Filtros : "ULTRASSOM" "FCF004" Limpar

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  • Source: Green Techniques for Organic Synthesis and Medicinal Chemistry. Unidade: FCF

    Subjects: ULTRASSOM, REAÇÕES QUÍMICAS

    How to cite
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    • ABNT

      CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasonic reactions. Green Techniques for Organic Synthesis and Medicinal Chemistry. Tradução . Hoboken: John Wiley & Sons, 2018. . . Acesso em: 31 ago. 2024.
    • APA

      Cella, R., & Stefani, H. A. (2018). Ultrasonic reactions. In Green Techniques for Organic Synthesis and Medicinal Chemistry. Hoboken: John Wiley & Sons.
    • NLM

      Cella R, Stefani HA. Ultrasonic reactions. In: Green Techniques for Organic Synthesis and Medicinal Chemistry. Hoboken: John Wiley & Sons; 2018. [citado 2024 ago. 31 ]
    • Vancouver

      Cella R, Stefani HA. Ultrasonic reactions. In: Green Techniques for Organic Synthesis and Medicinal Chemistry. Hoboken: John Wiley & Sons; 2018. [citado 2024 ago. 31 ]
  • Source: Molecular Diversity. Unidade: FCF

    Subjects: ULTRASSOM, FLUORESCÊNCIA

    Acesso à fonteAcesso à fonteDOIHow to cite
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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: 31 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. 31 ] 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. 31 ] Available from: https://doi.org/10.1007/s11030-014-9564-0
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ULTRASSOM, SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      STEFANI, Hélio Alexandre e CANDUZINI, Hugo A e MANARIN, Flávia. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition. Tetrahedron Letters, v. 52, n. 46, p. 6086-6090 : + Supplementary materials ( S1-S10), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.09.004. Acesso em: 31 ago. 2024.
    • APA

      Stefani, H. A., Canduzini, H. A., & Manarin, F. (2011). Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition. Tetrahedron Letters, 52( 46), 6086-6090 : + Supplementary materials ( S1-S10). doi:10.1016/j.tetlet.2011.09.004
    • NLM

      Stefani HA, Canduzini HA, Manarin F. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition [Internet]. Tetrahedron Letters. 2011 ; 52( 46): 6086-6090 : + Supplementary materials ( S1-S10).[citado 2024 ago. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2011.09.004
    • Vancouver

      Stefani HA, Canduzini HA, Manarin F. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition [Internet]. Tetrahedron Letters. 2011 ; 52( 46): 6086-6090 : + Supplementary materials ( S1-S10).[citado 2024 ago. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2011.09.004

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