Filtros : "Vasconcelos, Stanley Nunes Siqueira" Limpar

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  • Source: Future Medicinal Chemistry. Unidades: FCF, ICB

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

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    • ABNT

      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: 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., Pimenta, D. C., & Stefani, H. A. (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, Pimenta DC, Stefani HA. 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, Pimenta DC, Stefani HA. 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: Medicinal Chemistry. Unidade: FCF

    Subjects: MOLÉCULA, ANTINEOPLÁSICOS

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      VASCONCELOS, Stanley Nunes Siqueira; SCIANI, Juliana Mozer; LISBOA, Nicole Mambeli; STEFANI, Hélio Alexandre. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, Sharjah, v. 14, n. 7, p. 709-714, 2018. Disponível em: < http://dx.doi.org/10.2174/1573406414666180309153142 > DOI: 10.2174/1573406414666180309153142.
    • APA

      Vasconcelos, S. N. S., Sciani, J. M., Lisboa, N. M., & Stefani, H. A. (2018). Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, 14( 7), 709-714. doi:10.2174/1573406414666180309153142
    • NLM

      Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.Available from: http://dx.doi.org/10.2174/1573406414666180309153142
    • Vancouver

      Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.Available from: http://dx.doi.org/10.2174/1573406414666180309153142
  • Source: Synthesis. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SHAMIM, Anwar; VASCONCELOS, Stanley Nunes Siqueira; OLIVEIRA, Isadora Maria de; et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, Stuttgart, v. 49, n. 23, p. 5183-5196, 2017. Disponível em: < http://dx.doi.org/10.1055/s-0036-1589090 > DOI: 10.1055/s-0036-1589090.
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      Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
    • NLM

      Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.Available from: http://dx.doi.org/10.1055/s-0036-1589090
    • Vancouver

      Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.Available from: http://dx.doi.org/10.1055/s-0036-1589090
  • Source: Bioorganic Chemistry. Unidade: FCF

    Subjects: CÉLULAS EPITELIAIS, CÉLULAS-TRONCO

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      ALI, Bakat; KUPA, Léonard de Vinci Kanda; HELUANY, Cíntia Scucuglia; et al. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells. Bioorganic Chemistry, San Diego, v. 72, p. 199-207, 2017. Disponível em: < http://dx.doi.org/10.1016/j.bioorg.2017.04.013 > DOI: 10.1016/j.bioorg.2017.04.013.
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      Ali, B., Kupa, L. de V. K., Heluany, C. S., Drewes, C. C., Vasconcelos, S. N. S., Farsky, S. H. P., & Stefani, H. A. (2017). Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells. Bioorganic Chemistry, 72, 199-207. doi:10.1016/j.bioorg.2017.04.013
    • NLM

      Ali B, Kupa L de VK, Heluany CS, Drewes CC, Vasconcelos SNS, Farsky SHP, Stefani HA. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells [Internet]. Bioorganic Chemistry. 2017 ; 72 199-207.Available from: http://dx.doi.org/10.1016/j.bioorg.2017.04.013
    • Vancouver

      Ali B, Kupa L de VK, Heluany CS, Drewes CC, Vasconcelos SNS, Farsky SHP, Stefani HA. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells [Internet]. Bioorganic Chemistry. 2017 ; 72 199-207.Available from: http://dx.doi.org/10.1016/j.bioorg.2017.04.013
  • Source: ChemistrySelect. Unidade: FCF

    Subjects: PALÁDIO, QUÍMICA FARMACÊUTICA

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    • ABNT

      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.
    • APA

      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: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, COBRE

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    • ABNT

      SHAMIM, Anwar; SOUZA, Frederico Bernardes de; VASCONCELOS, Stanley Nunes Siqueira; STEFANI, Hélio Alexandre. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, Oxford, v. 58, n. 9, p. 884-888, 2017. Disponível em: < http://dx.doi.org/10.1016/j.tetlet.2017.01.059 > DOI: 10.1016/j.tetlet.2017.01.059.
    • APA

      Shamim, A., Souza, F. B. de, Vasconcelos, S. N. S., & Stefani, H. A. (2017). Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, 58( 9), 884-888. doi:10.1016/j.tetlet.2017.01.059
    • NLM

      Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.Available from: http://dx.doi.org/10.1016/j.tetlet.2017.01.059
    • Vancouver

      Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.Available from: http://dx.doi.org/10.1016/j.tetlet.2017.01.059
  • Unidade: FCF

    Subjects: INSUMOS FARMACÊUTICOS, FLUORESCÊNCIA, ANTIMALÁRICOS, CÉLULAS

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      VASCONCELOS, Stanley Nunes Siqueira; STEFANI, Hélio Alexandre. Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias. 2017.Universidade de São Paulo, São Paulo, 2017. Disponível em: < http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/ >.
    • APA

      Vasconcelos, S. N. S., & Stefani, H. A. (2017). Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias. Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/
    • NLM

      Vasconcelos SNS, Stefani HA. Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias [Internet]. 2017 ;Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/
    • Vancouver

      Vasconcelos SNS, Stefani HA. Tirosina, substrato em reações de acoplamento cruzado: síntese de dipeptídeos Tyr-Tyr, heterociclos e investigação da atividade biollógica contra células cancerígenas e parasitárias [Internet]. 2017 ;Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-20122017-144457/
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, COBRE

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      SOUZA, Frederico Bernardes de; VASCONCELOS, Stanley Nunes Siqueira; REIS, Joel Savi dos; PIMENTA, Daniel Carvalho; STEFANI, Hélio Alexandre. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, Oxford, v. 58, n. 11, p. 1057-1060, 2017. Disponível em: < http://dx.doi.org/10.1016/j.tetlet.2017.01.107 > DOI: 10.1016/j.tetlet.2017.01.107.
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      Souza, F. B. de, Vasconcelos, S. N. S., Reis, J. S. dos, Pimenta, D. C., & Stefani, H. A. (2017). Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, 58( 11), 1057-1060. doi:10.1016/j.tetlet.2017.01.107
    • NLM

      Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.Available from: http://dx.doi.org/10.1016/j.tetlet.2017.01.107
    • Vancouver

      Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.Available from: http://dx.doi.org/10.1016/j.tetlet.2017.01.107
  • Source: Abstracts. Conference titles: Tetrahedron Symposium - New Development in Organic Chemistry. Unidades: IQ, FCF

    Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS

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      VASCONCELOS, Stanley Nunes Siqueira; SILVA, Vitor Hugo Menezes da; BRAGA, Ataualpa Albert Carmo; PIMENTA, Daniel Carvalho; STEFANI, Hélio Alexandre. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Anais.. Budapest: Elsevier, 2017.
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      Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. In Abstracts. Budapest: Elsevier.
    • NLM

      Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;
    • Vancouver

      Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;
  • Source: Chemistry Select. Unidades: IQ, FCF

    Subjects: FLUORESCÊNCIA, PEPTÍDEOS

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      VASCONCELOS, Stanley Nunes Siqueira; RODRIGUES, Ana Clara Beltran; BASTOS, Erick Leite; STEFANI, Hélio Alexandre. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives. Chemistry Select, Weinheim, v. 1, n. 6, p. 1287-1291, 2016. Disponível em: < http://dx.doi.org/10.1002/slct.201600319 > DOI: 10.1002/slct.201600319.
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      Vasconcelos, S. N. S., Rodrigues, A. C. B., Bastos, E. L., & Stefani, H. A. (2016). Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives. Chemistry Select, 1( 6), 1287-1291. doi:10.1002/slct.201600319
    • NLM

      Vasconcelos SNS, Rodrigues ACB, Bastos EL, Stefani HA. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives [Internet]. Chemistry Select. 2016 ; 1( 6): 1287-1291.Available from: http://dx.doi.org/10.1002/slct.201600319
    • Vancouver

      Vasconcelos SNS, Rodrigues ACB, Bastos EL, Stefani HA. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives [Internet]. Chemistry Select. 2016 ; 1( 6): 1287-1291.Available from: http://dx.doi.org/10.1002/slct.201600319
  • Source: Molecular Diversity. Unidade: FCF

    Subjects: PEPTÍDEOS, TIROXINA

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      VASCONCELOS, Stanley Nunes Siqueira; SHAMIM, Anwar; ALI, Bakhat; OLIVEIRA, Isadora M. de; STEFANI, Hélio Alexandre. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, Dordrecht, v. 20, n. 2, p. 469-481, 2016. Disponível em: < http://dx.doi.org/10.1007/s11030-015-9642-y > DOI: 10.1007/s11030-015-9642-y.
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      Vasconcelos, S. N. S., Shamim, A., Ali, B., Oliveira, I. M. de, & Stefani, H. A. (2016). Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, 20( 2), 469-481. doi:10.1007/s11030-015-9642-y
    • NLM

      Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.Available from: http://dx.doi.org/10.1007/s11030-015-9642-y
    • Vancouver

      Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.Available from: http://dx.doi.org/10.1007/s11030-015-9642-y
  • 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: European Journal of Medicinal Chemistry. Unidade: FCF

    Assunto: MELANOMA

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      VASCONCELOS, Stanley Nunes Siqueira; DREWES, Carine C; KUPA, Leonard de Vinci Kanda; FARSKY, Sandra Helena Poliselli; STEFANI, Hélio Alexandre. Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines. European Journal of Medicinal Chemistry, Paris, v. 114, p. 1-7, 2016. Disponível em: < http://dx.doi.org/10.1016/j.ejmech.2016.02.062 > DOI: 10.1016/j.ejmech.2016.02.062.
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      Vasconcelos, S. N. S., Drewes, C. C., Kupa, L. de V. K., Farsky, S. H. P., & Stefani, H. A. (2016). Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines. European Journal of Medicinal Chemistry, 114, 1-7. doi:10.1016/j.ejmech.2016.02.062
    • NLM

      Vasconcelos SNS, Drewes CC, Kupa L de VK, Farsky SHP, Stefani HA. Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines [Internet]. European Journal of Medicinal Chemistry. 2016 ; 114 1-7.Available from: http://dx.doi.org/10.1016/j.ejmech.2016.02.062
    • Vancouver

      Vasconcelos SNS, Drewes CC, Kupa L de VK, Farsky SHP, Stefani HA. Evaluation of toxicity on epithelial and tumor cells of biaryl dipeptide tyrosines [Internet]. European Journal of Medicinal Chemistry. 2016 ; 114 1-7.Available from: http://dx.doi.org/10.1016/j.ejmech.2016.02.062
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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      SHAMIM, Anwar; VASCONCELOS, Stanley Nunes Siqueira; ALI, Bakhat; et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, Oxford, v. 56, n. 43, p. 5836-5842, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tetlet.2015.08.052 > DOI: 10.1016/j.tetlet.2015.08.052.
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      Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052
    • NLM

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.Available from: http://dx.doi.org/10.1016/j.tetlet.2015.08.052
    • Vancouver

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.Available from: http://dx.doi.org/10.1016/j.tetlet.2015.08.052
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      ALI, Bakhat; SHAMIM, Anwar; VASCONCELOS, Stanley Nunes Siqueira; STEFANI, Hélio Alexandre. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, Oxford, v. 56, n. 28, p. 4234-4241, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tetlet.2015.05.066 > DOI: 10.1016/j.tetlet.2015.05.066.
    • APA

      Ali, B., Shamim, A., Vasconcelos, S. N. S., & Stefani, H. A. (2015). Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, 56( 28), 4234-4241. doi:10.1016/j.tetlet.2015.05.066
    • NLM

      Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.Available from: http://dx.doi.org/10.1016/j.tetlet.2015.05.066
    • Vancouver

      Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.Available from: http://dx.doi.org/10.1016/j.tetlet.2015.05.066
  • Source: Journal of the Brazilian Chemical Society. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, AMINAS

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      KHAN, Amna N; VASCONCELOS, Stanley Nunes Siqueira; CARRAU, Gonzalo; STEFANI, Hélio Alexandre. Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters. Journal of the Brazilian Chemical Society, São Paulo, v. 26, n. 7, p. 1457-1465, 2015. Disponível em: < http://www.scielo.br/pdf/jbchs/v26n7/0103-5053-jbchs-26-07-1457.pdf > DOI: 10.5935/0103-5053.20150114.
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      Khan, A. N., Vasconcelos, S. N. S., Carrau, G., & Stefani, H. A. (2015). Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters. Journal of the Brazilian Chemical Society, 26( 7), 1457-1465. doi:10.5935/0103-5053.20150114
    • NLM

      Khan AN, Vasconcelos SNS, Carrau G, Stefani HA. Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 7): 1457-1465.Available from: http://www.scielo.br/pdf/jbchs/v26n7/0103-5053-jbchs-26-07-1457.pdf
    • Vancouver

      Khan AN, Vasconcelos SNS, Carrau G, Stefani HA. Microwave-Assisted synthesis of β-1,2,3-Triazolyl-α-amino esters [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 7): 1457-1465.Available from: http://www.scielo.br/pdf/jbchs/v26n7/0103-5053-jbchs-26-07-1457.pdf
  • Source: Journal of the Braziliam Chemical Society. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, BORO, SÍNTESE ORGÂNICA

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      VASCONCELOS, Stanley Nunes Siqueira; BARBEIRO, Cristiane S; KHAN, Amna N; STEFANI, Hélio Alexandre. Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts. Journal of the Braziliam Chemical Society, São Paulo, v. 26, n. 4, p. 765-774, 2015. Disponível em: < http://www.scielo.br/pdf/jbchs/v26n4/0103-5053-jbchs-26-04-0765.pdf > DOI: 10.5935/0103-5053.20150038.
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      Vasconcelos, S. N. S., Barbeiro, C. S., Khan, A. N., & Stefani, H. A. (2015). Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts. Journal of the Braziliam Chemical Society, 26( 4), 765-774. doi:10.5935/0103-5053.20150038
    • NLM

      Vasconcelos SNS, Barbeiro CS, Khan AN, Stefani HA. Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts [Internet]. Journal of the Braziliam Chemical Society. 2015 ; 26( 4): 765-774.Available from: http://www.scielo.br/pdf/jbchs/v26n4/0103-5053-jbchs-26-04-0765.pdf
    • Vancouver

      Vasconcelos SNS, Barbeiro CS, Khan AN, Stefani HA. Synthesis of biphenyl tyrosine via cross-coupling Suzuki-Miyaura reaction using Aryltrifluoroborate Salts [Internet]. Journal of the Braziliam Chemical Society. 2015 ; 26( 4): 765-774.Available from: http://www.scielo.br/pdf/jbchs/v26n4/0103-5053-jbchs-26-04-0765.pdf
  • Source: European Journal of Organic Chemistry. Unidade: FCF

    Subjects: ITÉRBIO, BORO, SÍNTESE ORGÂNICA

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    • ABNT

      STEFANI, Hélio Alexandre; MANARIN, Flávia; KHAN, Amna N; VASCONCELOS, Stanley Nunes Siqueira. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, Weinheim, v. 6, p. 1236-1240, 2014. Disponível em: < http://dx.doi.org/10.1002/ejoc.201301421 > DOI: 10.1002/ejoc.201301421.
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      Stefani, H. A., Manarin, F., Khan, A. N., & Vasconcelos, S. N. S. (2014). Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, 6, 1236-1240. doi:10.1002/ejoc.201301421
    • NLM

      Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.Available from: http://dx.doi.org/10.1002/ejoc.201301421
    • Vancouver

      Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.Available from: http://dx.doi.org/10.1002/ejoc.201301421
  • Source: Molecules. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, SÍNTESE ORGÂNICA

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      SCHPECTOR, Julio Zukermann; MADUREIRA, Lucas Sousa; WULF, Glaudeston Dutra; et al. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, Basel, v. 19, n. 2, p. 1990-2003, 2014. Disponível em: < http://dx.doi.org/10.3390/molecules19021990 > DOI: 10.3390/molecules19021990.
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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.Available from: http://dx.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.Available from: http://dx.doi.org/10.3390/molecules19021990

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