasseto JV, Formiga HB, Silva NC da, Sumida CY, Vieira ML. Carbon-carbon bond formation by means of organotellurium compounds [Internet]. Journal of Organometallic Chemistry. 2001 ; 623( 1-2): 43-47.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0022-328x(00)00828-7

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