Filtros : "Stefani, Hélio Alexandre" Limpar

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  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: ANTINEOPLÁSICOS, ANTIPROTOZOÁRIOS, APOPTOSE

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      COSTA, Claudia A; LOPES, Rayssa M; FERRAZ, Letícia Silva; et al. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, Oxford, v. 28, p. 1-13 art. 115511, 2020. Disponível em: < http://dx.doi.org/10.1016/j.bmc.2020.115511 > DOI: 10.1016/j.bmc.2020.115511.
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      Costa, C. A., Lopes, R. M., Ferraz, L. S., Esteves, G. N. N., Di Iorio, J. F., Oliveira, I. M. de, et al. (2020). Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, 28, 1-13 art. 115511. doi:10.1016/j.bmc.2020.115511
    • NLM

      Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T, Souza AA. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.Available from: http://dx.doi.org/10.1016/j.bmc.2020.115511
    • Vancouver

      Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T, Souza AA. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.Available from: http://dx.doi.org/10.1016/j.bmc.2020.115511
  • Source: Dyes and Pigments. Unidades: IQ, FCF

    Subjects: SELÊNIO, PALÁDIO, FLUORESCÊNCIA

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      PAULINO, Antonio Augusto Soares; GIROLDO, Lilian; PRADIE, Noriberto Araújo; et al. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, Oxford, v. 179, p. 1-10 art. 108355, 2020. Disponível em: < https://doi.org/10.1016/j.dyepig.2020.108355 > DOI: 10.1016/j.dyepig.2020.108355.
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      Paulino, A. A. S., Giroldo, L., Pradie, N. A., Reis, J. S. dos, Back, D. F., Braga, A. A. C., et al. (2020). Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, 179, 1-10 art. 108355. doi:10.1016/j.dyepig.2020.108355
    • NLM

      Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.Available from: https://doi.org/10.1016/j.dyepig.2020.108355
    • Vancouver

      Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.Available from: https://doi.org/10.1016/j.dyepig.2020.108355
  • Source: RSC Advances. Unidade: FCF

    Subjects: CATÁLISE, COBRE

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      WILLING, Julia C. Mansano; GRANETTO, Gustavo; REGINATO, Danielly; et al. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions. RSC Advances, Cambridge, v. 10, n. 6, p. 3407-3415, 2020. Disponível em: < http://dx.doi.org/10.1039/c9ra10171c > DOI: 10.1039/c9ra10171c.
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      Willing, J. C. M., Granetto, G., Reginato, D., Dutra, F. R., Poruczinski, E. F., Oliveira, I. M. de, et al. (2020). A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions. RSC Advances, 10( 6), 3407-3415. doi:10.1039/c9ra10171c
    • NLM

      Willing JCM, Granetto G, Reginato D, Dutra FR, Poruczinski EF, Oliveira IM de, Stefani HA, de Campos SD, Campos EA de, Manarin F, Botteselle G. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions [Internet]. RSC Advances. 2020 ; 10( 6): 3407-3415.Available from: http://dx.doi.org/10.1039/c9ra10171c
    • Vancouver

      Willing JCM, Granetto G, Reginato D, Dutra FR, Poruczinski EF, Oliveira IM de, Stefani HA, de Campos SD, Campos EA de, Manarin F, Botteselle G. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions [Internet]. RSC Advances. 2020 ; 10( 6): 3407-3415.Available from: http://dx.doi.org/10.1039/c9ra10171c
  • Source: European Journal of Organic Chemistry. Unidades: FCF, IQ

    Subjects: GLICOSÍDEOS, PALÁDIO

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      DARBEM, Mariana P; ESTEVES, Henrique A; OLIVEIRA, Isadora Maria de; STEFANI, Hélio Alexandre. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, Weinheim, v. 2020, p. 5220–5226, 2020. Disponível em: < http://dx.doi.org/10.1002/ejoc.202000846 > DOI: 10.1002/ejoc.202000846.
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      Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, & Stefani, H. A. (2020). α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 5220–5226. doi:10.1002/ejoc.202000846
    • NLM

      Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.Available from: http://dx.doi.org/10.1002/ejoc.202000846
    • Vancouver

      Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.Available from: http://dx.doi.org/10.1002/ejoc.202000846
  • Source: ChemCatChem. Unidades: BIOTECNOLOGIA, FCF, IQ

    Subjects: PALÁDIO, HIDRÓLISE

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      DARBEM, Mariana P; ESTEVES, Henrique A; OLIVEIRA, Isadora Maria de; PIMENTA, Daniel Carvalho; STEFANI, Hélio Alexandre. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, Weinheim, v. 12, n. 2, p. 576-583, 2020. Disponível em: < https://dx.doi.org/10.1002/cctc.201901403 > DOI: 10.1002/cctc.201901403.
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      Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, Pimenta, D. C., & Stefani, H. A. (2020). Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, 12( 2), 576-583. doi:10.1002/cctc.201901403
    • NLM

      Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.Available from: https://dx.doi.org/10.1002/cctc.201901403
    • Vancouver

      Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.Available from: https://dx.doi.org/10.1002/cctc.201901403
  • Source: ChemCatChem. Unidades: FCF, IQ

    Subjects: LIGANTES, CATALISADORES

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      OLIVEIRA, Isadora Maria de; ESTEVES, Henrique A; DARBEM, Mariana P; et al. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, Weinheim, v. 12, p. 3545–3552, 2020. Disponível em: < http://dx.doi.org/10.1002/cctc.202000395 > DOI: 10.1002/cctc.202000395.
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      Oliveira, I. M. de, Esteves, H. A., Darbem, M. P., Sartorelli, A., Correra, T. C., Oliveira, A. F. R., et al. (2020). Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, 12, 3545–3552. doi:10.1002/cctc.202000395
    • NLM

      Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Stefani HA, Zukerman-Schpector J. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.Available from: http://dx.doi.org/10.1002/cctc.202000395
    • Vancouver

      Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Stefani HA, Zukerman-Schpector J. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.Available from: http://dx.doi.org/10.1002/cctc.202000395
  • Source: Journal of Fluorescence. Unidades: FCF, IPEN

    Subjects: LUMINESCÊNCIA, EURÓPIO, TÉRBIO

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      ALI, Bakhat; STEFANI, Hélio Alexandre; IMRAN, Muhammad; et al. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes. Journal of Fluorescence, New York, v. 30, p. 1345–1355, 2020. Disponível em: < http://dx.doi.org/10.1007/s10895-020-02613-z > DOI: 10.1007/s10895-020-02613-z.
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      Ali, B., Stefani, H. A., Imran, M., Irfan, A., Assiri, M. A., Felinto, M. C. F. da C., et al. (2020). Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes. Journal of Fluorescence, 30, 1345–1355. doi:10.1007/s10895-020-02613-z
    • NLM

      Ali B, Stefani HA, Imran M, Irfan A, Assiri MA, Felinto MCF da C, Khalid M, Al-Sehemi AG. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes [Internet]. Journal of Fluorescence. 2020 ; 30 1345–1355.Available from: http://dx.doi.org/10.1007/s10895-020-02613-z
    • Vancouver

      Ali B, Stefani HA, Imran M, Irfan A, Assiri MA, Felinto MCF da C, Khalid M, Al-Sehemi AG. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes [Internet]. Journal of Fluorescence. 2020 ; 30 1345–1355.Available from: http://dx.doi.org/10.1007/s10895-020-02613-z
  • Source: Synthetic Communications. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, SÍNTESE QUÍMICA

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      BALFOUR, Michael N; SCHPECTOR, Júlio Zukerman; RODRIGUEZ, Maria Jose Davila; et al. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, Philadelphia, v. 49, n. 3, p. 351-358, 2019. Disponível em: < http://dx.doi.org/10.1080/00397911.2018.1545032 > DOI: 10.1080/00397911.2018.1545032.
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      Balfour, M. N., Schpector, J. Z., Rodriguez, M. J. D., Reis, J. S. dos, Esteves, C. H. A., & Stefani, H. A. (2019). Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, 49( 3), 351-358. doi:10.1080/00397911.2018.1545032
    • NLM

      Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.Available from: http://dx.doi.org/10.1080/00397911.2018.1545032
    • Vancouver

      Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.Available from: http://dx.doi.org/10.1080/00397911.2018.1545032
  • Source: Dyes and Pigments. Unidade: FCF

    Subjects: SENSORES ÓPTICOS, SÍNTESE ORGÂNICA

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      SANTOS, Fabiano S; ZANOTTO, Gabriel M; ARGOMEDO, Luiz M. Z; et al. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, Oxford, v. 165, p. 372-382, 2019. Disponível em: < http://dx.doi.org/10.1016/j.dyepig.2019.02.047 > DOI: 10.1016/j.dyepig.2019.02.047.
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      Santos, F. S., Zanotto, G. M., Argomedo, L. M. Z., Darbem, M. P., Gonçalves, P. F. B., Stefani, H. A., & Rodembusch, F. S. (2019). Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, 165, 372-382. doi:10.1016/j.dyepig.2019.02.047
    • NLM

      Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.Available from: http://dx.doi.org/10.1016/j.dyepig.2019.02.047
    • Vancouver

      Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.Available from: http://dx.doi.org/10.1016/j.dyepig.2019.02.047
  • Source: Tetrahedron. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      VASCONCELOS, Stanley N. S; REIS, Joel S; OLIVEIRA, Isadora M. de; BALFOUR, Michael N; STEFANI, Hélio Alexandre. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, Oxford, v. 75, p. 1865-1959, 2019. Disponível em: < http://dx.doi.org/10.1016/j.tet.2019.02.001 > DOI: 10.1016/j.tet.2019.02.001.
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      Vasconcelos, S. N. S., Reis, J. S., Oliveira, I. M. de, Balfour, M. N., & Stefani, H. A. (2019). Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, 75, 1865-1959. doi:10.1016/j.tet.2019.02.001
    • NLM

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.Available from: http://dx.doi.org/10.1016/j.tet.2019.02.001
    • Vancouver

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.Available from: http://dx.doi.org/10.1016/j.tet.2019.02.001
  • Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química/SBQ. Unidade: FCF

    Subjects: STAPHYLOCOCCUS, BACTERICIDAS

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      SANTOS, Milena Noronha dos; OLIVEIRA, Isadora Maria de; MANARIM, Flavia; et al. Antibacterial activity of selenoquinolines against Staphylococcus aureus. Anais.. São Paulo: Sociedade Brasileira de Química/SBQ, 2019.Disponível em: .
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      Santos, M. N. dos, Oliveira, I. M. de, Manarim, F., Stefani, H. A., Wiggers, H. J., & Cheleski, J. (2019). Antibacterial activity of selenoquinolines against Staphylococcus aureus. In Resumos. São Paulo: Sociedade Brasileira de Química/SBQ. Recuperado de http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
    • NLM

      Santos MN dos, Oliveira IM de, Manarim F, Stefani HA, Wiggers HJ, Cheleski J. Antibacterial activity of selenoquinolines against Staphylococcus aureus [Internet]. Resumos. 2019 ;Available from: http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
    • Vancouver

      Santos MN dos, Oliveira IM de, Manarim F, Stefani HA, Wiggers HJ, Cheleski J. Antibacterial activity of selenoquinolines against Staphylococcus aureus [Internet]. Resumos. 2019 ;Available from: http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
  • Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química/SBQ. Unidade: FCF

    Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS

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      PEREIRA, Evelin Fornari; GOMES, Renan Augusto; STEFANI, Hélio Alexandre; TROSSINI, Gustavo Henrique Goulart. New methodology for the synthesis of Sirtuin 2 inhibitor analogues in Trypanosoma cruzi parasites. Anais.. São Paulo: Sociedade Brasileira de Química/SBQ, 2019.Disponível em: .
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      Pereira, E. F., Gomes, R. A., Stefani, H. A., & Trossini, G. H. G. (2019). New methodology for the synthesis of Sirtuin 2 inhibitor analogues in Trypanosoma cruzi parasites. In Resumos. São Paulo: Sociedade Brasileira de Química/SBQ. Recuperado de http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
    • NLM

      Pereira EF, Gomes RA, Stefani HA, Trossini GHG. New methodology for the synthesis of Sirtuin 2 inhibitor analogues in Trypanosoma cruzi parasites [Internet]. Resumos. 2019 ;Available from: http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
    • Vancouver

      Pereira EF, Gomes RA, Stefani HA, Trossini GHG. New methodology for the synthesis of Sirtuin 2 inhibitor analogues in Trypanosoma cruzi parasites [Internet]. Resumos. 2019 ;Available from: http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
  • Source: Abstracts. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology/SBBq. Unidade: FCF

    Subjects: CALCOGÊNIOS, MITOCÔNDRIAS

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      LOPES, Rayssa de Mello; COSTA, Cláudia A. da; RODRIGUES, Tiago; et al. Evaluation of the antitumor potential of newly synthesized4-organoselenium-quinolines. Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq, 2019.Disponível em: .
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      Lopes, R. de M., Costa, C. A. da, Rodrigues, T., Ferraz, L. S., Stefani, H. A., & Oliveira, I. M. de. (2019). Evaluation of the antitumor potential of newly synthesized4-organoselenium-quinolines. In Abstracts. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq. Recuperado de http://www.sbbq.org.br/reuniao/2019/images/Livro_Resumos_2019.pdf
    • NLM

      Lopes R de M, Costa CA da, Rodrigues T, Ferraz LS, Stefani HA, Oliveira IM de. Evaluation of the antitumor potential of newly synthesized4-organoselenium-quinolines [Internet]. Abstracts. 2019 ;Available from: http://www.sbbq.org.br/reuniao/2019/images/Livro_Resumos_2019.pdf
    • Vancouver

      Lopes R de M, Costa CA da, Rodrigues T, Ferraz LS, Stefani HA, Oliveira IM de. Evaluation of the antitumor potential of newly synthesized4-organoselenium-quinolines [Internet]. Abstracts. 2019 ;Available from: http://www.sbbq.org.br/reuniao/2019/images/Livro_Resumos_2019.pdf
  • Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC

    Subjects: ALDEÍDOS, ESTEREOQUÍMICA

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      VASCONCELOS, Stanley Nunes Siqueira; OLIVEIRA, Isadora Maria de; SHAMIM, Anwar; et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, Weinheim, v. 361, p. 4243-4254, 2019. Disponível em: < http://dx.doi.org/10.1002/adsc.201900564 > DOI: 10.1002/adsc.201900564.
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      Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Stefani, H. A., & Pimenta, D. C. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564
    • NLM

      Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Stefani HA, Pimenta DC. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.Available from: http://dx.doi.org/10.1002/adsc.201900564
    • Vancouver

      Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Stefani HA, Pimenta DC. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.Available from: http://dx.doi.org/10.1002/adsc.201900564
  • Source: Synthetic Communications. Unidade: FCF

    Subjects: PALÁDIO, COMPOSTOS HETEROCÍCLICOS

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      REIS, Joel Savi dos; CARACELLI, Ignez; SCHPECTOR, Júlio Zukerman; STEFANI, Hélio Alexandre. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, Philadelphia, v. 49, n. 10, p. 1252-1261, 2019. Disponível em: < http://dx.doi.org/10.1080/00397911.2019.1595657 > DOI: 10.1080/00397911.2019.1595657.
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      Reis, J. S. dos, Caracelli, I., Schpector, J. Z., & Stefani, H. A. (2019). Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, 49( 10), 1252-1261. doi:10.1080/00397911.2019.1595657
    • NLM

      Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.Available from: http://dx.doi.org/10.1080/00397911.2019.1595657
    • Vancouver

      Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.Available from: http://dx.doi.org/10.1080/00397911.2019.1595657
  • Source: Future Medicinal Chemistry. Unidades: FCF, ICB

    Subjects: MALÁRIA, PLASMODIUM FALCIPARUM, PROTOZOA, ANTIMALÁRICOS, ANIMAIS PARASITOS, VIRULÊNCIA

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      VASCONCELOS, Stanley Nunes Siqueira; MEISSNER, Kamila Anna; FERRAZ, Witor R.; et al. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum. Future Medicinal Chemistry, London, v. 11, n. 6, p. 525-538, 2019. Disponível em: < http://dx.doi.org/10.4155/fmc-2018-0246 > DOI: 10.4155/fmc-2018-0246.
    • APA

      Vasconcelos, S. N. S., Meissner, K. A., Ferraz, W. R., Trossini, G. H. G., Wrenger, C., & Stefani, H. A. (2019). Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum. Future Medicinal Chemistry, 11( 6), 525-538. doi:10.4155/fmc-2018-0246
    • NLM

      Vasconcelos SNS, Meissner KA, Ferraz WR, Trossini GHG, Wrenger C, Stefani HA. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum [Internet]. Future Medicinal Chemistry. 2019 ; 11( 6): 525-538.Available from: http://dx.doi.org/10.4155/fmc-2018-0246
    • Vancouver

      Vasconcelos SNS, Meissner KA, Ferraz WR, Trossini GHG, Wrenger C, Stefani HA. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum [Internet]. Future Medicinal Chemistry. 2019 ; 11( 6): 525-538.Available from: http://dx.doi.org/10.4155/fmc-2018-0246
  • Source: Resumos. Conference titles: Reunião Anual da Federação de Sociedades de Biologia Experimental/FeSBE. Unidade: FCF

    Subjects: CALCOGÊNIOS, LEISHMANIA MEXICANA

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      IORIO, J. F. D; STEFANI, Hélio Alexandre; RODRIGUES, T; JUDICE, Wagner Alves de Souza. Effects of chalcogenoquinolones in modulation of the activity of cysteine proteases from Leishmania mexicana. Anais.. São Paulo: FeSBE, 2019.Disponível em: .
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      Iorio, J. F. D., Stefani, H. A., Rodrigues, T., & Judice, W. A. de S. (2019). Effects of chalcogenoquinolones in modulation of the activity of cysteine proteases from Leishmania mexicana. In Resumos. São Paulo: FeSBE. Recuperado de http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
    • NLM

      Iorio JFD, Stefani HA, Rodrigues T, Judice WA de S. Effects of chalcogenoquinolones in modulation of the activity of cysteine proteases from Leishmania mexicana [Internet]. Resumos. 2019 ;Available from: http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
    • Vancouver

      Iorio JFD, Stefani HA, Rodrigues T, Judice WA de S. Effects of chalcogenoquinolones in modulation of the activity of cysteine proteases from Leishmania mexicana [Internet]. Resumos. 2019 ;Available from: http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
  • Source: Resumos. Conference titles: Reunião Anual da Federação de Sociedades de Biologia Experimental/FeSBE. Unidade: FCF

    Subjects: COMPOSTOS ORGÂNICOS, SÍNTESE ORGÂNICA

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      FERRAZ, L. S; OLIVEIRA, Isadora Maria de; STEFANI, Hélio Alexandre; RODRIGUES, T. CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline. Anais.. São Paulo: FeSBE, 2019.Disponível em: .
    • APA

      Ferraz, L. S., Oliveira, I. M. de, Stefani, H. A., & Rodrigues, T. (2019). CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline. In Resumos. São Paulo: FeSBE. Recuperado de http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
    • NLM

      Ferraz LS, Oliveira IM de, Stefani HA, Rodrigues T. CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline [Internet]. Resumos. 2019 ;Available from: http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
    • Vancouver

      Ferraz LS, Oliveira IM de, Stefani HA, Rodrigues T. CA2+-dependent mitochondrial permeabilization promoted by 4-organoselenium quinoline [Internet]. Resumos. 2019 ;Available from: http://www2.fesbe.org.br/wp-content/uploads/programa_2019_08_30_comp.pdf
  • Source: RSC Advances. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      DARBEM, Mariana P; ESTEVES, C. Henrique A; OLIVEIRA, Isadora M. de; et al. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, Cambridge, v. 9, p. 9468–9474, 2019. Disponível em: < http://dx.doi.org/10.1039/c9ra00523d > DOI: 10.1039/c9ra00523d.
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      Darbem, M. P., Esteves, C. H. A., Oliveira, I. M. de, Reis, J. S., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, 9, 9468–9474. doi:10.1039/c9ra00523d
    • NLM

      Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.Available from: http://dx.doi.org/10.1039/c9ra00523d
    • Vancouver

      Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.Available from: http://dx.doi.org/10.1039/c9ra00523d
  • Source: European Journal of Organic Chemistry. Unidades: BIOTECNOLOGIA, FCF

    Subjects: MONÓXIDO DE CARBONO, PALÁDIO

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      ESTEVES, Henrique A; DARBEM, Mariana P; PIMENTA, Daniel Carvalho; STEFANI, Hélio Alexandre. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, Weinheim, v. 2019, p. 7384-7388, 2019. Disponível em: < http://dx.doi.org/ 10.1002/ejoc.201901081 > DOI: 10.1002/ejoc.201901081.
    • APA

      Esteves, H. A., Darbem, M. P., Pimenta, D. C., & Stefani, H. A. (2019). Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, 2019, 7384-7388. doi:10.1002/ejoc.201901081
    • NLM

      Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.Available from: http://dx.doi.org/ 10.1002/ejoc.201901081
    • Vancouver

      Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.Available from: http://dx.doi.org/ 10.1002/ejoc.201901081

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