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  • Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      ROSSET, Isac George et al. Three-step synthesis of (+ )-preussin from decanal. Journal Organic Chemistry, v. 79, n. 14, p. 6748-6753, 2014Tradução . . Disponível em: https://doi.org/10.1021/jo5011558. Acesso em: 02 maio 2024.
    • APA

      Rosset, I. G., Dias, R. M. de P., Pinho, V. D., & Burtoloso, A. C. B. (2014). Three-step synthesis of (+ )-preussin from decanal. Journal Organic Chemistry, 79( 14), 6748-6753. doi:10.1021/jo5011558
    • NLM

      Rosset IG, Dias RM de P, Pinho VD, Burtoloso ACB. Three-step synthesis of (+ )-preussin from decanal [Internet]. Journal Organic Chemistry. 2014 ; 79( 14): 6748-6753.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo5011558
    • Vancouver

      Rosset IG, Dias RM de P, Pinho VD, Burtoloso ACB. Three-step synthesis of (+ )-preussin from decanal [Internet]. Journal Organic Chemistry. 2014 ; 79( 14): 6748-6753.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo5011558
  • Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      ROSSET, Isac George e BURTOLOSO, Antonio Carlos Bender. Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones. Journal Organic Chemistry, v. 78, p. 9464-9470, 2013Tradução . . Disponível em: https://doi.org/10.1021/jo401191s. Acesso em: 02 maio 2024.
    • APA

      Rosset, I. G., & Burtoloso, A. C. B. (2013). Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones. Journal Organic Chemistry, 78, 9464-9470. doi:10.1021/jo401191s
    • NLM

      Rosset IG, Burtoloso ACB. Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones [Internet]. Journal Organic Chemistry. 2013 ; 78 9464-9470.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo401191s
    • Vancouver

      Rosset IG, Burtoloso ACB. Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones [Internet]. Journal Organic Chemistry. 2013 ; 78 9464-9470.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo401191s
  • Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      BERNARDIM, Barbara e PINHO, Vagner D e BURTOLOSO, Antonio Carlos Bender. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D. Journal Organic Chemistry, v. 77, n. 21, p. 9926-9931, 2012Tradução . . Disponível em: https://doi.org/10.1021/jo301967w. Acesso em: 02 maio 2024.
    • APA

      Bernardim, B., Pinho, V. D., & Burtoloso, A. C. B. (2012). Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D. Journal Organic Chemistry, 77( 21), 9926-9931. doi:10.1021/jo301967w
    • NLM

      Bernardim B, Pinho VD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D [Internet]. Journal Organic Chemistry. 2012 ; 77( 21): 9926-9931.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo301967w
    • Vancouver

      Bernardim B, Pinho VD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D [Internet]. Journal Organic Chemistry. 2012 ; 77( 21): 9926-9931.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo301967w
  • Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      PINHO, Vagner D e BURTOLOSO, Antonio Carlos Bender. Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents. Journal Organic Chemistry, v. 76, n. 5, p. 289-292, 2011Tradução . . Disponível em: https://doi.org/10.1021/jo1021844. Acesso em: 02 maio 2024.
    • APA

      Pinho, V. D., & Burtoloso, A. C. B. (2011). Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents. Journal Organic Chemistry, 76( 5), 289-292. doi:10.1021/jo1021844
    • NLM

      Pinho VD, Burtoloso ACB. Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents [Internet]. Journal Organic Chemistry. 2011 ; 76( 5): 289-292.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo1021844
    • Vancouver

      Pinho VD, Burtoloso ACB. Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents [Internet]. Journal Organic Chemistry. 2011 ; 76( 5): 289-292.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo1021844
  • Source: Journal Organic Chemistry. Unidades: IFSC, IQSC

    Assunto: LEISHMANIA

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    • ABNT

      GRAY, Christopher A et al. Sulfated Meroterpenoids from the brazilian sponge callyspongia sp. are inhibitors of the antileishmaniasis target adenosine phosphoribosyl transferase. Journal Organic Chemistry, v. 71, n. 23, p. 8685-8690, 2006Tradução . . Disponível em: https://doi.org/10.1021/jo060295k. Acesso em: 02 maio 2024.
    • APA

      Gray, C. A., Lira, S. P. de, Silva, M., Pimenta, E. F., Thiemann, O. H., Oliva, G., et al. (2006). Sulfated Meroterpenoids from the brazilian sponge callyspongia sp. are inhibitors of the antileishmaniasis target adenosine phosphoribosyl transferase. Journal Organic Chemistry, 71( 23), 8685-8690. doi:10.1021/jo060295k
    • NLM

      Gray CA, Lira SP de, Silva M, Pimenta EF, Thiemann OH, Oliva G, Hajdu E, Andersen RJ, Berlinck RG de S. Sulfated Meroterpenoids from the brazilian sponge callyspongia sp. are inhibitors of the antileishmaniasis target adenosine phosphoribosyl transferase [Internet]. Journal Organic Chemistry. 2006 ; 71( 23): 8685-8690.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo060295k
    • Vancouver

      Gray CA, Lira SP de, Silva M, Pimenta EF, Thiemann OH, Oliva G, Hajdu E, Andersen RJ, Berlinck RG de S. Sulfated Meroterpenoids from the brazilian sponge callyspongia sp. are inhibitors of the antileishmaniasis target adenosine phosphoribosyl transferase [Internet]. Journal Organic Chemistry. 2006 ; 71( 23): 8685-8690.[citado 2024 maio 02 ] Available from: https://doi.org/10.1021/jo060295k

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