Filtros : "VITTA, CLAUDIO DI" "Inglaterra" Removido: "2002" Limpar

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  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      MARZORATI, Liliana et al. New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, v. 48, n. 37, p. 6509-6513, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.07.054. Acesso em: 29 ago. 2024.
    • APA

      Marzorati, L., Barazzone, G. C., Bueno Filho, M. A., Wladislaw, B., & Di Vitta, C. (2007). New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, 48( 37), 6509-6513. doi:10.1016/j.tetlet.2007.07.054
    • NLM

      Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
    • Vancouver

      Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
  • Source: Journal Chemical Society - Perkin Transactions 1. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      DI VITTA, Cláudio et al. New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione. Journal Chemical Society - Perkin Transactions 1, n. 21, p. 3692-3694, 2000Tradução . . Disponível em: https://doi.org/10.1039/b000575o. Acesso em: 29 ago. 2024.
    • APA

      Di Vitta, C., Campos, I. P. de A., Farah, J. P. S., & Zukerman-Schpector, J. (2000). New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione. Journal Chemical Society - Perkin Transactions 1, ( 21), 3692-3694. doi:10.1039/b000575o
    • NLM

      Di Vitta C, Campos IP de A, Farah JPS, Zukerman-Schpector J. New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione [Internet]. Journal Chemical Society - Perkin Transactions 1. 2000 ;( 21): 3692-3694.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1039/b000575o
    • Vancouver

      Di Vitta C, Campos IP de A, Farah JPS, Zukerman-Schpector J. New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione [Internet]. Journal Chemical Society - Perkin Transactions 1. 2000 ;( 21): 3692-3694.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1039/b000575o
  • Source: Tetrahedron: Asymmetry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      CARREÑO, M C et al. Enantioselective Diels-Alder reactions of chiral racemic acyclic dienes with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone. Tetrahedron: Asymmetry, v. 9, n. 17, p. 2965-2969, 1998Tradução . . Disponível em: https://doi.org/10.1016/s0957-4166(98)00323-1. Acesso em: 29 ago. 2024.
    • APA

      Carreño, M. C., García-Cerrada, S., Urbano, A., & Di Vitta, C. (1998). Enantioselective Diels-Alder reactions of chiral racemic acyclic dienes with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone. Tetrahedron: Asymmetry, 9( 17), 2965-2969. doi:10.1016/s0957-4166(98)00323-1
    • NLM

      Carreño MC, García-Cerrada S, Urbano A, Di Vitta C. Enantioselective Diels-Alder reactions of chiral racemic acyclic dienes with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone [Internet]. Tetrahedron: Asymmetry. 1998 ; 9( 17): 2965-2969.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/s0957-4166(98)00323-1
    • Vancouver

      Carreño MC, García-Cerrada S, Urbano A, Di Vitta C. Enantioselective Diels-Alder reactions of chiral racemic acyclic dienes with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone [Internet]. Tetrahedron: Asymmetry. 1998 ; 9( 17): 2965-2969.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/s0957-4166(98)00323-1

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