Filtros : "QUÍMICA ORGÂNICA" "Financiado pela FAPESP" Removido: "ELETROQUÍMICA" Limpar

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  • Source: The Chemical Record. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      DAY, David P e VARGAS, Jorge A. M. e BURTOLOSO, Antonio Carlos Bender. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, v. 21, p. 1-19, 2021Tradução . . Disponível em: https://doi.org/10.1002/tcr.20200017. Acesso em: 05 dez. 2025.
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      Day, D. P., Vargas, J. A. M., & Burtoloso, A. C. B. (2021). Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, 21, 1-19. doi:10.1002/tcr.20200017
    • NLM

      Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/tcr.20200017
    • Vancouver

      Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/tcr.20200017
  • Source: Journal of Molecular Structure. Unidades: IQ, IQSC

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      KHALID, Muhammad et al. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, v. 1230 p. 129827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129827. Acesso em: 05 dez. 2025.
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      Khalid, M., Ali, A., Khan, M. U., Tahir, M. N., Ahmad, A., Ashfaq, M., et al. (2021). Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, 1230 p. 129827. doi:10.1016/j.molstruc.2020.129827
    • NLM

      Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
    • Vancouver

      Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
  • Source: ACS Applied Polymer Materials. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, CELULOSE, BIODEGRADAÇÃO AMBIENTAL

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      KASCHUK, Joice Jaqueline et al. Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices. ACS Applied Polymer Materials, v. 3, n. 5, p. 2393–2401, 2021Tradução . . Disponível em: https://doi.org/10.1021/acsapm.0c01252. Acesso em: 05 dez. 2025.
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      Kaschuk, J. J., Borghei, M., Solin, K., Tripathi, A., Khakalo, A., Leite, F. A. S., et al. (2021). Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices. ACS Applied Polymer Materials, 3( 5), 2393–2401. doi:10.1021/acsapm.0c01252
    • NLM

      Kaschuk JJ, Borghei M, Solin K, Tripathi A, Khakalo A, Leite FAS, Branco A, Sousa MCA de, Frollini E, Rojas OJ. Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices [Internet]. ACS Applied Polymer Materials. 2021 ; 3( 5): 2393–2401.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acsapm.0c01252
    • Vancouver

      Kaschuk JJ, Borghei M, Solin K, Tripathi A, Khakalo A, Leite FAS, Branco A, Sousa MCA de, Frollini E, Rojas OJ. Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices [Internet]. ACS Applied Polymer Materials. 2021 ; 3( 5): 2393–2401.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acsapm.0c01252
  • Source: mBio. Unidades: IQSC, FCF

    Subjects: QUÍMICA ORGÂNICA, FITOPATÓGENOS, FUNGOS, MOFO VERDE

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      COSTA, Jonas Henrique et al. Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles. mBio, v. 12, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1128/mBio.03393-20. Acesso em: 05 dez. 2025.
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      Costa, J. H., Bazioli, J. M., Barbosa, L. D., Santos Júnior, P. L. T. dos, Reis, F. C. G., Klimeck, T., et al. (2021). Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles. mBio, 12( 1). doi:10.1128/mBio.03393-20
    • NLM

      Costa JH, Bazioli JM, Barbosa LD, Santos Júnior PLT dos, Reis FCG, Klimeck T, Crnkovic CM, Berlinck RG de S, Sussulini A, Rodrigues ML, Fill TP. Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles [Internet]. mBio. 2021 ; 12( 1):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1128/mBio.03393-20
    • Vancouver

      Costa JH, Bazioli JM, Barbosa LD, Santos Júnior PLT dos, Reis FCG, Klimeck T, Crnkovic CM, Berlinck RG de S, Sussulini A, Rodrigues ML, Fill TP. Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles [Internet]. mBio. 2021 ; 12( 1):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1128/mBio.03393-20
  • Source: European Journal of Organic Chemistry. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS

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      VARGAS, Jorge Andrés Mora e DAY, David P e BURTOLOSO, Antonio Carlos Bender. Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, v. press, 2021Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202001132. Acesso em: 05 dez. 2025.
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      Vargas, J. A. M., Day, D. P., & Burtoloso, A. C. B. (2021). Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, press. doi:10.1002/ejoc.202001132
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      Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.202001132
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      Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.202001132
  • Source: Chemosphere. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, BACTÉRIAS, PEIXES

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      TONON, Luciane Alessandra Chimetto et al. New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome. Chemosphere, v. 242, p. 125211, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.chemosphere.2019.125211. Acesso em: 05 dez. 2025.
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      Tonon, L. A. C., Azevedo, G. P. R. de, Monteiro, A. F., Bernardi, D. I., Gubiani, J. R., Ióca, L. P., et al. (2020). New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome. Chemosphere, 242, 125211. doi:10.1016/j.chemosphere.2019.125211
    • NLM

      Tonon LAC, Azevedo GPR de, Monteiro AF, Bernardi DI, Gubiani JR, Ióca LP, Mattsson HK, Moreira APB, Gomes AF, Pires Júnior OR, Pedrosa C da SG, Souza LRQ, Rehen SK, Thompson CC, Thompson FL, Berlinck RG de S. New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome [Internet]. Chemosphere. 2020 ; 242 125211.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.chemosphere.2019.125211
    • Vancouver

      Tonon LAC, Azevedo GPR de, Monteiro AF, Bernardi DI, Gubiani JR, Ióca LP, Mattsson HK, Moreira APB, Gomes AF, Pires Júnior OR, Pedrosa C da SG, Souza LRQ, Rehen SK, Thompson CC, Thompson FL, Berlinck RG de S. New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome [Internet]. Chemosphere. 2020 ; 242 125211.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.chemosphere.2019.125211
  • Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, MEDICAMENTO, INIBIDORES DE ENZIMAS

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      MATOS, Thiago Kelvin Brito et al. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB. Bioorganic & Medicinal Chemistry Letters, v. 30, n. 18, p. 127439, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2020.127439. Acesso em: 05 dez. 2025.
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      Matos, T. K. B., Batista, P. H. J., Rocho, F. dos R., Vita, D. de, Pearce, N., Kellam, B., et al. (2020). Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB. Bioorganic & Medicinal Chemistry Letters, 30( 18), 127439. doi:10.1016/j.bmcl.2020.127439
    • NLM

      Matos TKB, Batista PHJ, Rocho F dos R, Vita D de, Pearce N, Kellam B, Montanari CA, Leitão A. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB [Internet]. Bioorganic & Medicinal Chemistry Letters. 2020 ; 30( 18): 127439.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bmcl.2020.127439
    • Vancouver

      Matos TKB, Batista PHJ, Rocho F dos R, Vita D de, Pearce N, Kellam B, Montanari CA, Leitão A. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB [Internet]. Bioorganic & Medicinal Chemistry Letters. 2020 ; 30( 18): 127439.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bmcl.2020.127439
  • Source: Arkivoc. Unidades: FFCLRP, IQ

    Subjects: SAIS, QUÍMICA ORGÂNICA, CONSTANTES QUÍMICAS

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      FREITAS, Adilson A et al. Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins. Arkivoc, p. 146-162, 2020Tradução . . Disponível em: https://doi.org/10.24820/ark.5550190.p011.125. Acesso em: 05 dez. 2025.
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      Freitas, A. A., Shimizu, K., Dias, L. G., & Quina, F. H. (2020). Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins. Arkivoc, 146-162. doi:10.24820/ark.5550190.p011.125
    • NLM

      Freitas AA, Shimizu K, Dias LG, Quina FH. Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins [Internet]. Arkivoc. 2020 ; 146-162.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.125
    • Vancouver

      Freitas AA, Shimizu K, Dias LG, Quina FH. Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins [Internet]. Arkivoc. 2020 ; 146-162.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.125
  • Source: The Journal of Organic Chemistry. Unidade: IQSC

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      CAIUBY, Clarice Alves Dale e JESUS, Matheus Pereira de e BURTOLOSO, Antonio Carlos Bender. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, v. 85, n. 11, p. 7433-7445 April 28, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.0c00833. Acesso em: 05 dez. 2025.
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      Caiuby, C. A. D., Jesus, M. P. de, & Burtoloso, A. C. B. (2020). α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, 85( 11), 7433-7445 April 28. doi:10.1021/acs.joc.0c00833
    • NLM

      Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
    • Vancouver

      Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
  • Source: ARKIVOC - Archive for Organic Chemistry. Unidades: IQ, IQSC

    Subjects: QUÍMICA ORGÂNICA, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      OLIVEIRA, Marcelo Tavares de et al. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds. ARKIVOC - Archive for Organic Chemistry, p. 113-122, 2020Tradução . . Disponível em: https://doi.org/10.24820/ark.5550190.p011.135. Acesso em: 05 dez. 2025.
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      Oliveira, M. T. de, Alves, J. M. A., Morais, S. F. de A., & Braga, A. A. C. (2020). Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds. ARKIVOC - Archive for Organic Chemistry, 113-122. doi:10.24820/ark.5550190.p011.135
    • NLM

      Oliveira MT de, Alves JMA, Morais SF de A, Braga AAC. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds [Internet]. ARKIVOC - Archive for Organic Chemistry. 2020 ; 113-122.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.135
    • Vancouver

      Oliveira MT de, Alves JMA, Morais SF de A, Braga AAC. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds [Internet]. ARKIVOC - Archive for Organic Chemistry. 2020 ; 113-122.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.135
  • Source: Biocatalysis and Agricultural Biotechnology. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, ESTEROIDES, ÁGUA DO MAR

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      PAULA, Samuel Filipe Cardoso de e PORTO, Andre Luiz Meleiro. Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935. Biocatalysis and Agricultural Biotechnology, v. 25, p. 101546, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bcab.2020.101546. Acesso em: 05 dez. 2025.
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      Paula, S. F. C. de, & Porto, A. L. M. (2020). Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935. Biocatalysis and Agricultural Biotechnology, 25, 101546. doi:10.1016/j.bcab.2020.101546
    • NLM

      Paula SFC de, Porto ALM. Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935 [Internet]. Biocatalysis and Agricultural Biotechnology. 2020 ; 25 101546.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bcab.2020.101546
    • Vancouver

      Paula SFC de, Porto ALM. Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935 [Internet]. Biocatalysis and Agricultural Biotechnology. 2020 ; 25 101546.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bcab.2020.101546
  • Source: Organic & Biomolecular Chemistry. Unidade: IQSC

    Assunto: QUÍMICA ORGÂNICA

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      DIAS, Rafael Mafra de Paula e OLIVEIRA, Gabriela P. de e BURTOLOSO, Antonio Carlos Bender. One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds. Organic & Biomolecular Chemistry, v. 18, p. 4815–4823, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0ob00800a. Acesso em: 05 dez. 2025.
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      Dias, R. M. de P., Oliveira, G. P. de, & Burtoloso, A. C. B. (2020). One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds. Organic & Biomolecular Chemistry, 18, 4815–4823. doi:10.1039/d0ob00800a
    • NLM

      Dias RM de P, Oliveira GP de, Burtoloso ACB. One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds [Internet]. Organic & Biomolecular Chemistry. 2020 ;18 4815–4823.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob00800a
    • Vancouver

      Dias RM de P, Oliveira GP de, Burtoloso ACB. One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds [Internet]. Organic & Biomolecular Chemistry. 2020 ;18 4815–4823.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob00800a
  • Source: ChemistrySelect. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, CATALISADORES

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      ZANIN, Lucas Lima e PORTO, Andre 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, v. 5, n. 28, p. 8604-8608, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202001830. Acesso em: 05 dez. 2025.
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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
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      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.[citado 2025 dez. 05 ] 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.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/slct.202001830
  • Source: Organic & Biomolecular Chemistry. Unidade: IQ

    Subjects: ALCALOIDES, QUÍMICA ORGÂNICA

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      NASCIMENTO, Vinicius Rodrigues do e SUENAGA, Melissa Lieko Souza e ANDRADE, Leandro Helgueira. An efficient approach for the synthesis of new (±)-coixspirolactams. Organic & Biomolecular Chemistry, v. 18, p. 5458-5465, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0ob01104e. Acesso em: 05 dez. 2025.
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      Nascimento, V. R. do, Suenaga, M. L. S., & Andrade, L. H. (2020). An efficient approach for the synthesis of new (±)-coixspirolactams. Organic & Biomolecular Chemistry, 18, 5458-5465. doi:10.1039/d0ob01104e
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      Nascimento VR do, Suenaga MLS, Andrade LH. An efficient approach for the synthesis of new (±)-coixspirolactams [Internet]. Organic & Biomolecular Chemistry. 2020 ; 18 5458-5465.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob01104e
    • Vancouver

      Nascimento VR do, Suenaga MLS, Andrade LH. An efficient approach for the synthesis of new (±)-coixspirolactams [Internet]. Organic & Biomolecular Chemistry. 2020 ; 18 5458-5465.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob01104e
  • Source: Current Microbiology. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, GENÔMICA, PEIXES

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      AZEVEDO, Gustavo Pitta Reis de et al. Enterovibrio baiacu sp. nov. Current Microbiology, v. 77, p. 154–157, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00284-019-01785-7. Acesso em: 05 dez. 2025.
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      Azevedo, G. P. R. de, Mattsson, H. K., Appolinario, L. R., Calegario, G., Leomil, L., Walter, J. M., et al. (2020). Enterovibrio baiacu sp. nov. Current Microbiology, 77, 154–157. doi:10.1007/s00284-019-01785-7
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      Azevedo GPR de, Mattsson HK, Appolinario LR, Calegario G, Leomil L, Walter JM, Campeão M, Tonon LAC, Moreira APB, Vidal L, Vieira VV, Otsuki K, Tschoeke DA, Swings J, Thompson FL, Thompson CC. Enterovibrio baiacu sp. nov. [Internet]. Current Microbiology. 2020 ; 77 154–157.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1007/s00284-019-01785-7
    • Vancouver

      Azevedo GPR de, Mattsson HK, Appolinario LR, Calegario G, Leomil L, Walter JM, Campeão M, Tonon LAC, Moreira APB, Vidal L, Vieira VV, Otsuki K, Tschoeke DA, Swings J, Thompson FL, Thompson CC. Enterovibrio baiacu sp. nov. [Internet]. Current Microbiology. 2020 ; 77 154–157.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1007/s00284-019-01785-7
  • Source: Nature Protocols. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      BERNARDIM, Barbara et al. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, v. 14, n. Ja 2019, p. 86-99, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41596-018-0083-9. Acesso em: 05 dez. 2025.
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      Bernardim, B., Matos, M. J., Ferhati, X., Compañón, I., Guerreiro, A., Akkapeddi, P., et al. (2019). Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, 14( Ja 2019), 86-99. doi:10.1038/s41596-018-0083-9
    • NLM

      Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
    • Vancouver

      Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
  • Source: Heliyon. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, QUÍMICA FARMACÊUTICA, TOXICOLOGIA, CARCINOMA HEPATOCELULAR, ADENOCARCINOMA, MAMA

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      QUEIROZ, Thayane M et al. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, v. 5, n. 9, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2019.e02408. Acesso em: 05 dez. 2025.
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      Queiroz, T. M., Orozco, E. V. M., Silva, V., Santos, L. S., Soares, M. B. P., Bezerra, D. P., & Porto, A. L. M. (2019). Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, 5( 9). doi:10.1016/j.heliyon.2019.e02408
    • NLM

      Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
    • Vancouver

      Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
  • Source: Organic letters. Unidade: IQSC

    Assunto: QUÍMICA ORGÂNICA

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      AHMAD, Anees e BURTOLOSO, Antonio Carlos Bender. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, v. 21, p. 6079-6083, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.9b02221. Acesso em: 05 dez. 2025.
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      Ahmad, A., & Burtoloso, A. C. B. (2019). Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, 21, 6079-6083. doi:10.1021/acs.orglett.9b02221
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      Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
    • Vancouver

      Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
  • Source: Biocatalysis and Agricultural Biotechnology. Unidade: IQSC

    Subjects: IRRADIAÇÃO, QUÍMICA ORGÂNICA

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      MORAIS, Aline Teixeira do Brasil et al. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi. Biocatalysis and Agricultural Biotechnology, v. 16. p.314-319, 2018Tradução . . Disponível em: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd. Acesso em: 05 dez. 2025.
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      Morais, A. T. do B., Ferreira , I. M., Jimenez, D. E. Q., & Porto, A. L. M. (2018). Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi. Biocatalysis and Agricultural Biotechnology, 16. p.314-319. doi:10.1016/j.bcab.2018.08.003
    • NLM

      Morais AT do B, Ferreira IM, Jimenez DEQ, Porto ALM. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi [Internet]. Biocatalysis and Agricultural Biotechnology. 2018 ;16. p.314-319[citado 2025 dez. 05 ] Available from: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd
    • Vancouver

      Morais AT do B, Ferreira IM, Jimenez DEQ, Porto ALM. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi [Internet]. Biocatalysis and Agricultural Biotechnology. 2018 ;16. p.314-319[citado 2025 dez. 05 ] Available from: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd
  • Source: Physical Chemistry Chemical Physics. Unidade: FFCLRP

    Subjects: QUÍMICA ORGÂNICA, RUTÊNIO, ÓXIDO NÍTRICO

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      ORENHA, Renato Pereira e TFOUNI, Elia e GALEMBECK, Sérgio Emanuel. How does the total charge and isomerism influence the Ru–NO ammine complexes?. Physical Chemistry Chemical Physics, v. 20, n. 19, p. 13348-13356, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8cp00865e. Acesso em: 05 dez. 2025.
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      Orenha, R. P., Tfouni, E., & Galembeck, S. E. (2018). How does the total charge and isomerism influence the Ru–NO ammine complexes? Physical Chemistry Chemical Physics, 20( 19), 13348-13356. doi:10.1039/c8cp00865e
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      Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/c8cp00865e
    • Vancouver

      Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/c8cp00865e

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