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  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: POTÁSSIO, SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, v. 52, n. 33, p. 4256-4261 + Supplementary Materials ( S1-S7), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.04.072. Acesso em: 28 out. 2024.
    • APA

      Stefani, H. A., Vieira, A. S., Amaral, M. F. Z. J., & Cooper, L. (2011). Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, 52( 33), 4256-4261 + Supplementary Materials ( S1-S7). doi:10.1016/j.tetlet.2011.04.072
    • NLM

      Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
    • Vancouver

      Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINOÁCIDOS, SÍNTESE ORGÂNICA

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    • ABNT

      STEFANI, Hélio Alexandre e AMARAL, Monica Franco Zanini Junqueira e JUARISTI, Eusebio. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, v. 52, n. 9, p. 1014-1019, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.12.087. Acesso em: 28 out. 2024.
    • APA

      Stefani, H. A., Amaral, M. F. Z. J., & Juaristi, E. (2011). Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, 52( 9), 1014-1019. doi:10.1016/j.tetlet.2010.12.087
    • NLM

      Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
    • Vancouver

      Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
  • Source: Tetrahedron Letters. Unidades: FCF, IQ

    Subjects: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS

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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: 28 out. 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 out. 28 ] 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 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ULTRASSOM, SÍNTESE ORGÂNICA

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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: 28 out. 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 out. 28 ] 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 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2011.09.004

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