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  • 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: 17 maio 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
    • Vancouver

      Bernardim B, Burtoloso ACB. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/88b8a76d-4c95-45b4-bc0e-f77a4af10446/P16979.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: 17 maio 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
    • NLM

      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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/239f9ee5-c278-4495-a1b9-254e5ea6818c/P16958.pdf
  • 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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/4109e644-205c-4a77-bfce-21fde59ca06a/P16994.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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/58412c69-7338-43d9-b990-e2a46cfdcb0d/P16963.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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/beda437f-4214-48a5-8d19-990b967b66f3/P17005.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: 17 maio 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
    • NLM

      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 maio 17 ] 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 maio 17 ] 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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/e560971c-44b9-4709-b28b-aca460991b5d/P16975.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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
  • 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: 17 maio 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
    • NLM

      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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/dc64e0a7-8f41-4e79-ad50-4411c0d10a72/P16965.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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/ff1a3161-f7af-4a78-a1e9-726529963f4a/P16993.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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/3426468f-204b-4c3d-a4dc-ee893604db54/P17001.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      AHMAD, Anees e BURTOLOSO, Antonio Carlos Bender. An epoxide ring-opening strategy for short and steroselective synthesis of brussonol analogues. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 17 maio 2024.
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      Ahmad, A., & Burtoloso, A. C. B. (2017). An epoxide ring-opening strategy for short and steroselective synthesis of brussonol analogues. In Proceedings. Durham: IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
    • NLM

      Ahmad A, Burtoloso ACB. An epoxide ring-opening strategy for short and steroselective synthesis of brussonol analogues [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
    • Vancouver

      Ahmad A, Burtoloso ACB. An epoxide ring-opening strategy for short and steroselective synthesis of brussonol analogues [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
  • 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: 17 maio 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
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      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 maio 17 ] 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 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/992bf250-eea1-4e79-8095-dae3866b1af5/P16998.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      MOMO, Patrícia Betoni e DIAS, Rafael Mafra de Paula e BURTOLOSO, Antonio Carlos Bender. One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf. Acesso em: 17 maio 2024.
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      Momo, P. B., Dias, R. M. de P., & Burtoloso, A. C. B. (2017). One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf
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      Momo PB, Dias RM de P, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf
    • Vancouver

      Momo PB, Dias RM de P, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: QUITOSANA

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      TIERA, Vera Aparecida de Oliveira et al. Amphiphilic derivatives of Diethylaminoethyl chitosan: antifungal activity against A.Flavus via fungistatic mechanism. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/e42cdd78-ea68-4922-9894-467caaa491d3/P16995.pdf. Acesso em: 17 maio 2024.
    • APA

      Tiera, V. A. de O., Dias, A. M., Gabriel, J. S., Taboga, S. R., Vilamaior, P. S. L., Leves, A. L. P., et al. (2017). Amphiphilic derivatives of Diethylaminoethyl chitosan: antifungal activity against A.Flavus via fungistatic mechanism. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/e42cdd78-ea68-4922-9894-467caaa491d3/P16995.pdf
    • NLM

      Tiera VA de O, Dias AM, Gabriel JS, Taboga SR, Vilamaior PSL, Leves ALP, Cabrera MP dos S, Cavalheiro CCS, Tiera MJ. Amphiphilic derivatives of Diethylaminoethyl chitosan: antifungal activity against A.Flavus via fungistatic mechanism [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/e42cdd78-ea68-4922-9894-467caaa491d3/P16995.pdf
    • Vancouver

      Tiera VA de O, Dias AM, Gabriel JS, Taboga SR, Vilamaior PSL, Leves ALP, Cabrera MP dos S, Cavalheiro CCS, Tiera MJ. Amphiphilic derivatives of Diethylaminoethyl chitosan: antifungal activity against A.Flavus via fungistatic mechanism [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/e42cdd78-ea68-4922-9894-467caaa491d3/P16995.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: CELULOSE, ETANOL

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      FROLLINI, Elisabete et al. Bio-based materials and cellulosic ethanol from lignocellosic fibers. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/727f2480-4721-4d11-87f0-fedd8aaaa0f6/P16996.pdf. Acesso em: 17 maio 2024.
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      Frollini, E., Cassales, A. R., Gomes, B. L., Oliveira, F. de, Kaschuk, J. J., Pinheiro, F. G. C., et al. (2017). Bio-based materials and cellulosic ethanol from lignocellosic fibers. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/727f2480-4721-4d11-87f0-fedd8aaaa0f6/P16996.pdf
    • NLM

      Frollini E, Cassales AR, Gomes BL, Oliveira F de, Kaschuk JJ, Pinheiro FGC, Catunda L, Rossi PF, Santos RP de O, Ferracini T. Bio-based materials and cellulosic ethanol from lignocellosic fibers [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/727f2480-4721-4d11-87f0-fedd8aaaa0f6/P16996.pdf
    • Vancouver

      Frollini E, Cassales AR, Gomes BL, Oliveira F de, Kaschuk JJ, Pinheiro FGC, Catunda L, Rossi PF, Santos RP de O, Ferracini T. Bio-based materials and cellulosic ethanol from lignocellosic fibers [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/727f2480-4721-4d11-87f0-fedd8aaaa0f6/P16996.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: ALCALÓIDES

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      NAGENDRA, Siddavatam et al. Asymmetric synthesis of a Batzelladine Analogues. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/bb40540c-bdbf-4d57-8759-80d9675b9831/P16988.pdf. Acesso em: 17 maio 2024.
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      Nagendra, S., Overman, L. E., Berlinck, R. G. de S., & Pilli, R. A. (2017). Asymmetric synthesis of a Batzelladine Analogues. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/bb40540c-bdbf-4d57-8759-80d9675b9831/P16988.pdf
    • NLM

      Nagendra S, Overman LE, Berlinck RG de S, Pilli RA. Asymmetric synthesis of a Batzelladine Analogues [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/bb40540c-bdbf-4d57-8759-80d9675b9831/P16988.pdf
    • Vancouver

      Nagendra S, Overman LE, Berlinck RG de S, Pilli RA. Asymmetric synthesis of a Batzelladine Analogues [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/bb40540c-bdbf-4d57-8759-80d9675b9831/P16988.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: ALCALOIDES

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      TAKAKI, Mirelle e PADULA, Vinicius e BERLINCK, Roberto Gomes de Souza. Metabolomics of the Nudibranch Roboatra ernsti. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/60bc5630-7945-4ebd-af85-18ea2f6bae80/P16987.pdf. Acesso em: 17 maio 2024.
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      Takaki, M., Padula, V., & Berlinck, R. G. de S. (2017). Metabolomics of the Nudibranch Roboatra ernsti. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/60bc5630-7945-4ebd-af85-18ea2f6bae80/P16987.pdf
    • NLM

      Takaki M, Padula V, Berlinck RG de S. Metabolomics of the Nudibranch Roboatra ernsti [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/60bc5630-7945-4ebd-af85-18ea2f6bae80/P16987.pdf
    • Vancouver

      Takaki M, Padula V, Berlinck RG de S. Metabolomics of the Nudibranch Roboatra ernsti [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/60bc5630-7945-4ebd-af85-18ea2f6bae80/P16987.pdf
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Subjects: BACTÉRIAS, BIOLOGIA MARINHA

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      NICACIO, Karen J et al. Brominated secondary metabolites produced by the marine bacterium Pseudovibrio denitrificans Ab134. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/930c05c6-ca5b-4b49-8c8d-ea13342fe9f4/P16992.pdf. Acesso em: 17 maio 2024.
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      Nicacio, K. J., Ióca, L. P., Thompson, F., Ferreira, A. G., & Berlinck, R. G. de S. (2017). Brominated secondary metabolites produced by the marine bacterium Pseudovibrio denitrificans Ab134. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/930c05c6-ca5b-4b49-8c8d-ea13342fe9f4/P16992.pdf
    • NLM

      Nicacio KJ, Ióca LP, Thompson F, Ferreira AG, Berlinck RG de S. Brominated secondary metabolites produced by the marine bacterium Pseudovibrio denitrificans Ab134 [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/930c05c6-ca5b-4b49-8c8d-ea13342fe9f4/P16992.pdf
    • Vancouver

      Nicacio KJ, Ióca LP, Thompson F, Ferreira AG, Berlinck RG de S. Brominated secondary metabolites produced by the marine bacterium Pseudovibrio denitrificans Ab134 [Internet]. Proceedings. 2017 ;[citado 2024 maio 17 ] Available from: https://repositorio.usp.br/directbitstream/930c05c6-ca5b-4b49-8c8d-ea13342fe9f4/P16992.pdf

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