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  • Source: Arkivoc. Unidade: IQ

    Subjects: ANTIRRETROVIRAIS, COMPOSTOS ORGÂNICOS, COMPOSTOS HETEROCÍCLICOS

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    • ABNT

      MOURA, Rebeca Garcia et al. Synthesis of the piperazine subunit of Indinavir. Arkivoc, v. 2021, p. 106-111, 2021Tradução . . Disponível em: https://doi.org/10.24820/ark.5550190.p011.621. Acesso em: 04 out. 2024.
    • APA

      Moura, R. G., Bueno Filho, M. A., Marzorati, L., & Di Vitta, C. (2021). Synthesis of the piperazine subunit of Indinavir. Arkivoc, 2021, 106-111. doi:10.24820/ark.5550190.p011.621
    • NLM

      Moura RG, Bueno Filho MA, Marzorati L, Di Vitta C. Synthesis of the piperazine subunit of Indinavir [Internet]. Arkivoc. 2021 ; 2021 106-111.[citado 2024 out. 04 ] Available from: https://doi.org/10.24820/ark.5550190.p011.621
    • Vancouver

      Moura RG, Bueno Filho MA, Marzorati L, Di Vitta C. Synthesis of the piperazine subunit of Indinavir [Internet]. Arkivoc. 2021 ; 2021 106-111.[citado 2024 out. 04 ] Available from: https://doi.org/10.24820/ark.5550190.p011.621
  • Source: Organic Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS

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      RICHTHOFEN, Andreas Albert Von et al. Synthesis and diels-alder reactions of a benzo[5]radialene derivative. Organic Letters, v. 16, n. 15, p. 4020-4023, 2014Tradução . . Disponível em: https://doi.org/10.1021/ol5018432. Acesso em: 04 out. 2024.
    • APA

      Richthofen, A. A. V., Marzorati, L., Ducati, L. C., & Di Vitta, C. (2014). Synthesis and diels-alder reactions of a benzo[5]radialene derivative. Organic Letters, 16( 15), 4020-4023. doi:10.1021/ol5018432
    • NLM

      Richthofen AAV, Marzorati L, Ducati LC, Di Vitta C. Synthesis and diels-alder reactions of a benzo[5]radialene derivative [Internet]. Organic Letters. 2014 ; 16( 15): 4020-4023.[citado 2024 out. 04 ] Available from: https://doi.org/10.1021/ol5018432
    • Vancouver

      Richthofen AAV, Marzorati L, Ducati LC, Di Vitta C. Synthesis and diels-alder reactions of a benzo[5]radialene derivative [Internet]. Organic Letters. 2014 ; 16( 15): 4020-4023.[citado 2024 out. 04 ] Available from: https://doi.org/10.1021/ol5018432
  • Source: Journal of Lipids. Unidade: IQ

    Subjects: FOSFOLIPÍDEOS, QUÍMICA ORGÂNICA

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    • ABNT

      DI VITTA, Cláudio e MARZORATI, Liliana e FUNARI, Sérgio de Souza. Modification of phospholipid bilayers induced by sulfurated naphthoquinones. Journal of Lipids, p. 1-8 art. ID 592318, 2013Tradução . . Disponível em: https://doi.org/10.1155/2013/592318. Acesso em: 04 out. 2024.
    • APA

      Di Vitta, C., Marzorati, L., & Funari, S. de S. (2013). Modification of phospholipid bilayers induced by sulfurated naphthoquinones. Journal of Lipids, 1-8 art. ID 592318. doi:10.1155/2013/592318
    • NLM

      Di Vitta C, Marzorati L, Funari S de S. Modification of phospholipid bilayers induced by sulfurated naphthoquinones [Internet]. Journal of Lipids. 2013 ; 1-8 art. ID 592318.[citado 2024 out. 04 ] Available from: https://doi.org/10.1155/2013/592318
    • Vancouver

      Di Vitta C, Marzorati L, Funari S de S. Modification of phospholipid bilayers induced by sulfurated naphthoquinones [Internet]. Journal of Lipids. 2013 ; 1-8 art. ID 592318.[citado 2024 out. 04 ] Available from: https://doi.org/10.1155/2013/592318
  • Source: European Biophysics Journal. Conference titles: European Biophysics Congress (EBSA). Unidade: IQ

    Subjects: LIPÍDEOS, SÍNTESE ORGÂNICA

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      FUNARI, Sérgio de Souza et al. Lipid-soluble hydroquinone modifications induced on membranes. European Biophysics Journal. New York: Instituto de Química, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2011
    • APA

      Funari, S. de S., Rebbin, V., Marzorati, L., & Di Vitta, C. (2011). Lipid-soluble hydroquinone modifications induced on membranes. European Biophysics Journal. New York: Instituto de Química, Universidade de São Paulo.
    • NLM

      Funari S de S, Rebbin V, Marzorati L, Di Vitta C. Lipid-soluble hydroquinone modifications induced on membranes. European Biophysics Journal. 2011 ; 40 S197 res. P-605.[citado 2024 out. 04 ]
    • Vancouver

      Funari S de S, Rebbin V, Marzorati L, Di Vitta C. Lipid-soluble hydroquinone modifications induced on membranes. European Biophysics Journal. 2011 ; 40 S197 res. P-605.[citado 2024 out. 04 ]
  • Source: Journal of Labelled Compounds & Radiopharmaceuticals. Conference titles: International Symposium on Radiopharmaceutical Sciences. Unidades: FM, IQ

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      MARQUES, Fabio Luiz Navarro et al. Synthesis and characterization of new ligands and complexes [['ANTPOT. 99M'TC](MeOBzTriN)(CO)'IND. 3']'POT. +'. Journal of Labelled Compounds & Radiopharmaceuticals. Malden: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2011
    • APA

      Marques, F. L. N., Luz, C. P., Di Vitta, C., & Buchpiguel, C. A. (2011). Synthesis and characterization of new ligands and complexes [['ANTPOT. 99M'TC](MeOBzTriN)(CO)'IND. 3']'POT. +'. Journal of Labelled Compounds & Radiopharmaceuticals. Malden: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Marques FLN, Luz CP, Di Vitta C, Buchpiguel CA. Synthesis and characterization of new ligands and complexes [['ANTPOT. 99M'TC](MeOBzTriN)(CO)'IND. 3']'POT. +'. Journal of Labelled Compounds & Radiopharmaceuticals. 2011 ; 54 S395 res. P-306.[citado 2024 out. 04 ]
    • Vancouver

      Marques FLN, Luz CP, Di Vitta C, Buchpiguel CA. Synthesis and characterization of new ligands and complexes [['ANTPOT. 99M'TC](MeOBzTriN)(CO)'IND. 3']'POT. +'. Journal of Labelled Compounds & Radiopharmaceuticals. 2011 ; 54 S395 res. P-306.[citado 2024 out. 04 ]
  • Source: Langmuir. Unidade: IQ

    Subjects: COLESTEROL, QUÍMICA ORGÂNICA

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      FUNARI, Sérgio de Souza et al. Membrane morphology modifications induced by hydroquinones. Langmuir, v. 27, n. 13, p. 8257-8262, 2011Tradução . . Disponível em: https://doi.org/10.1021/la200768x. Acesso em: 04 out. 2024.
    • APA

      Funari, S. de S., Rebbin, V., Marzorati, L., & Di Vitta, C. (2011). Membrane morphology modifications induced by hydroquinones. Langmuir, 27( 13), 8257-8262. doi:10.1021/la200768x
    • NLM

      Funari S de S, Rebbin V, Marzorati L, Di Vitta C. Membrane morphology modifications induced by hydroquinones [Internet]. Langmuir. 2011 ; 27( 13): 8257-8262.[citado 2024 out. 04 ] Available from: https://doi.org/10.1021/la200768x
    • Vancouver

      Funari S de S, Rebbin V, Marzorati L, Di Vitta C. Membrane morphology modifications induced by hydroquinones [Internet]. Langmuir. 2011 ; 27( 13): 8257-8262.[citado 2024 out. 04 ] Available from: https://doi.org/10.1021/la200768x
  • Source: Acta Crystallographica. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, REAÇÕES ORGÂNICAS

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    • ABNT

      RICHTHOFEN, Andreas Albert Von et al. 5-Methyl-2,4-bis(methylsulfanyl)-tricyclo'[6.2.1.0 POT. 2,7]'undeca-4,9-diene-3,6-'dione POT. 1'. Acta Crystallographica, v. E66, p. 01259 : + Supplementary materials ( S1-S7), 2010Tradução . . Disponível em: https://doi.org/10.1107/s1600536810015710. Acesso em: 04 out. 2024.
    • APA

      Richthofen, A. A. V., Cardoso Filho, J. E. P., Marzorati, L., Zukerman-Schpector, J., Tiekink, E. R. T., & Di Vitta, C. (2010). 5-Methyl-2,4-bis(methylsulfanyl)-tricyclo'[6.2.1.0 POT. 2,7]'undeca-4,9-diene-3,6-'dione POT. 1'. Acta Crystallographica, E66, 01259 : + Supplementary materials ( S1-S7). doi:10.1107/s1600536810015710
    • NLM

      Richthofen AAV, Cardoso Filho JEP, Marzorati L, Zukerman-Schpector J, Tiekink ERT, Di Vitta C. 5-Methyl-2,4-bis(methylsulfanyl)-tricyclo'[6.2.1.0 POT. 2,7]'undeca-4,9-diene-3,6-'dione POT. 1' [Internet]. Acta Crystallographica. 2010 ; E66 01259 : + Supplementary materials ( S1-S7).[citado 2024 out. 04 ] Available from: https://doi.org/10.1107/s1600536810015710
    • Vancouver

      Richthofen AAV, Cardoso Filho JEP, Marzorati L, Zukerman-Schpector J, Tiekink ERT, Di Vitta C. 5-Methyl-2,4-bis(methylsulfanyl)-tricyclo'[6.2.1.0 POT. 2,7]'undeca-4,9-diene-3,6-'dione POT. 1' [Internet]. Acta Crystallographica. 2010 ; E66 01259 : + Supplementary materials ( S1-S7).[citado 2024 out. 04 ] Available from: https://doi.org/10.1107/s1600536810015710
  • Source: Organic Preparations and Procedures International. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      WLADISLAW, Blanka e MARZORATI, Liliana e DI VITTA, Cláudio. Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International, v. 39, n. 5, p. 447-494, 2007Tradução . . Acesso em: 04 out. 2024.
    • APA

      Wladislaw, B., Marzorati, L., & Di Vitta, C. (2007). Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International, 39( 5), 447-494.
    • NLM

      Wladislaw B, Marzorati L, Di Vitta C. Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International. 2007 ; 39( 5): 447-494.[citado 2024 out. 04 ]
    • Vancouver

      Wladislaw B, Marzorati L, Di Vitta C. Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International. 2007 ; 39( 5): 447-494.[citado 2024 out. 04 ]
  • Source: Biophysical Journal. Conference titles: Annual Meeting of the Biophysical Society. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA

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    • ABNT

      FUNARI, Sérgio de Souza e HANULOVA, Maria e DI VITTA, Cláudio. Interaction of long side chains Quinones and hydroquinones with model membranes. Biophysical Journal. Bethesda: Instituto de Química, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 2007
    • APA

      Funari, S. de S., Hanulova, M., & Di Vitta, C. (2007). Interaction of long side chains Quinones and hydroquinones with model membranes. Biophysical Journal. Bethesda: Instituto de Química, Universidade de São Paulo.
    • NLM

      Funari S de S, Hanulova M, Di Vitta C. Interaction of long side chains Quinones and hydroquinones with model membranes. Biophysical Journal. 2007 ;[citado 2024 out. 04 ]
    • Vancouver

      Funari S de S, Hanulova M, Di Vitta C. Interaction of long side chains Quinones and hydroquinones with model membranes. Biophysical Journal. 2007 ;[citado 2024 out. 04 ]
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS

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      WLADISLAW, Blanka et al. Phase transfer catalysis (PTC) sulfanylation of some 2-methylsulfinyl-cyclanones. Journal of Organic Chemistry, v. 69, n. 26, p. 9296-9298, 2004Tradução . . Acesso em: 04 out. 2024.
    • APA

      Wladislaw, B., Bueno, M. A., Marzorati, L., Di Vitta, C., & Zukerman-Schpector, J. (2004). Phase transfer catalysis (PTC) sulfanylation of some 2-methylsulfinyl-cyclanones. Journal of Organic Chemistry, 69( 26), 9296-9298.
    • NLM

      Wladislaw B, Bueno MA, Marzorati L, Di Vitta C, Zukerman-Schpector J. Phase transfer catalysis (PTC) sulfanylation of some 2-methylsulfinyl-cyclanones. Journal of Organic Chemistry. 2004 ; 69( 26): 9296-9298.[citado 2024 out. 04 ]
    • Vancouver

      Wladislaw B, Bueno MA, Marzorati L, Di Vitta C, Zukerman-Schpector J. Phase transfer catalysis (PTC) sulfanylation of some 2-methylsulfinyl-cyclanones. Journal of Organic Chemistry. 2004 ; 69( 26): 9296-9298.[citado 2024 out. 04 ]
  • Source: Phosphorus, Sulfur, and Silicon and the Related Elements. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, ALQUILAÇÃO

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      WLADISLAW, Blanka et al. Reaction of alpha-benzenesulfonylphenylacetic acid with alkyl halides. Decarboxylative alkylation vs. decarboxylative protonation. Phosphorus, Sulfur, and Silicon and the Related Elements, v. 179, n. 7, p. 1403-1409, 2004Tradução . . Acesso em: 04 out. 2024.
    • APA

      Wladislaw, B., Perna, F., Neves, R. M. de A., Marzorati, L., & Di Vitta, C. (2004). Reaction of alpha-benzenesulfonylphenylacetic acid with alkyl halides. Decarboxylative alkylation vs. decarboxylative protonation. Phosphorus, Sulfur, and Silicon and the Related Elements, 179( 7), 1403-1409.
    • NLM

      Wladislaw B, Perna F, Neves RM de A, Marzorati L, Di Vitta C. Reaction of alpha-benzenesulfonylphenylacetic acid with alkyl halides. Decarboxylative alkylation vs. decarboxylative protonation. Phosphorus, Sulfur, and Silicon and the Related Elements. 2004 ; 179( 7): 1403-1409.[citado 2024 out. 04 ]
    • Vancouver

      Wladislaw B, Perna F, Neves RM de A, Marzorati L, Di Vitta C. Reaction of alpha-benzenesulfonylphenylacetic acid with alkyl halides. Decarboxylative alkylation vs. decarboxylative protonation. Phosphorus, Sulfur, and Silicon and the Related Elements. 2004 ; 179( 7): 1403-1409.[citado 2024 out. 04 ]
  • Source: Synthetic Communications. Unidade: IQ

    Assunto: REAÇÕES ORGÂNICAS

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      MARZORATI, Liliana et al. PTC sulfanylation of arylacetates. Synthetic Communications, v. 33, n. 20, p. 3491-3495, 2003Tradução . . Acesso em: 04 out. 2024.
    • APA

      Marzorati, L., Silva, M. A. da, Wladislaw, B., & Di Vitta, C. (2003). PTC sulfanylation of arylacetates. Synthetic Communications, 33( 20), 3491-3495.
    • NLM

      Marzorati L, Silva MA da, Wladislaw B, Di Vitta C. PTC sulfanylation of arylacetates. Synthetic Communications. 2003 ; 33( 20): 3491-3495.[citado 2024 out. 04 ]
    • Vancouver

      Marzorati L, Silva MA da, Wladislaw B, Di Vitta C. PTC sulfanylation of arylacetates. Synthetic Communications. 2003 ; 33( 20): 3491-3495.[citado 2024 out. 04 ]
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: CATÁLISE, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      MARZORATI, Liliana et al. Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications, v. 32, n. 9, p. 1427-1435, 2002Tradução . . Acesso em: 04 out. 2024.
    • APA

      Marzorati, L., Mattos, M. C. de, Wladislaw, B., & Di Vitta, C. (2002). Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications, 32( 9), 1427-1435.
    • NLM

      Marzorati L, Mattos MC de, Wladislaw B, Di Vitta C. Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications. 2002 ; 32( 9): 1427-1435.[citado 2024 out. 04 ]
    • Vancouver

      Marzorati L, Mattos MC de, Wladislaw B, Di Vitta C. Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications. 2002 ; 32( 9): 1427-1435.[citado 2024 out. 04 ]
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, FÍSICO-QUÍMICA, CATÁLISE, ALQUILAÇÃO

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      WLADISLAW, Blanka et al. Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications, v. 32, n. 10, p. 1483-1487, 2002Tradução . . Acesso em: 04 out. 2024.
    • APA

      Wladislaw, B., Marzorati, L., Neves, R. M. A., & Di Vitta, C. (2002). Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications, 32( 10), 1483-1487.
    • NLM

      Wladislaw B, Marzorati L, Neves RMA, Di Vitta C. Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications. 2002 ; 32( 10): 1483-1487.[citado 2024 out. 04 ]
    • Vancouver

      Wladislaw B, Marzorati L, Neves RMA, Di Vitta C. Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications. 2002 ; 32( 10): 1483-1487.[citado 2024 out. 04 ]
  • Source: Phosphorus Sulfur and Silicon and the Related Elements. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      WLADISLAW, Blanka et al. New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements, v. 161, p. 1-7, 2000Tradução . . Acesso em: 04 out. 2024.
    • APA

      Wladislaw, B., Marzorati, L., Di Vitta, C., & Claro Júnior, N. F. (2000). New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements, 161, 1-7.
    • NLM

      Wladislaw B, Marzorati L, Di Vitta C, Claro Júnior NF. New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements. 2000 ; 161 1-7.[citado 2024 out. 04 ]
    • Vancouver

      Wladislaw B, Marzorati L, Di Vitta C, Claro Júnior NF. New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements. 2000 ; 161 1-7.[citado 2024 out. 04 ]
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, ENXOFRE

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      DI VITTA, Cláudio e WLADISLAW, Blanka e MARZORATI, Liliana. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications, v. 30, n. 18, p. 3413-3422, 2000Tradução . . Acesso em: 04 out. 2024.
    • APA

      Di Vitta, C., Wladislaw, B., & Marzorati, L. (2000). Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications, 30( 18), 3413-3422.
    • NLM

      Di Vitta C, Wladislaw B, Marzorati L. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications. 2000 ; 30( 18): 3413-3422.[citado 2024 out. 04 ]
    • Vancouver

      Di Vitta C, Wladislaw B, Marzorati L. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications. 2000 ; 30( 18): 3413-3422.[citado 2024 out. 04 ]
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      CARREÑO, M C e URBANO, Antonio e DI VITTA, Cláudio. Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry, v. 63, n. 23, p. 8320-8330, 1998Tradução . . Acesso em: 04 out. 2024.
    • APA

      Carreño, M. C., Urbano, A., & Di Vitta, C. (1998). Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry, 63( 23), 8320-8330.
    • NLM

      Carreño MC, Urbano A, Di Vitta C. Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry. 1998 ; 63( 23): 8320-8330.[citado 2024 out. 04 ]
    • Vancouver

      Carreño MC, Urbano A, Di Vitta C. Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry. 1998 ; 63( 23): 8320-8330.[citado 2024 out. 04 ]

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