Filtros : "Proceedings" "IUPAC General Assembly" Removidos: "ENSINO / B3" "França" "Polônia" "Ramires, José Antônio Franchini" Limpar

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  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: BIOLOGIA MARINHA

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      NICACIO, Karen J et al. Unprecedented phomactins from the marine-derived Fungus Biatriospora sp.CBMAI 1333. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/4109e644-205c-4a77-bfce-21fde59ca06a/P16994.pdf. Acesso em: 05 nov. 2024.
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      Nicacio, K. J., Gubiani, J. R., Ferreira, A. G., Sette, L. D., & Berlinck, R. G. de S. (2017). Unprecedented phomactins from the marine-derived Fungus Biatriospora sp.CBMAI 1333. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/4109e644-205c-4a77-bfce-21fde59ca06a/P16994.pdf
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      Nicacio KJ, Gubiani JR, Ferreira AG, Sette LD, Berlinck RG de S. Unprecedented phomactins from the marine-derived Fungus Biatriospora sp.CBMAI 1333 [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/4109e644-205c-4a77-bfce-21fde59ca06a/P16994.pdf
    • Vancouver

      Nicacio KJ, Gubiani JR, Ferreira AG, Sette LD, Berlinck RG de S. Unprecedented phomactins from the marine-derived Fungus Biatriospora sp.CBMAI 1333 [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/4109e644-205c-4a77-bfce-21fde59ca06a/P16994.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidades: EACH, IQSC

    Assunto: ALCALÓIDES

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      FREIRE, Vitor F e COLOMBO, Renata e YARIWAKE, Janete Harumi. Analysis of beta-carboline alkaloids in Passiflora edulis peels. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/9560a608-276e-49b4-a22c-fcac72c99f19/P16956.pdf. Acesso em: 05 nov. 2024.
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      Freire, V. F., Colombo, R., & Yariwake, J. H. (2017). Analysis of beta-carboline alkaloids in Passiflora edulis peels. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/9560a608-276e-49b4-a22c-fcac72c99f19/P16956.pdf
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      Freire VF, Colombo R, Yariwake JH. Analysis of beta-carboline alkaloids in Passiflora edulis peels [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/9560a608-276e-49b4-a22c-fcac72c99f19/P16956.pdf
    • Vancouver

      Freire VF, Colombo R, Yariwake JH. Analysis of beta-carboline alkaloids in Passiflora edulis peels [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/9560a608-276e-49b4-a22c-fcac72c99f19/P16956.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: HALOGÊNIOS

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      CIANNI, Lorenzo et al. On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf. Acesso em: 05 nov. 2024.
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      Cianni, L., Sartori, G., Vita, D. de, Rosini, F., Leitão, A., & Montanari, C. A. (2017). On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
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      Cianni L, Sartori G, Vita D de, Rosini F, Leitão A, Montanari CA. On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
    • Vancouver

      Cianni L, Sartori G, Vita D de, Rosini F, Leitão A, Montanari CA. On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      GARAMBEL-VILCA, Edson et al. Towards the total synthesis of the tetracyclic core of ergot alkaloids. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/88b8a76d-4c95-45b4-bc0e-f77a4af10446/P16979.pdf. Acesso em: 05 nov. 2024.
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      Garambel-Vilca, E., Furniel, L. G., Ahmad, A., & Burtoloso, A. C. B. (2017). Towards the total synthesis of the tetracyclic core of ergot alkaloids. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/88b8a76d-4c95-45b4-bc0e-f77a4af10446/P16979.pdf
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      Garambel-Vilca E, Furniel LG, Ahmad A, Burtoloso ACB. Towards the total synthesis of the tetracyclic core of ergot alkaloids [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/88b8a76d-4c95-45b4-bc0e-f77a4af10446/P16979.pdf
    • Vancouver

      Garambel-Vilca E, Furniel LG, Ahmad A, Burtoloso ACB. Towards the total synthesis of the tetracyclic core of ergot alkaloids [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/88b8a76d-4c95-45b4-bc0e-f77a4af10446/P16979.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf. Acesso em: 05 nov. 2024.
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      Bernardim, B., & Burtoloso, A. C. B. (2017). Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
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      Bernardim B, Burtoloso ACB. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
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      Bernardim B, Burtoloso ACB. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: ELETROQUÍMICA

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      HUSSAIN, Sajjad et al. Photo assusted electrochemical degradation of Tetracycline hydrochlorite (TeC) artificial urine medium. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/239f9ee5-c278-4495-a1b9-254e5ea6818c/P16958.pdf. Acesso em: 05 nov. 2024.
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      Hussain, S., Gul, S., Miwa, D. W., & Motheo, A. de J. (2017). Photo assusted electrochemical degradation of Tetracycline hydrochlorite (TeC) artificial urine medium. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/239f9ee5-c278-4495-a1b9-254e5ea6818c/P16958.pdf
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      Hussain S, Gul S, Miwa DW, Motheo A de J. Photo assusted electrochemical degradation of Tetracycline hydrochlorite (TeC) artificial urine medium [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/239f9ee5-c278-4495-a1b9-254e5ea6818c/P16958.pdf
    • Vancouver

      Hussain S, Gul S, Miwa DW, Motheo A de J. Photo assusted electrochemical degradation of Tetracycline hydrochlorite (TeC) artificial urine medium [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/239f9ee5-c278-4495-a1b9-254e5ea6818c/P16958.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: TRATAMENTO TÉRMICO, ELETROCATÁLISE

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      LOPES, Osmando F e VARELA, Hamilton. The effect of heat treatment on electrocatalytic performance of Cu bulk at CO2 reduction: evidence of the role of Cu2O. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/58412c69-7338-43d9-b990-e2a46cfdcb0d/P16963.pdf. Acesso em: 05 nov. 2024.
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      Lopes, O. F., & Varela, H. (2017). The effect of heat treatment on electrocatalytic performance of Cu bulk at CO2 reduction: evidence of the role of Cu2O. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/58412c69-7338-43d9-b990-e2a46cfdcb0d/P16963.pdf
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      Lopes OF, Varela H. The effect of heat treatment on electrocatalytic performance of Cu bulk at CO2 reduction: evidence of the role of Cu2O [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/58412c69-7338-43d9-b990-e2a46cfdcb0d/P16963.pdf
    • Vancouver

      Lopes OF, Varela H. The effect of heat treatment on electrocatalytic performance of Cu bulk at CO2 reduction: evidence of the role of Cu2O [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/58412c69-7338-43d9-b990-e2a46cfdcb0d/P16963.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: ELETRODO, OXIGÊNIO

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      GOMEZ MARIN, Ana Maria e TICIANELLI, Edson Antonio. On the applicability of the rotating ring-disc electrode in oxygen reduction studies: a revised vision. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/97f2357b-d59e-44b9-893a-c158dfbf7d43/P16974.pdf. Acesso em: 05 nov. 2024.
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      Gomez Marin, A. M., & Ticianelli, E. A. (2017). On the applicability of the rotating ring-disc electrode in oxygen reduction studies: a revised vision. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/97f2357b-d59e-44b9-893a-c158dfbf7d43/P16974.pdf
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      Gomez Marin AM, Ticianelli EA. On the applicability of the rotating ring-disc electrode in oxygen reduction studies: a revised vision [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/97f2357b-d59e-44b9-893a-c158dfbf7d43/P16974.pdf
    • Vancouver

      Gomez Marin AM, Ticianelli EA. On the applicability of the rotating ring-disc electrode in oxygen reduction studies: a revised vision [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/97f2357b-d59e-44b9-893a-c158dfbf7d43/P16974.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: ELETROCATÁLISE

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      SILVA, Gabriel Christiano da e PERINI, Nickson e TICIANELLI, Edson Antonio. Hydrothermal prepared IrO2 nanocatalyst for the oxygen evolution reaction: influence of the calcination temperature on the oxide proprieties and catalytic performance. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/e560971c-44b9-4709-b28b-aca460991b5d/P16975.pdf. Acesso em: 05 nov. 2024.
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      Silva, G. C. da, Perini, N., & Ticianelli, E. A. (2017). Hydrothermal prepared IrO2 nanocatalyst for the oxygen evolution reaction: influence of the calcination temperature on the oxide proprieties and catalytic performance. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/e560971c-44b9-4709-b28b-aca460991b5d/P16975.pdf
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      Silva GC da, Perini N, Ticianelli EA. Hydrothermal prepared IrO2 nanocatalyst for the oxygen evolution reaction: influence of the calcination temperature on the oxide proprieties and catalytic performance [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/e560971c-44b9-4709-b28b-aca460991b5d/P16975.pdf
    • Vancouver

      Silva GC da, Perini N, Ticianelli EA. Hydrothermal prepared IrO2 nanocatalyst for the oxygen evolution reaction: influence of the calcination temperature on the oxide proprieties and catalytic performance [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/e560971c-44b9-4709-b28b-aca460991b5d/P16975.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: CÉLULAS Á COMBUSTÍVEL

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      MARTIN, Emilio Gonzalez Hernandes e PEREZ, Joelma. Enhanced stability and durability of Pt and PtRu catalysts supported on functionalized graphene for HOR anodes in fuel cells. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/beda437f-4214-48a5-8d19-990b967b66f3/P17005.pdf. Acesso em: 05 nov. 2024.
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      Martin, E. G. H., & Perez, J. (2017). Enhanced stability and durability of Pt and PtRu catalysts supported on functionalized graphene for HOR anodes in fuel cells. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/beda437f-4214-48a5-8d19-990b967b66f3/P17005.pdf
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      Martin EGH, Perez J. Enhanced stability and durability of Pt and PtRu catalysts supported on functionalized graphene for HOR anodes in fuel cells [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/beda437f-4214-48a5-8d19-990b967b66f3/P17005.pdf
    • Vancouver

      Martin EGH, Perez J. Enhanced stability and durability of Pt and PtRu catalysts supported on functionalized graphene for HOR anodes in fuel cells [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/beda437f-4214-48a5-8d19-990b967b66f3/P17005.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: NANOPARTÍCULAS

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      TREMILIOSI FILHO, Germano e ULLAH, Sajjad e PARVEN, Rashida. Synthesis of gold nanoparticles: the role of glycerol as reducing-cum-stabilizing agent. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/dc64e0a7-8f41-4e79-ad50-4411c0d10a72/P16965.pdf. Acesso em: 05 nov. 2024.
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      Tremiliosi Filho, G., Ullah, S., & Parven, R. (2017). Synthesis of gold nanoparticles: the role of glycerol as reducing-cum-stabilizing agent. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/dc64e0a7-8f41-4e79-ad50-4411c0d10a72/P16965.pdf
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      Tremiliosi Filho G, Ullah S, Parven R. Synthesis of gold nanoparticles: the role of glycerol as reducing-cum-stabilizing agent [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/dc64e0a7-8f41-4e79-ad50-4411c0d10a72/P16965.pdf
    • Vancouver

      Tremiliosi Filho G, Ullah S, Parven R. Synthesis of gold nanoparticles: the role of glycerol as reducing-cum-stabilizing agent [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/dc64e0a7-8f41-4e79-ad50-4411c0d10a72/P16965.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      SILVA, João Victor Santiago da e BURTOLOSO, Antonio Carlos Bender. Synthesis of bicyclic nitrogen heterocycles via cascade reaction from N-terminal alfa,gama-unsaturated diazoketones. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 05 nov. 2024.
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      Silva, J. V. S. da, & Burtoloso, A. C. B. (2017). Synthesis of bicyclic nitrogen heterocycles via cascade reaction from N-terminal alfa,gama-unsaturated diazoketones. In Proceedings. Durham: IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
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      Silva JVS da, Burtoloso ACB. Synthesis of bicyclic nitrogen heterocycles via cascade reaction from N-terminal alfa,gama-unsaturated diazoketones [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
    • Vancouver

      Silva JVS da, Burtoloso ACB. Synthesis of bicyclic nitrogen heterocycles via cascade reaction from N-terminal alfa,gama-unsaturated diazoketones [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: TUMOR CARCINOIDE

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      STEVANATO, Alessandra et al. Synthesis, characterization and evaluation of the antitumor activity of the cyclopalladated complexes of the type [Pd(bzan)9X)(dppp)], X=SCN, NCO. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/7b413a71-f750-452b-85ba-f7dbf425db85/P16985.pdf. Acesso em: 05 nov. 2024.
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      Stevanato, A., Mauro, A. E., Santana, A. M., Carlos, I. Z., & Santos, R. H. de A. (2017). Synthesis, characterization and evaluation of the antitumor activity of the cyclopalladated complexes of the type [Pd(bzan)9X)(dppp)], X=SCN, NCO. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/7b413a71-f750-452b-85ba-f7dbf425db85/P16985.pdf
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      Stevanato A, Mauro AE, Santana AM, Carlos IZ, Santos RH de A. Synthesis, characterization and evaluation of the antitumor activity of the cyclopalladated complexes of the type [Pd(bzan)9X)(dppp)], X=SCN, NCO [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/7b413a71-f750-452b-85ba-f7dbf425db85/P16985.pdf
    • Vancouver

      Stevanato A, Mauro AE, Santana AM, Carlos IZ, Santos RH de A. Synthesis, characterization and evaluation of the antitumor activity of the cyclopalladated complexes of the type [Pd(bzan)9X)(dppp)], X=SCN, NCO [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/7b413a71-f750-452b-85ba-f7dbf425db85/P16985.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: VOLTAMETRIA, ACIDO ÚRICO

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      GONÇALVES, Andressa Dancini e BUORO, Rafael Martos. Voltammetric sensing of Tryptophan and uric acid in the presence of ascorbic acid at a pre-activated nickel-oxide nanoestructured modified glassy carbon electrode. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/aebadad2-ba19-4069-b907-86b8e9fa45fa/P16983.pdf. Acesso em: 05 nov. 2024.
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      Gonçalves, A. D., & Buoro, R. M. (2017). Voltammetric sensing of Tryptophan and uric acid in the presence of ascorbic acid at a pre-activated nickel-oxide nanoestructured modified glassy carbon electrode. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/aebadad2-ba19-4069-b907-86b8e9fa45fa/P16983.pdf
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      Gonçalves AD, Buoro RM. Voltammetric sensing of Tryptophan and uric acid in the presence of ascorbic acid at a pre-activated nickel-oxide nanoestructured modified glassy carbon electrode [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/aebadad2-ba19-4069-b907-86b8e9fa45fa/P16983.pdf
    • Vancouver

      Gonçalves AD, Buoro RM. Voltammetric sensing of Tryptophan and uric acid in the presence of ascorbic acid at a pre-activated nickel-oxide nanoestructured modified glassy carbon electrode [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/aebadad2-ba19-4069-b907-86b8e9fa45fa/P16983.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: PRODUTOS NATURAIS, FUNGICIDAS

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      URANO, Raquel Peres de Morais et al. Molecular networking as a dereplication tool to prioritize natural product diversity in a collection of endophytic fungi strains based on extraction protocols. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/3426468f-204b-4c3d-a4dc-ee893604db54/P17001.pdf. Acesso em: 05 nov. 2024.
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      Urano, R. P. de M., Gubiani, J. R., Venâncio, V. A., Tomazela, D., Felício, R. de, Ferreira, E. L. F., et al. (2017). Molecular networking as a dereplication tool to prioritize natural product diversity in a collection of endophytic fungi strains based on extraction protocols. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/3426468f-204b-4c3d-a4dc-ee893604db54/P17001.pdf
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      Urano RP de M, Gubiani JR, Venâncio VA, Tomazela D, Felício R de, Ferreira ELF, Trivella DBB, Lira SP, Berlinck RG de S. Molecular networking as a dereplication tool to prioritize natural product diversity in a collection of endophytic fungi strains based on extraction protocols [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/3426468f-204b-4c3d-a4dc-ee893604db54/P17001.pdf
    • Vancouver

      Urano RP de M, Gubiani JR, Venâncio VA, Tomazela D, Felício R de, Ferreira ELF, Trivella DBB, Lira SP, Berlinck RG de S. Molecular networking as a dereplication tool to prioritize natural product diversity in a collection of endophytic fungi strains based on extraction protocols [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/3426468f-204b-4c3d-a4dc-ee893604db54/P17001.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: BIOLOGIA MARINHA, PARASITOLOGIA

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      BERTONHA, Ariane Fernandes et al. Synthesis and structure-activity relationship studies of antiparasitic Pseudoceratidine derivatives. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/ff1a3161-f7af-4a78-a1e9-726529963f4a/P16993.pdf. Acesso em: 05 nov. 2024.
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      Bertonha, A. F., Parra, L. L. L., Tempone, A. G., Miguel, D. C., Romo, D., & Berlinck, R. G. de S. (2017). Synthesis and structure-activity relationship studies of antiparasitic Pseudoceratidine derivatives. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/ff1a3161-f7af-4a78-a1e9-726529963f4a/P16993.pdf
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      Bertonha AF, Parra LLL, Tempone AG, Miguel DC, Romo D, Berlinck RG de S. Synthesis and structure-activity relationship studies of antiparasitic Pseudoceratidine derivatives [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/ff1a3161-f7af-4a78-a1e9-726529963f4a/P16993.pdf
    • Vancouver

      Bertonha AF, Parra LLL, Tempone AG, Miguel DC, Romo D, Berlinck RG de S. Synthesis and structure-activity relationship studies of antiparasitic Pseudoceratidine derivatives [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/ff1a3161-f7af-4a78-a1e9-726529963f4a/P16993.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: PROTEÍNAS, ESPECTROSCOPIA DE MASSA

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      BATISTON, Weliton Pedro e SANTOS NETO, Alvaro Jose dos e CARRILHO, Emanuel. Increasing coverage in shotgun proteomics in the SCXxRP-MS/MS method. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/4f1fe388-da69-4e2b-aa7b-39614a62b784/P16970.pdf. Acesso em: 05 nov. 2024.
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      Batiston, W. P., Santos Neto, A. J. dos, & Carrilho, E. (2017). Increasing coverage in shotgun proteomics in the SCXxRP-MS/MS method. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/4f1fe388-da69-4e2b-aa7b-39614a62b784/P16970.pdf
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      Batiston WP, Santos Neto AJ dos, Carrilho E. Increasing coverage in shotgun proteomics in the SCXxRP-MS/MS method [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/4f1fe388-da69-4e2b-aa7b-39614a62b784/P16970.pdf
    • Vancouver

      Batiston WP, Santos Neto AJ dos, Carrilho E. Increasing coverage in shotgun proteomics in the SCXxRP-MS/MS method [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/4f1fe388-da69-4e2b-aa7b-39614a62b784/P16970.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidades: EACH, IQSC

    Assunto: QUÍMICA AMBIENTAL

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      COLOMBO, Renata e YARIWAKE, Janete Harumi e LANZA, Marcos Roberto de Vasconcelos. Evaluation of the lambda-cyhalothrin behavior in aqueous media by using chemical oxidative process. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/51634126-fbea-4621-b3ed-b2072d0f0127/P16955.pdf. Acesso em: 05 nov. 2024.
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      Colombo, R., Yariwake, J. H., & Lanza, M. R. de V. (2017). Evaluation of the lambda-cyhalothrin behavior in aqueous media by using chemical oxidative process. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/51634126-fbea-4621-b3ed-b2072d0f0127/P16955.pdf
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      Colombo R, Yariwake JH, Lanza MR de V. Evaluation of the lambda-cyhalothrin behavior in aqueous media by using chemical oxidative process [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/51634126-fbea-4621-b3ed-b2072d0f0127/P16955.pdf
    • Vancouver

      Colombo R, Yariwake JH, Lanza MR de V. Evaluation of the lambda-cyhalothrin behavior in aqueous media by using chemical oxidative process [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/51634126-fbea-4621-b3ed-b2072d0f0127/P16955.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidades: IQ, IQSC

    Subjects: ANALGÉSICOS, ELETROQUÍMICA

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      BACIL, Raphael P et al. The electrochemical oxidation mechanism of dipyrone and the antipyrines: the construction of a puzzle. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/a1024c9d-42b7-4bc2-b345-10b100af8f62/P16997.pdf. Acesso em: 05 nov. 2024.
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      Bacil, R. P., Buoro, R. M., Campos, O. S., Ramos, M. A., Gomes, C. S., & Serrano, S. H. P. (2017). The electrochemical oxidation mechanism of dipyrone and the antipyrines: the construction of a puzzle. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/a1024c9d-42b7-4bc2-b345-10b100af8f62/P16997.pdf
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      Bacil RP, Buoro RM, Campos OS, Ramos MA, Gomes CS, Serrano SHP. The electrochemical oxidation mechanism of dipyrone and the antipyrines: the construction of a puzzle [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/a1024c9d-42b7-4bc2-b345-10b100af8f62/P16997.pdf
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      Bacil RP, Buoro RM, Campos OS, Ramos MA, Gomes CS, Serrano SHP. The electrochemical oxidation mechanism of dipyrone and the antipyrines: the construction of a puzzle [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/a1024c9d-42b7-4bc2-b345-10b100af8f62/P16997.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: PRODUTOS NATURAIS

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      BERLINCK, Roberto Gomes de Souza et al. Drug discovery from marine natural products in Brazil. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/992bf250-eea1-4e79-8095-dae3866b1af5/P16998.pdf. Acesso em: 05 nov. 2024.
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      Berlinck, R. G. de S., Nicacio, K. J., Ióca, L. P., Ferreira, E. L. F., Bertonha, A. F., Rodríguez, J. P. G., et al. (2017). Drug discovery from marine natural products in Brazil. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/992bf250-eea1-4e79-8095-dae3866b1af5/P16998.pdf
    • NLM

      Berlinck RG de S, Nicacio KJ, Ióca LP, Ferreira ELF, Bertonha AF, Rodríguez JPG, Takaki M, Slivinski J, Souza RTMP, Morais-Urano RP, Gubiani JR, Tonon LAC, Tomazela D, Venâncio VA, Rabello B. Drug discovery from marine natural products in Brazil [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/992bf250-eea1-4e79-8095-dae3866b1af5/P16998.pdf
    • Vancouver

      Berlinck RG de S, Nicacio KJ, Ióca LP, Ferreira ELF, Bertonha AF, Rodríguez JPG, Takaki M, Slivinski J, Souza RTMP, Morais-Urano RP, Gubiani JR, Tonon LAC, Tomazela D, Venâncio VA, Rabello B. Drug discovery from marine natural products in Brazil [Internet]. Proceedings. 2017 ;[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/992bf250-eea1-4e79-8095-dae3866b1af5/P16998.pdf

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