ReP USP - Resultado da busca

Trabalho de evento-resumo
On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors (2017)
Cianni, Lorenzo; Sartori, Geraldo; Vita, Daniela de; Rosini, Fabiana; Leitão, Andrei ; Montanari, Carlos Alberto
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: HALOGÊNIOS
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ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
Trabalho de evento-resumo
Isolation and structure of secondary metabolites from the Basidiomycete Auricularia sp (2017)
Slivinski, Juliano; Santos, Mario F. C; Gubiani, Juliana R; Berlinck, Roberto Gomes de Souza
Fonte: Proceedings. Nome do evento: IUPAC general assembly. Unidade: IQSC
Assuntos: PRODUTOS NATURAIS, FUNGICIDAS
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ABNT
SLIVINSKI, Juliano et al. Isolation and structure of secondary metabolites from the Basidiomycete Auricularia sp. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/4c23d0ac-0b95-40b8-a267-e862e2dbb76f/P16986.pdf. Acesso em: 15 jul. 2024.
APA
Slivinski, J., Santos, M. F. C., Gubiani, J. R., & Berlinck, R. G. de S. (2017). Isolation and structure of secondary metabolites from the Basidiomycete Auricularia sp. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/4c23d0ac-0b95-40b8-a267-e862e2dbb76f/P16986.pdf
NLM
Slivinski J, Santos MFC, Gubiani JR, Berlinck RG de S. Isolation and structure of secondary metabolites from the Basidiomycete Auricularia sp [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/4c23d0ac-0b95-40b8-a267-e862e2dbb76f/P16986.pdf
Vancouver
Slivinski J, Santos MFC, Gubiani JR, Berlinck RG de S. Isolation and structure of secondary metabolites from the Basidiomycete Auricularia sp [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/4c23d0ac-0b95-40b8-a267-e862e2dbb76f/P16986.pdf
Trabalho de evento-resumo
Unprecedented phomactins from the marine-derived Fungus Biatriospora sp.CBMAI 1333 (2017)
Nicacio, Karen J; Gubiani, Juliana R; Ferreira, Antonio G; Sette, Lara D; Berlinck, Roberto Gomes de Souza
Fonte: Proceedings. Nome do evento: 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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/4109e644-205c-4a77-bfce-21fde59ca06a/P16994.pdf
Trabalho de evento-resumo
Photo assusted electrochemical degradation of Tetracycline hydrochlorite (TeC) artificial urine medium (2017)
Hussain, Sajjad; Gul, Saima; Miwa, Douglas Waychi; Motheo, Artur de Jesus
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: ELETROQUÍMICA
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ABNT
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: 15 jul. 2024.
APA
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/239f9ee5-c278-4495-a1b9-254e5ea6818c/P16958.pdf
Trabalho de evento-resumo
Towards the total synthesis of the tetracyclic core of ergot alkaloids (2017)
Garambel-Vilca, Edson; Furniel, Lucas Giani; Ahmad, Anees; Burtoloso, Antonio Carlos Bender
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/88b8a76d-4c95-45b4-bc0e-f77a4af10446/P16979.pdf
Trabalho de evento-resumo
Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions (2017)
Bernardim, Barbara; Burtoloso, Antonio Carlos Bender
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
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: 15 jul. 2024.
APA
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
NLM
Bernardim B, Burtoloso ACB. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
Trabalho de evento-resumo
The effect of heat treatment on electrocatalytic performance of Cu bulk at CO2 reduction: evidence of the role of Cu2O (2017)
Lopes, Osmando F; Varela, Hamilton
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assuntos: 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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/58412c69-7338-43d9-b990-e2a46cfdcb0d/P16963.pdf
Trabalho de evento-resumo
Enhanced stability and durability of Pt and PtRu catalysts supported on functionalized graphene for HOR anodes in fuel cells (2017)
Martin, Emilio Gonzalez Hernandes; Perez, Joelma
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: CÉLULAS Á COMBUSTÍVEL
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ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/beda437f-4214-48a5-8d19-990b967b66f3/P17005.pdf
Trabalho de evento-resumo
Hydrothermal prepared IrO2 nanocatalyst for the oxygen evolution reaction: influence of the calcination temperature on the oxide proprieties and catalytic performance (2017)
Silva, Gabriel Christiano da; Perini, Nickson; Ticianelli, Edson Antonio
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: ELETROCATÁLISE
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ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/e560971c-44b9-4709-b28b-aca460991b5d/P16975.pdf
Trabalho de evento-resumo
Dimethylsiloxane-based cyclocarbonates from CO2 chemical fixation (2017)
Holanda, Carlos Alexandre; Rodrigues Filho, Ubirajara Pereira ; Imasato, Hidetake
Fonte: Proceedings. Nome do evento: IUPAC General Assemby. Unidade: IQSC
Assunto: DIÓXIDO DE CARBONO
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ABNT
HOLANDA, Carlos Alexandre e RODRIGUES FILHO, Ubirajara Pereira e IMASATO, Hidetake. Dimethylsiloxane-based cyclocarbonates from CO2 chemical fixation. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/26a93f61-7165-4d93-9226-383afabbcf3b/P16961.pdf. Acesso em: 15 jul. 2024.
APA
Holanda, C. A., Rodrigues Filho, U. P., & Imasato, H. (2017). Dimethylsiloxane-based cyclocarbonates from CO2 chemical fixation. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/26a93f61-7165-4d93-9226-383afabbcf3b/P16961.pdf
NLM
Holanda CA, Rodrigues Filho UP, Imasato H. Dimethylsiloxane-based cyclocarbonates from CO2 chemical fixation [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/26a93f61-7165-4d93-9226-383afabbcf3b/P16961.pdf
Vancouver
Holanda CA, Rodrigues Filho UP, Imasato H. Dimethylsiloxane-based cyclocarbonates from CO2 chemical fixation [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/26a93f61-7165-4d93-9226-383afabbcf3b/P16961.pdf
Trabalho de evento-resumo
On the applicability of the rotating ring-disc electrode in oxygen reduction studies: a revised vision (2017)
Gomez Marin, Ana Maria; Ticianelli, Edson Antonio
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assuntos: ELETRODO, OXIGÊNIO
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ABNT
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: 15 jul. 2024.
APA
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/97f2357b-d59e-44b9-893a-c158dfbf7d43/P16974.pdf
Trabalho de evento-resumo
Synthesis, characterization and evaluation of the antitumor activity of the cyclopalladated complexes of the type [Pd(bzan)9X)(dppp)], X=SCN, NCO (2017)
Stevanato, Alessandra; Mauro, A E; Santana, A. M; Carlos, I. Z; Santos, Regina Helena de Almeida
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: TUMOR CARCINOIDE
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ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/7b413a71-f750-452b-85ba-f7dbf425db85/P16985.pdf
Trabalho de evento-resumo
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)
Gonçalves, Andressa Dancini; Buoro, Rafael Martos
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assuntos: VOLTAMETRIA, ACIDO ÚRICO
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ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/aebadad2-ba19-4069-b907-86b8e9fa45fa/P16983.pdf
Trabalho de evento-resumo
Synthesis of gold nanoparticles: the role of glycerol as reducing-cum-stabilizing agent (2017)
Tremiliosi Filho, Germano ; Ullah, Sajjad; Parven, Rashida
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: NANOPARTÍCULAS
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ABNT
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: 15 jul. 2024.
APA
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/dc64e0a7-8f41-4e79-ad50-4411c0d10a72/P16965.pdf
Trabalho de evento-resumo
Synthesis and characterization of the fac-[Re(CO)3(Bz-N(CH2)2N-Bz)]Br as standard for fac-[99mTc(CO)3(Bz-N(CH2)2N(CH2)2N-Bz]+, a potential tumor imaging agent (2017)
Marques, F L N; Chaves, H K; Lafratta, A. E; Deflon, Victor Marcelo
Fonte: Proceedings. Nome do evento: IUPAC General Chemistry. Unidade: IQSC
Assunto: MEDICINA NUCLEAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARQUES, F L N et al. Synthesis and characterization of the fac-[Re(CO)3(Bz-N(CH2)2N-Bz)]Br as standard for fac-[99mTc(CO)3(Bz-N(CH2)2N(CH2)2N-Bz]+, a potential tumor imaging agent. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/069929c9-f873-4688-a4db-59094de242cf/P16991.pdf. Acesso em: 15 jul. 2024.
APA
Marques, F. L. N., Chaves, H. K., Lafratta, A. E., & Deflon, V. M. (2017). Synthesis and characterization of the fac-[Re(CO)3(Bz-N(CH2)2N-Bz)]Br as standard for fac-[99mTc(CO)3(Bz-N(CH2)2N(CH2)2N-Bz]+, a potential tumor imaging agent. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/069929c9-f873-4688-a4db-59094de242cf/P16991.pdf
NLM
Marques FLN, Chaves HK, Lafratta AE, Deflon VM. Synthesis and characterization of the fac-[Re(CO)3(Bz-N(CH2)2N-Bz)]Br as standard for fac-[99mTc(CO)3(Bz-N(CH2)2N(CH2)2N-Bz]+, a potential tumor imaging agent [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/069929c9-f873-4688-a4db-59094de242cf/P16991.pdf
Vancouver
Marques FLN, Chaves HK, Lafratta AE, Deflon VM. Synthesis and characterization of the fac-[Re(CO)3(Bz-N(CH2)2N-Bz)]Br as standard for fac-[99mTc(CO)3(Bz-N(CH2)2N(CH2)2N-Bz]+, a potential tumor imaging agent [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/069929c9-f873-4688-a4db-59094de242cf/P16991.pdf
Trabalho de evento-resumo
Synthesis of bicyclic nitrogen heterocycles via cascade reaction from N-terminal alfa,gama-unsaturated diazoketones (2017)
Silva, João Victor Santiago da; Burtoloso, Antonio Carlos Bender
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 15 jul. 2024.
APA
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/
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
The electrochemical oxidation mechanism of dipyrone and the antipyrines: the construction of a puzzle (2017)
Bacil, Raphael P; Buoro, Rafael Martos ; Campos, Othon Souto; Ramos, Matesa A; Gomes, Caroline S; Serrano, Silvia Helena Pires
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidades: IQ, IQSC
Assuntos: ANALGÉSICOS, ELETROQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/a1024c9d-42b7-4bc2-b345-10b100af8f62/P16997.pdf
Vancouver
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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/a1024c9d-42b7-4bc2-b345-10b100af8f62/P16997.pdf
Trabalho de evento-resumo
Rheological behavior of chitosan/gelatin/pracaxi oil emulsions (2017)
Horn, Marilia Marta; Rodrigues, Murilo Álison Vigilato; Martins, Virginia da Conceição Amaro; Plepis, Ana Maria de Guzzi
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assuntos: REOLOGIA, QUITOSANA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HORN, Marilia Marta et al. Rheological behavior of chitosan/gelatin/pracaxi oil emulsions. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 15 jul. 2024.
APA
Horn, M. M., Rodrigues, M. Á. V., Martins, V. da C. A., & Plepis, A. M. de G. (2017). Rheological behavior of chitosan/gelatin/pracaxi oil emulsions. In Proceedings. Durham: IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Horn MM, Rodrigues MÁV, Martins V da CA, Plepis AM de G. Rheological behavior of chitosan/gelatin/pracaxi oil emulsions [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Horn MM, Rodrigues MÁV, Martins V da CA, Plepis AM de G. Rheological behavior of chitosan/gelatin/pracaxi oil emulsions [Internet]. Proceedings. 2017 ;[citado 2024 jul. 15 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
An epoxide ring-opening strategy for short and steroselective synthesis of brussonol analogues (2017)
Ahmad, Anees; Burtoloso, Antonio Carlos Bender
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 15 jul. 2024.
APA
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 jul. 15 ] 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 jul. 15 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Molecular networking as a dereplication tool to prioritize natural product diversity in a collection of endophytic fungi strains based on extraction protocols (2017)
Urano, Raquel Peres de Morais; Gubiani, Juliana R; Venâncio, Victor Alves; Tomazela, Daniela; Felício, Rafael de; Ferreira, Everton L. F; Trivella, Daniela B. B; Lira, Simone P; Berlinck, Roberto Gomes de Souza
Fonte: Proceedings. Nome do evento: IUPAC General Assembly. Unidade: IQSC
Assuntos: PRODUTOS NATURAIS, FUNGICIDAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 15 jul. 2024.
APA
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
NLM
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 jul. 15 ] 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 jul. 15 ] Available from: https://repositorio.usp.br/directbitstream/3426468f-204b-4c3d-a4dc-ee893604db54/P17001.pdf

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