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Filtros : "FCF004" "Shamim, Anwar" Removidos: "Estudos Avançados" "República Tcheca" "ENSINO CIÊNCIAS" Limpar

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  • Artigo de periodico

    Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study (2021)

    Veloso, Rodolpho Rebello; Shamim, Anwar ; Lamarre, Yann Ives; Stefani, Hélio Alexandre ; Sciani, Juliana Mozer

    Source: Bioorganic Chemistry. Unidades: FCF, IQSC, FMRP

    Subjects: ANEMIA FALCIFORME, ANTIOXIDANTES

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      VELOSO, Rodolpho Rebello et al. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, v. 109, p. 104709, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.104709. Acesso em: 20 ago. 2024.

    • APA

      Veloso, R. R., Shamim, A., Lamarre, Y. I., Stefani, H. A., & Sciani, J. M. (2021). Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, 109, 104709. doi:10.1016/j.bioorg.2021.104709

    • NLM

      Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709

    • Vancouver

      Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709

  • Artigo de periodico

    Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones (2019)

    Vasconcelos, Stanley Nunes Siqueira ; Oliveira, Isadora Maria de ; Shamim, Anwar ; Zukerman-Schpector, Júlio ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre

    Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC

    Subjects: ALDEÍDOS, ESTEREOQUÍMICA

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    • ABNT

      VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 20 ago. 2024.

    • APA

      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.[citado 2024 ago. 20 ] Available from: https://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.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1002/adsc.201900564

  • Artigo de periodico

    Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)

    Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre

    Source: Synthesis. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 20 ago. 2024.

    • APA

      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.[citado 2024 ago. 20 ] Available from: https://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.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1055/s-0036-1589090

  • Artigo de periodico

    Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization (2017)

    Shamim, Anwar; Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, COBRE

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      SHAMIM, Anwar et al. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, v. 58, n. 9, p. 884-888, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.059. Acesso em: 20 ago. 2024.

    • 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.[citado 2024 ago. 20 ] Available from: https://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.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059

  • Artigo de periodico

    Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles (2017)

    Ali, Bakhat; Vasconcelos, Stanley N. S; Shamim, Anwar; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre

    Source: Arabian Journal of Chemistry. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS

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      ALI, Bakhat et al. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, v. 10, n. 4, p. 500-508, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.06.003. Acesso em: 20 ago. 2024.

    • APA

      Ali, B., Vasconcelos, S. N. S., Shamim, A., Schpector, J. Z., & Stefani, H. A. (2017). Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, 10( 4), 500-508. doi:10.1016/j.arabjc.2016.06.003

    • NLM

      Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003

    • Vancouver

      Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003

  • Artigo de periodico

    3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)

    Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre

    Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF

    Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS

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      VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 20 ago. 2024.

    • APA

      Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., 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. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154

    • NLM

      Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1002/ajoc.201700154

    • Vancouver

      Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1002/ajoc.201700154

  • Artigo de periodico

    Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines (2017)

    Oliveira, Isadora M. de; Vasconcelos, Stanley S. N; Barbeiro, Cristiane S; Correra, Thiago Carita ; Shamim, Anwar; Pimenta, Daniel Carvalho; Caracelli, Ignez; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia

    Source: New Journal of Chemistry. Unidades: IQ, FCF

    Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS

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      OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 20 ago. 2024.

    • APA

      Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g

    • NLM

      Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1039/c7nj01803g

    • Vancouver

      Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1039/c7nj01803g

  • Artigo de periodico

    Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine (2016)

    Vasconcelos, Stanley Nunes Siqueira; Shamim, Anwar; Ali, Bakhat; Oliveira, Isadora M. de; Stefani, Hélio Alexandre

    Source: Molecular Diversity. Unidade: FCF

    Subjects: PEPTÍDEOS, TIROXINA

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    • ABNT

      VASCONCELOS, Stanley Nunes Siqueira et al. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, v. 20, n. 2, p. 469-481, 2016Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9642-y. Acesso em: 20 ago. 2024.

    • APA

      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.[citado 2024 ago. 20 ] Available from: https://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.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1007/s11030-015-9642-y

  • Artigo de periodico

    Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization (2015)

    Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Ali, Bakhat; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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      SHAMIM, Anwar 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, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 20 ago. 2024.

    • APA

      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.[citado 2024 ago. 20 ] Available from: https://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.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052

  • Artigo de periodico

    Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones (2015)

    Ali, Bakhat; Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      ALI, Bakhat et al. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, v. 56, n. 28, p. 4234-4241, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.05.066. Acesso em: 20 ago. 2024.

    • 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.[citado 2024 ago. 20 ] Available from: https://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.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066

  • Artigo de periodico

    Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes (2015)

    Ali, Bakhat; Schpector, Júlio Zukerman; Ferreira, Fernando P; Shamim, Anwar; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINAS, CATÁLISE

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      ALI, Bakhat et al. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, v. 56, n. 9, p. 1153-1158, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 20 ago. 2024.

    • APA

      Ali, B., Schpector, J. Z., Ferreira, F. P., Shamim, A., Pimenta, D. C., & Stefani, H. A. (2015). Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, 56( 9), 1153-1158. doi:10.1016/j.tetlet.2015.01.059

    • NLM

      Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059

    • Vancouver

      Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059

  • Artigo de periodico

    Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement (2015)

    Souza, Frederico B; Shamim, Anwar; Argomedo, Luiz M. Z; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre

    Source: Molecular Diversity. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS

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      SOUZA, Frederico B et al. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, v. 19, n. 4, p. 773-785, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9619-x. Acesso em: 20 ago. 2024.

    • APA

      Souza, F. B., Shamim, A., Argomedo, L. M. Z., Pimenta, D. C., & Stefani, H. A. (2015). Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, 19( 4), 773-785. doi:10.1007/s11030-015-9619-x

    • NLM

      Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1007/s11030-015-9619-x

    • Vancouver

      Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1007/s11030-015-9619-x

  • Artigo de periodico

    Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal (2015)

    Shamim, Anwar; Souza, Frederico Bernardes de; Trossini, Gustavo Henrique Goulart ; Gatti, Fernando de Moura; Stefani, Hélio Alexandre

    Source: Molecular Diversity. Unidade: FCF

    Subjects: ULTRASSOM, FLUORESCÊNCIA

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    • ABNT

      SHAMIM, Anwar et al. Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal. Molecular Diversity, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11030-014-9564-0. Acesso em: 20 ago. 2024.

    • APA

      Shamim, A., Souza, F. B. de, Trossini, G. H. G., Gatti, F. de M., & Stefani, H. A. (2015). Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal. Molecular Diversity. doi:10.1007/s11030-014-9564-0

    • NLM

      Shamim A, Souza FB de, Trossini GHG, Gatti F de M, Stefani HA. Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal [Internet]. Molecular Diversity. 2015 ;[citado 2024 ago. 20 ] Available from: https://doi.org/10.1007/s11030-014-9564-0

    • Vancouver

      Shamim A, Souza FB de, Trossini GHG, Gatti F de M, Stefani HA. Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal [Internet]. Molecular Diversity. 2015 ;[citado 2024 ago. 20 ] Available from: https://doi.org/10.1007/s11030-014-9564-0
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