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
Source: Proceedings. Conference titles: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
Trabalho de evento-resumo
One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin (2017)
Momo, Patrícia Betoni; Dias, Rafael Mafra de Paula; Burtoloso, Antonio Carlos Bender
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
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: 01 maio 2026.
APA
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
NLM
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf
Trabalho de evento-resumo
Functionalization of a cyclic olefin with fatty alcohols from babassu oil and its polimerization via ROMP (2017)
Costa, Pedro F G M da; Fernandes, Henrique; Batista, Nouga Cardoso; Lima Neto, Benedito dos Santos
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: BABAÇU
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COSTA, Pedro F G M da et al. Functionalization of a cyclic olefin with fatty alcohols from babassu oil and its polimerization via ROMP. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/1b4d609b-51ee-4766-909e-ff94924feb04/P16977.pdf. Acesso em: 01 maio 2026.
APA
Costa, P. F. G. M. da, Fernandes, H., Batista, N. C., & Lima Neto, B. dos S. (2017). Functionalization of a cyclic olefin with fatty alcohols from babassu oil and its polimerization via ROMP. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/1b4d609b-51ee-4766-909e-ff94924feb04/P16977.pdf
NLM
Costa PFGM da, Fernandes H, Batista NC, Lima Neto B dos S. Functionalization of a cyclic olefin with fatty alcohols from babassu oil and its polimerization via ROMP [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/1b4d609b-51ee-4766-909e-ff94924feb04/P16977.pdf
Vancouver
Costa PFGM da, Fernandes H, Batista NC, Lima Neto B dos S. Functionalization of a cyclic olefin with fatty alcohols from babassu oil and its polimerization via ROMP [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/1b4d609b-51ee-4766-909e-ff94924feb04/P16977.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
Source: Proceedings. Conference titles: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] 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
Source: Proceedings. Conference titles: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
Trabalho de evento-resumo
Aldol reaction by lipase from Rhizopus Niveus (2017)
Birolli, Willian Garcia; Fonseca, Luis P; Porto, Andre Luiz Meleiro
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: LIPASE
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ABNT
BIROLLI, Willian Garcia e FONSECA, Luis P e PORTO, Andre Luiz Meleiro. Aldol reaction by lipase from Rhizopus Niveus. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/239c26f3-9990-4b2d-ab95-944e5c00e7a3/P16982.pdf. Acesso em: 01 maio 2026.
APA
Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2017). Aldol reaction by lipase from Rhizopus Niveus. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/239c26f3-9990-4b2d-ab95-944e5c00e7a3/P16982.pdf
NLM
Birolli WG, Fonseca LP, Porto ALM. Aldol reaction by lipase from Rhizopus Niveus [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/239c26f3-9990-4b2d-ab95-944e5c00e7a3/P16982.pdf
Vancouver
Birolli WG, Fonseca LP, Porto ALM. Aldol reaction by lipase from Rhizopus Niveus [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/239c26f3-9990-4b2d-ab95-944e5c00e7a3/P16982.pdf
Trabalho de evento-resumo
OH insertion reactions catalised by bronsted acid (2017)
Gallo, Rafael D. C; Burtoloso, Antonio Carlos Bender
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
GALLO, Rafael D. C e BURTOLOSO, Antonio Carlos Bender. OH insertion reactions catalised by bronsted acid. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf. Acesso em: 01 maio 2026.
APA
Gallo, R. D. C., & Burtoloso, A. C. B. (2017). OH insertion reactions catalised by bronsted acid. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf
NLM
Gallo RDC, Burtoloso ACB. OH insertion reactions catalised by bronsted acid [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf
Vancouver
Gallo RDC, Burtoloso ACB. OH insertion reactions catalised by bronsted acid [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf
Trabalho de evento-resumo
Development of self-assembled monolayer of thiol on gold electrodes and application for the in situ formation of gold nanoparticles (2017)
Sanz, Caroline G; Bacil, Raphael Prata; Campos, O S; Buoro, Rafael Martos ; Serrano, Silvia Helena Pires
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidades: IQSC, IQ
Assunto: ELETRODO
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ABNT
SANZ, Caroline G et al. Development of self-assembled monolayer of thiol on gold electrodes and application for the in situ formation of gold nanoparticles. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/9b9d6a9a-4cac-43b6-ab75-6be054873e92/P16984.pdf. Acesso em: 01 maio 2026.
APA
Sanz, C. G., Bacil, R. P., Campos, O. S., Buoro, R. M., & Serrano, S. H. P. (2017). Development of self-assembled monolayer of thiol on gold electrodes and application for the in situ formation of gold nanoparticles. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/9b9d6a9a-4cac-43b6-ab75-6be054873e92/P16984.pdf
NLM
Sanz CG, Bacil RP, Campos OS, Buoro RM, Serrano SHP. Development of self-assembled monolayer of thiol on gold electrodes and application for the in situ formation of gold nanoparticles [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/9b9d6a9a-4cac-43b6-ab75-6be054873e92/P16984.pdf
Vancouver
Sanz CG, Bacil RP, Campos OS, Buoro RM, Serrano SHP. Development of self-assembled monolayer of thiol on gold electrodes and application for the in situ formation of gold nanoparticles [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/9b9d6a9a-4cac-43b6-ab75-6be054873e92/P16984.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
Source: Proceedings. Conference titles: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/7b413a71-f750-452b-85ba-f7dbf425db85/P16985.pdf
Trabalho de evento-resumo
Metabolomics of the Nudibranch Roboatra ernsti (2017)
Takaki, Mirelle; Padula, Vinicius; Berlinck, Roberto Gomes de Souza
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: ALCALOIDES
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ABNT
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: 01 maio 2026.
APA
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/60bc5630-7945-4ebd-af85-18ea2f6bae80/P16987.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
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Subjects: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/aebadad2-ba19-4069-b907-86b8e9fa45fa/P16983.pdf
Trabalho de evento-resumo
Brominated secondary metabolites produced by the marine bacterium Pseudovibrio denitrificans Ab134 (2017)
Nicacio, Karen J; Ióca, Laura P; Thompson, Fabiano; Ferreira, Antonio G; Berlinck, Roberto Gomes de Souza
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Subjects: BACTÉRIAS, BIOLOGIA MARINHA
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ABNT
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: 01 maio 2026.
APA
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/930c05c6-ca5b-4b49-8c8d-ea13342fe9f4/P16992.pdf
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
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidades: IQ, IQSC
Subjects: ANALGÉSICOS, ELETROQUÍMICA
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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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/a1024c9d-42b7-4bc2-b345-10b100af8f62/P16997.pdf
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
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Subjects: PRODUTOS NATURAIS, FUNGICIDAS
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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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/3426468f-204b-4c3d-a4dc-ee893604db54/P17001.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
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Subjects: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
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
Source: Proceedings. Conference titles: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] 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
Source: Proceedings. Conference titles: 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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Increasing coverage in shotgun proteomics in the SCXxRP-MS/MS method (2017)
Batiston, Weliton Pedro; Santos Neto, Alvaro Jose dos ; Carrilho, Emanuel
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Subjects: PROTEÍNAS, ESPECTROSCOPIA DE MASSA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 01 maio 2026.
APA
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
NLM
Batiston WP, Santos Neto AJ dos, Carrilho E. Increasing coverage in shotgun proteomics in the SCXxRP-MS/MS method [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/4f1fe388-da69-4e2b-aa7b-39614a62b784/P16970.pdf
Trabalho de evento-resumo
Thermal decomposition of some inosine 5'-monophosphate salts (2017)
De Jesus, Jany Hellen Ferreira ; Ferreira, Ana Paula Garcia; Cavalheiro, Eder Tadeu Gomes
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: ANÁLISE TÉRMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DE JESUS, Jany Hellen Ferreira e FERREIRA, Ana Paula Garcia e CAVALHEIRO, Eder Tadeu Gomes. Thermal decomposition of some inosine 5'-monophosphate salts. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/80a7652b-bf8c-4770-b170-c0e1e7607e9f/P16973.pdf. Acesso em: 01 maio 2026.
APA
De Jesus, J. H. F., Ferreira, A. P. G., & Cavalheiro, E. T. G. (2017). Thermal decomposition of some inosine 5'-monophosphate salts. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/80a7652b-bf8c-4770-b170-c0e1e7607e9f/P16973.pdf
NLM
De Jesus JHF, Ferreira APG, Cavalheiro ETG. Thermal decomposition of some inosine 5'-monophosphate salts [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/80a7652b-bf8c-4770-b170-c0e1e7607e9f/P16973.pdf
Vancouver
De Jesus JHF, Ferreira APG, Cavalheiro ETG. Thermal decomposition of some inosine 5'-monophosphate salts [Internet]. Proceedings. 2017 ;[citado 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/80a7652b-bf8c-4770-b170-c0e1e7607e9f/P16973.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
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Subjects: ELETRODO, OXIGÊNIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 maio 2026.
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 2026 maio 01 ] 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 2026 maio 01 ] Available from: https://repositorio.usp.br/directbitstream/97f2357b-d59e-44b9-893a-c158dfbf7d43/P16974.pdf

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