Filtros : "COMPOSTOS HETEROCÍCLICOS" "QUÍMICA VERDE" Limpar

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  • Source: Current Bioactive Compounds. Unidades: IQSC, BIOENGENHARIA

    Subjects: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS, BACTERICIDAS, NEOPLASIAS, CATÁLISE

    PrivadoAcesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      ZANIN, Lucas Lima et al. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties. Current Bioactive Compounds, v. 18, n. 4, p. e191121198117, 2022Tradução . . Disponível em: https://doi.org/10.2174/1573407217666211119092038. Acesso em: 10 jun. 2024.
    • APA

      Zanin, L. L., Jimenez, D. E. Q., Birolli, W. G., Venâncio, T., Valdes, T. A., Leitão, A., & Porto, A. L. M. (2022). Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties. Current Bioactive Compounds, 18( 4), e191121198117. doi:10.2174/1573407217666211119092038
    • NLM

      Zanin LL, Jimenez DEQ, Birolli WG, Venâncio T, Valdes TA, Leitão A, Porto ALM. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties [Internet]. Current Bioactive Compounds. 2022 ; 18( 4): e191121198117.[citado 2024 jun. 10 ] Available from: https://doi.org/10.2174/1573407217666211119092038
    • Vancouver

      Zanin LL, Jimenez DEQ, Birolli WG, Venâncio T, Valdes TA, Leitão A, Porto ALM. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties [Internet]. Current Bioactive Compounds. 2022 ; 18( 4): e191121198117.[citado 2024 jun. 10 ] Available from: https://doi.org/10.2174/1573407217666211119092038
  • Source: Tetrahedron Letters. Unidades: FCF, IQ

    Subjects: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      STEFANI, Hélio Alexandre et al. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, v. 52, n. 51, p. 6883-6886 : + Supplementary materials ( S1-S6), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.10.011. Acesso em: 10 jun. 2024.
    • APA

      Stefani, H. A., Amaral, M. F. Z. J., Manarin, F., Ando, R. A., Silva, N. C. S., & Juaristi, E. (2011). Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, 52( 51), 6883-6886 : + Supplementary materials ( S1-S6). doi:10.1016/j.tetlet.2011.10.011
    • NLM

      Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
    • Vancouver

      Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011

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