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Artigo de periodico
Mechanisms for the oxidative addition of palladium(0) complexes to arenediazonium salts (2023)
Esteves, Henrique; Silva, Vitor Hugo Menezes da ; Correia, Carlos Roque Duarte ; Braga, Ataualpa Albert Carmo
Source: Organometallics. Unidade: IQ
Subjects: COMPOSTOS AROMÁTICOS, LIGANTES, PALÁDIO
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ABNT
ESTEVES, Henrique et al. Mechanisms for the oxidative addition of palladium(0) complexes to arenediazonium salts. Organometallics, v. 42, n. 22, p. 3178-3191, 2023Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.organomet.3c00264. Acesso em: 08 out. 2024.
APA
Esteves, H., Silva, V. H. M. da, Correia, C. R. D., & Braga, A. A. C. (2023). Mechanisms for the oxidative addition of palladium(0) complexes to arenediazonium salts. Organometallics, 42( 22), 3178-3191. doi:10.1021/acs.organomet.3c00264
NLM
Esteves H, Silva VHM da, Correia CRD, Braga AAC. Mechanisms for the oxidative addition of palladium(0) complexes to arenediazonium salts [Internet]. Organometallics. 2023 ; 42( 22): 3178-3191.[citado 2024 out. 08 ] Available from: https://dx.doi.org/10.1021/acs.organomet.3c00264
Vancouver
Esteves H, Silva VHM da, Correia CRD, Braga AAC. Mechanisms for the oxidative addition of palladium(0) complexes to arenediazonium salts [Internet]. Organometallics. 2023 ; 42( 22): 3178-3191.[citado 2024 out. 08 ] Available from: https://dx.doi.org/10.1021/acs.organomet.3c00264
Artigo de periodico
Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams (2022)
Braga, Ingredy Bastos; Angnes, Ricardo Almir ; Lucca Júnior, Emílio Carlos de; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: European Journal of Organic Chemistry. Unidade: IQ
Subjects: PRODUTOS NATURAIS, LIGANTES
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ABNT
BRAGA, Ingredy Bastos et al. Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams. European Journal of Organic Chemistry, v. 26, n. 39, p. 1-8, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200377. Acesso em: 08 out. 2024.
APA
Braga, I. B., Angnes, R. A., Lucca Júnior, E. C. de, Braga, A. A. C., & Correia, C. R. D. (2022). Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams. European Journal of Organic Chemistry, 26( 39), 1-8. doi:10.1002/ejoc.202200377
NLM
Braga IB, Angnes RA, Lucca Júnior EC de, Braga AAC, Correia CRD. Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams [Internet]. European Journal of Organic Chemistry. 2022 ; 26( 39): 1-8.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/ejoc.202200377
Vancouver
Braga IB, Angnes RA, Lucca Júnior EC de, Braga AAC, Correia CRD. Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams [Internet]. European Journal of Organic Chemistry. 2022 ; 26( 39): 1-8.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/ejoc.202200377
Artigo de periodico
Reactive Phenanthrene Derivatives as Markers of Amino Groups in Fluorescence Microscopy of Surface Modified Micro-Zeolite L (2021)
Reis, Izadora Fonseca; Foltran, Larissa Schumekel; Lauer, Milena Helmer; Gehlen, Marcelo Henrique ; Drekener, Roberta Lopes; Correia, Carlos Roque Duarte
Source: Journal of Fluorescence. Unidade: IQSC
Subjects: FLUORESCÊNCIA, MICROSCOPIA
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ABNT
REIS, Izadora Fonseca et al. Reactive Phenanthrene Derivatives as Markers of Amino Groups in Fluorescence Microscopy of Surface Modified Micro-Zeolite L. Journal of Fluorescence, v. 31, n. 5, p. 1417-1424, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10895-021-02773-6. Acesso em: 08 out. 2024.
APA
Reis, I. F., Foltran, L. S., Lauer, M. H., Gehlen, M. H., Drekener, R. L., & Correia, C. R. D. (2021). Reactive Phenanthrene Derivatives as Markers of Amino Groups in Fluorescence Microscopy of Surface Modified Micro-Zeolite L. Journal of Fluorescence, 31( 5), 1417-1424. doi:10.1007/s10895-021-02773-6
NLM
Reis IF, Foltran LS, Lauer MH, Gehlen MH, Drekener RL, Correia CRD. Reactive Phenanthrene Derivatives as Markers of Amino Groups in Fluorescence Microscopy of Surface Modified Micro-Zeolite L [Internet]. Journal of Fluorescence. 2021 ; 31( 5): 1417-1424.[citado 2024 out. 08 ] Available from: https://doi.org/10.1007/s10895-021-02773-6
Vancouver
Reis IF, Foltran LS, Lauer MH, Gehlen MH, Drekener RL, Correia CRD. Reactive Phenanthrene Derivatives as Markers of Amino Groups in Fluorescence Microscopy of Surface Modified Micro-Zeolite L [Internet]. Journal of Fluorescence. 2021 ; 31( 5): 1417-1424.[citado 2024 out. 08 ] Available from: https://doi.org/10.1007/s10895-021-02773-6
Artigo de periodico
Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity (2020)
Polo, Ellen Christine; Wang, Martí Fernández; Angnes, Ricardo Almir; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: Advanced Synthesis and Catalysis. Unidade: IQ
Subjects: CATÁLISE ASSIMÉTRICA, REAÇÕES QUÍMICAS, PALÁDIO
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ABNT
POLO, Ellen Christine et al. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, v. 362, p. 884 – 892, 2020Tradução . . Disponível em: https://doi.org/10.1002/adsc.201901471. Acesso em: 08 out. 2024.
APA
Polo, E. C., Wang, M. F., Angnes, R. A., Braga, A. A. C., & Correia, C. R. D. (2020). Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, 362, 884 – 892. doi:10.1002/adsc.201901471
NLM
Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/adsc.201901471
Vancouver
Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/adsc.201901471
Artigo de periodico
Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations (2020)
Silva, Vitor Hugo Menezes da ; Oliveira, Caio C ; Correia, Carlos Roque Duarte ; Braga, Ataualpa Albert Carmo
Source: Theoretical Chemistry Accounts. Unidade: IQ
Subjects: CATÁLISE, LIGANTES
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ABNT
SILVA, Vitor Hugo Menezes da et al. Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations. Theoretical Chemistry Accounts, v. 139, p. 1-13 art. 77, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00214-020-02588-x. Acesso em: 08 out. 2024.
APA
Silva, V. H. M. da, Oliveira, C. C., Correia, C. R. D., & Braga, A. A. C. (2020). Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations. Theoretical Chemistry Accounts, 139, 1-13 art. 77. doi:10.1007/s00214-020-02588-x
NLM
Silva VHM da, Oliveira CC, Correia CRD, Braga AAC. Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations [Internet]. Theoretical Chemistry Accounts. 2020 ; 139 1-13 art. 77.[citado 2024 out. 08 ] Available from: https://doi.org/10.1007/s00214-020-02588-x
Vancouver
Silva VHM da, Oliveira CC, Correia CRD, Braga AAC. Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations [Internet]. Theoretical Chemistry Accounts. 2020 ; 139 1-13 art. 77.[citado 2024 out. 08 ] Available from: https://doi.org/10.1007/s00214-020-02588-x
Artigo de jornal-dep/entr
Criada molécula capaz de matar um dos parasitas da malária [Depoimento a Luis Sevillano] (2018)
Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte; Garcia, Célia Regina da Silva
Source: El País. Unidades: IFSC, IB
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, MALÁRIA, PLASMODIUM FALCIPARUM
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ABNT
GUIDO, Rafael Victorio Carvalho e CORREIA, Carlos Roque Duarte e GARCIA, Célia Regina da Silva. Criada molécula capaz de matar um dos parasitas da malária [Depoimento a Luis Sevillano]. El País. Madrid: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://brasil.elpais.com/brasil/2018/08/10/ciencia/1533927544_473818.html. Acesso em: 08 out. 2024. , 2018
APA
Guido, R. V. C., Correia, C. R. D., & Garcia, C. R. da S. (2018). Criada molécula capaz de matar um dos parasitas da malária [Depoimento a Luis Sevillano]. El País. Madrid: Instituto de Física de São Carlos, Universidade de São Paulo. Recuperado de https://brasil.elpais.com/brasil/2018/08/10/ciencia/1533927544_473818.html
NLM
Guido RVC, Correia CRD, Garcia CR da S. Criada molécula capaz de matar um dos parasitas da malária [Depoimento a Luis Sevillano] [Internet]. El País. 2018 ;[citado 2024 out. 08 ] Available from: https://brasil.elpais.com/brasil/2018/08/10/ciencia/1533927544_473818.html
Vancouver
Guido RVC, Correia CRD, Garcia CR da S. Criada molécula capaz de matar um dos parasitas da malária [Depoimento a Luis Sevillano] [Internet]. El País. 2018 ;[citado 2024 out. 08 ] Available from: https://brasil.elpais.com/brasil/2018/08/10/ciencia/1533927544_473818.html
Artigo de jornal-dep/entr
Informan de fuerte candidata para desarrollo de nuevo fármaco contra malaria, fue capaz de matar incluso a cepa resistente a antipalúdicos convencionales [Depoimento] (2018)
Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte; Garcia, Célia Regina da Silva
Source: Plenilunia. Unidades: IFSC, IB
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, MALÁRIA, PLASMODIUM FALCIPARUM
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ABNT
GUIDO, Rafael Victorio Carvalho e CORREIA, Carlos Roque Duarte e GARCIA, Célia Regina da Silva. Informan de fuerte candidata para desarrollo de nuevo fármaco contra malaria, fue capaz de matar incluso a cepa resistente a antipalúdicos convencionales [Depoimento]. Plenilunia. Ciudad de México: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://plenilunia.com/novedades-medicas/informan-de-fuerte-candidata-para-desarrollo-de-nuevo-farmaco-contra-malaria-fue-capaz-de-matar-incluso-a-cepa-resistente-a-antipaludicos-convencionales/56684/. Acesso em: 08 out. 2024. , 2018
APA
Guido, R. V. C., Correia, C. R. D., & Garcia, C. R. da S. (2018). Informan de fuerte candidata para desarrollo de nuevo fármaco contra malaria, fue capaz de matar incluso a cepa resistente a antipalúdicos convencionales [Depoimento]. Plenilunia. Ciudad de México: Instituto de Física de São Carlos, Universidade de São Paulo. Recuperado de https://plenilunia.com/novedades-medicas/informan-de-fuerte-candidata-para-desarrollo-de-nuevo-farmaco-contra-malaria-fue-capaz-de-matar-incluso-a-cepa-resistente-a-antipaludicos-convencionales/56684/
NLM
Guido RVC, Correia CRD, Garcia CR da S. Informan de fuerte candidata para desarrollo de nuevo fármaco contra malaria, fue capaz de matar incluso a cepa resistente a antipalúdicos convencionales [Depoimento] [Internet]. Plenilunia. 2018 ;[citado 2024 out. 08 ] Available from: https://plenilunia.com/novedades-medicas/informan-de-fuerte-candidata-para-desarrollo-de-nuevo-farmaco-contra-malaria-fue-capaz-de-matar-incluso-a-cepa-resistente-a-antipaludicos-convencionales/56684/
Vancouver
Guido RVC, Correia CRD, Garcia CR da S. Informan de fuerte candidata para desarrollo de nuevo fármaco contra malaria, fue capaz de matar incluso a cepa resistente a antipalúdicos convencionales [Depoimento] [Internet]. Plenilunia. 2018 ;[citado 2024 out. 08 ] Available from: https://plenilunia.com/novedades-medicas/informan-de-fuerte-candidata-para-desarrollo-de-nuevo-farmaco-contra-malaria-fue-capaz-de-matar-incluso-a-cepa-resistente-a-antipaludicos-convencionales/56684/
Artigo de periodico
(1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis (2018)
Zukerman-Schpector, Júlio; Monsalve, Monica Soto; Santos, Regina Helena de Almeida; Machado, Angelo H L; Correia, Carlos Roque Duarte; Jotani , Mukesh M; Tiekink, Edward R T
Source: Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. Unidade: IQSC
Assunto: CRISTALOGRAFIA
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ABNT
ZUKERMAN-SCHPECTOR, Júlio et al. (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, v. E74, p. 414-418, 2018Tradução . . Disponível em: https://doi.org/10.1107/S2056989018003092. Acesso em: 08 out. 2024.
APA
Zukerman-Schpector, J., Monsalve, M. S., Santos, R. H. de A., Machado, A. H. L., Correia, C. R. D., Jotani , M. M., & Tiekink, E. R. T. (2018). (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, E74, 414-418. doi:10.1107/S2056989018003092
NLM
Zukerman-Schpector J, Monsalve MS, Santos RH de A, Machado AHL, Correia CRD, Jotani MM, Tiekink ERT. (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; E74 414-418.[citado 2024 out. 08 ] Available from: https://doi.org/10.1107/S2056989018003092
Vancouver
Zukerman-Schpector J, Monsalve MS, Santos RH de A, Machado AHL, Correia CRD, Jotani MM, Tiekink ERT. (1 R ,2 S ,5 R )-5-Methyl-2-[2-(4-nitrophenyl)propan-2- yl]cyclohexyl 2-(4-methoxyphenyl)-2,5-dihydro- 1 H -pyrrole-1-carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; E74 414-418.[citado 2024 out. 08 ] Available from: https://doi.org/10.1107/S2056989018003092
Artigo de jornal-dep/entr
A new, highly effective and selective molecule is developed to fight malaria [Depoimento a Joao Carlos da Silva] (2018)
Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte; Garcia, Célia Regina da Silva
Source: Scienmag Science Magazine. Unidades: IFSC, IB
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, MALÁRIA, PLASMODIUM FALCIPARUM
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ABNT
GUIDO, Rafael Victorio Carvalho e CORREIA, Carlos Roque Duarte e GARCIA, Célia Regina da Silva. A new, highly effective and selective molecule is developed to fight malaria [Depoimento a Joao Carlos da Silva]. Scienmag Science Magazine. Pensilvânia: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://scienmag.com/a-new-highly-effective-and-selective-molecule-is-developed-to-fight-malaria/. Acesso em: 08 out. 2024. , 2018
APA
Guido, R. V. C., Correia, C. R. D., & Garcia, C. R. da S. (2018). A new, highly effective and selective molecule is developed to fight malaria [Depoimento a Joao Carlos da Silva]. Scienmag Science Magazine. Pensilvânia: Instituto de Física de São Carlos, Universidade de São Paulo. Recuperado de https://scienmag.com/a-new-highly-effective-and-selective-molecule-is-developed-to-fight-malaria/
NLM
Guido RVC, Correia CRD, Garcia CR da S. A new, highly effective and selective molecule is developed to fight malaria [Depoimento a Joao Carlos da Silva] [Internet]. Scienmag Science Magazine. 2018 ;[citado 2024 out. 08 ] Available from: https://scienmag.com/a-new-highly-effective-and-selective-molecule-is-developed-to-fight-malaria/
Vancouver
Guido RVC, Correia CRD, Garcia CR da S. A new, highly effective and selective molecule is developed to fight malaria [Depoimento a Joao Carlos da Silva] [Internet]. Scienmag Science Magazine. 2018 ;[citado 2024 out. 08 ] Available from: https://scienmag.com/a-new-highly-effective-and-selective-molecule-is-developed-to-fight-malaria/
Artigo de periodico
Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins (2018)
Oliveira, Juliana Manso de; Angnes, Ricardo Almir; Khan, Ismat Ullah; Polo, Ellen Christine; Heerdt, Gabriel; Servilha, Bruno M; Silva, Vitor H. Menezes da; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: Chemistry European Journal. Unidade: IQ
Subjects: CATÁLISE, PALÁDIO
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ABNT
OLIVEIRA, Juliana Manso de et al. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, v. 24, n. 45, p. 11738-11747, 2018Tradução . . Disponível em: https://doi.org/10.1002/chem.201801910. Acesso em: 08 out. 2024.
APA
Oliveira, J. M. de, Angnes, R. A., Khan, I. U., Polo, E. C., Heerdt, G., Servilha, B. M., et al. (2018). Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, 24( 45), 11738-11747. doi:10.1002/chem.201801910
NLM
Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/chem.201801910
Vancouver
Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/chem.201801910
Artigo de periodico
Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity (2018)
Aguiar, Anna Caroline Campos; Panciera, Michele; Santos, Eric Francisco Simão dos; Singh, Maneesh Kumar; Garcia, Mariana Lopes; Guido, Rafael Victorio Carvalho ; Souza, Guilherme Eduardo de; Nakabashi, Myna; Costa, José Luiz; Garcia, Célia Regina da Silva ; Oliva, Glaucius ; Correia, Carlos Roque Duarte; Guido, Rafael Victorio Carvalho
Source: Journal of Medicinal Chemistry. Unidades: IB, IFSC
Subjects: PLASMODIUM FALCIPARUM, MALÁRIA, PLANEJAMENTO DE FÁRMACOS
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ABNT
AGUIAR, Anna Caroline Campos et al. Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity. Journal of Medicinal Chemistry, v. 61, n. 13, p. 5547-5568, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.8b00143. Acesso em: 08 out. 2024.
APA
Aguiar, A. C. C., Panciera, M., Santos, E. F. S. dos, Singh, M. K., Garcia, M. L., Guido, R. V. C., et al. (2018). Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity. Journal of Medicinal Chemistry, 61( 13), 5547-5568. doi:10.1021/acs.jmedchem.8b00143
NLM
Aguiar ACC, Panciera M, Santos EFS dos, Singh MK, Garcia ML, Guido RVC, Souza GE de, Nakabashi M, Costa JL, Garcia CR da S, Oliva G, Correia CRD, Guido RVC. Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 13): 5547-5568.[citado 2024 out. 08 ] Available from: https://doi.org/10.1021/acs.jmedchem.8b00143
Vancouver
Aguiar ACC, Panciera M, Santos EFS dos, Singh MK, Garcia ML, Guido RVC, Souza GE de, Nakabashi M, Costa JL, Garcia CR da S, Oliva G, Correia CRD, Guido RVC. Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 13): 5547-5568.[citado 2024 out. 08 ] Available from: https://doi.org/10.1021/acs.jmedchem.8b00143
Artigo de periodico
(4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis (2018)
Zukerman-Schpector, Júlio; Monsalve, Monica Soto; Santos, Regina Helena de Almeida; Garcia, Ariel L L; Correia, Carlos Roque Duarte; Jotani , Mukesh M; Tiekink, Edward R T
Source: Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. Unidade: IQSC
Assunto: CRISTALOGRAFIA
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ABNT
ZUKERMAN-SCHPECTOR, Júlio et al. (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, p. 371-375, 2018Tradução . . Disponível em: https://doi.org/10.1107/S2056989018002451. Acesso em: 08 out. 2024.
APA
Zukerman-Schpector, J., Monsalve, M. S., Santos, R. H. de A., Garcia, A. L. L., Correia, C. R. D., Jotani , M. M., & Tiekink, E. R. T. (2018). (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS, 371-375. doi:10.1107/S2056989018002451
NLM
Zukerman-Schpector J, Monsalve MS, Santos RH de A, Garcia ALL, Correia CRD, Jotani MM, Tiekink ERT. (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; 371-375.[citado 2024 out. 08 ] Available from: https://doi.org/10.1107/S2056989018002451
Vancouver
Zukerman-Schpector J, Monsalve MS, Santos RH de A, Garcia ALL, Correia CRD, Jotani MM, Tiekink ERT. (4-Nitrophenyl)methyl 2,3-dihydro-1 H -pyrrole-1- carboxylate: crystal structure and Hirshfeld analysis [Internet]. Acta Crystallographica Section E CRYSTALLOGRAPHIC COMMUNICATIONS. 2018 ; 371-375.[citado 2024 out. 08 ] Available from: https://doi.org/10.1107/S2056989018002451
Artigo de jornal-dep/entr
A new, highly effective and selective molecule to fight malaria [Depoimento a Maria Fernanda Ziegler] (2018)
Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte; Garcia, Célia Regina da Silva
Source: Phys.org. Unidades: IFSC, IB
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, MALÁRIA, PLASMODIUM FALCIPARUM
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUIDO, Rafael Victorio Carvalho e CORREIA, Carlos Roque Duarte e GARCIA, Célia Regina da Silva. A new, highly effective and selective molecule to fight malaria [Depoimento a Maria Fernanda Ziegler]. Phys.org. Douglas: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://phys.org/news/2018-08-highly-effective-molecule-malaria.html. Acesso em: 08 out. 2024. , 2018
APA
Guido, R. V. C., Correia, C. R. D., & Garcia, C. R. da S. (2018). A new, highly effective and selective molecule to fight malaria [Depoimento a Maria Fernanda Ziegler]. Phys.org. Douglas: Instituto de Física de São Carlos, Universidade de São Paulo. Recuperado de https://phys.org/news/2018-08-highly-effective-molecule-malaria.html
NLM
Guido RVC, Correia CRD, Garcia CR da S. A new, highly effective and selective molecule to fight malaria [Depoimento a Maria Fernanda Ziegler] [Internet]. Phys.org. 2018 ;[citado 2024 out. 08 ] Available from: https://phys.org/news/2018-08-highly-effective-molecule-malaria.html
Vancouver
Guido RVC, Correia CRD, Garcia CR da S. A new, highly effective and selective molecule to fight malaria [Depoimento a Maria Fernanda Ziegler] [Internet]. Phys.org. 2018 ;[citado 2024 out. 08 ] Available from: https://phys.org/news/2018-08-highly-effective-molecule-malaria.html
Trabalho de evento-resumo
Marinoquinolines as antimalarial agents: design of new highly active and selective derivatives (2018)
Barbosa, Patrícia Santos; Santos, Eric Francisco Simão dos; Panciera, Michele; Aguiar, Anna Caroline Campos; Garcia, Mariana Lopes; Souza, Guilherme Eduardo de; Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte
Source: Book of Abstracts. Conference titles: Alpine Winter Conference on Medicinal and Synthetic Chemistry. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, MALÁRIA, PLASMODIUM FALCIPARUM
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, Patrícia Santos et al. Marinoquinolines as antimalarial agents: design of new highly active and selective derivatives. 2018, Anais.. Louvain-la-Neuve: European Federation for Medicinal Chemistry - EFMC, 2018. . Acesso em: 08 out. 2024.
APA
Barbosa, P. S., Santos, E. F. S. dos, Panciera, M., Aguiar, A. C. C., Garcia, M. L., Souza, G. E. de, et al. (2018). Marinoquinolines as antimalarial agents: design of new highly active and selective derivatives. In Book of Abstracts. Louvain-la-Neuve: European Federation for Medicinal Chemistry - EFMC.
NLM
Barbosa PS, Santos EFS dos, Panciera M, Aguiar ACC, Garcia ML, Souza GE de, Guido RVC, Correia CRD. Marinoquinolines as antimalarial agents: design of new highly active and selective derivatives. Book of Abstracts. 2018 ;[citado 2024 out. 08 ]
Vancouver
Barbosa PS, Santos EFS dos, Panciera M, Aguiar ACC, Garcia ML, Souza GE de, Guido RVC, Correia CRD. Marinoquinolines as antimalarial agents: design of new highly active and selective derivatives. Book of Abstracts. 2018 ;[citado 2024 out. 08 ]
Artigo de jornal-dep/entr
New laboratory-synthesized molecule appears to fight malaria effectively [Depoimento] (2018)
Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte; Garcia, Célia Regina da Silva
Source: News-Medical.Net. Unidades: IFSC, IB
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, MALÁRIA, PLASMODIUM FALCIPARUM
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUIDO, Rafael Victorio Carvalho e CORREIA, Carlos Roque Duarte e GARCIA, Célia Regina da Silva. New laboratory-synthesized molecule appears to fight malaria effectively [Depoimento]. News-Medical.Net. London: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://www.news-medical.net/news/20180810/New-laboratory-synthesized-molecule-appears-to-fight-malaria-effectively.aspx. Acesso em: 08 out. 2024. , 2018
APA
Guido, R. V. C., Correia, C. R. D., & Garcia, C. R. da S. (2018). New laboratory-synthesized molecule appears to fight malaria effectively [Depoimento]. News-Medical.Net. London: Instituto de Física de São Carlos, Universidade de São Paulo. Recuperado de https://www.news-medical.net/news/20180810/New-laboratory-synthesized-molecule-appears-to-fight-malaria-effectively.aspx
NLM
Guido RVC, Correia CRD, Garcia CR da S. New laboratory-synthesized molecule appears to fight malaria effectively [Depoimento] [Internet]. News-Medical.Net. 2018 ;[citado 2024 out. 08 ] Available from: https://www.news-medical.net/news/20180810/New-laboratory-synthesized-molecule-appears-to-fight-malaria-effectively.aspx
Vancouver
Guido RVC, Correia CRD, Garcia CR da S. New laboratory-synthesized molecule appears to fight malaria effectively [Depoimento] [Internet]. News-Medical.Net. 2018 ;[citado 2024 out. 08 ] Available from: https://www.news-medical.net/news/20180810/New-laboratory-synthesized-molecule-appears-to-fight-malaria-effectively.aspx
Trabalho de evento-resumo
Conformational preferences on the enantioselective Heck-Matsuda arylation of cyclopent-3-ylmethanol: a DFT study (2017)
Braga, Ataualpa Albert Carmo ; Servilha, Bruno Moraes; Silva, Vitor Hugo Menezes da; Angnes, Ricardo Almir; Oliveira, Juliana M. de; Correia, Carlos Roque Duarte
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: REAÇÕES ORGÂNICAS, PALÁDIO
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ABNT
BRAGA, Ataualpa Albert Carmo et al. Conformational preferences on the enantioselective Heck-Matsuda arylation of cyclopent-3-ylmethanol: a DFT study. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 08 out. 2024.
APA
Braga, A. A. C., Servilha, B. M., Silva, V. H. M. da, Angnes, R. A., Oliveira, J. M. de, & Correia, C. R. D. (2017). Conformational preferences on the enantioselective Heck-Matsuda arylation of cyclopent-3-ylmethanol: a DFT study. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Braga AAC, Servilha BM, Silva VHM da, Angnes RA, Oliveira JM de, Correia CRD. Conformational preferences on the enantioselective Heck-Matsuda arylation of cyclopent-3-ylmethanol: a DFT study [Internet]. Proceedings. 2017 ;[citado 2024 out. 08 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Braga AAC, Servilha BM, Silva VHM da, Angnes RA, Oliveira JM de, Correia CRD. Conformational preferences on the enantioselective Heck-Matsuda arylation of cyclopent-3-ylmethanol: a DFT study [Internet]. Proceedings. 2017 ;[citado 2024 out. 08 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates (2017)
Silva, Vitor Hugo Menezes da; Oliveira, Caio Cesar Spindola de; Correia, Carlos Roque Duarte; Braga, Ataualpa Albert Carmo
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Vitor Hugo Menezes da et al. DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 08 out. 2024.
APA
Silva, V. H. M. da, Oliveira, C. C. S. de, Correia, C. R. D., & Braga, A. A. C. (2017). DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Silva VHM da, Oliveira CCS de, Correia CRD, Braga AAC. DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates [Internet]. Proceedings. 2017 ;[citado 2024 out. 08 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Silva VHM da, Oliveira CCS de, Correia CRD, Braga AAC. DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates [Internet]. Proceedings. 2017 ;[citado 2024 out. 08 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Artigo de periodico
Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds (2016)
Silva, Juliana de Oliveira; Angnes, Ricardo A; Silva, Vitor Hugo Menezes da; Servilha, Bruno M; Adeel, Muhammad; Braga, Ataualpa Albert Carmo ; Aponick, Aaron; Correia, Carlos Roque Duarte
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: SOLVENTE, CATÁLISE, REAÇÕES QUÍMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Juliana de Oliveira et al. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, v. 81, n. 5, p. 2010-2018, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b02846. Acesso em: 08 out. 2024.
APA
Silva, J. de O., Angnes, R. A., Silva, V. H. M. da, Servilha, B. M., Adeel, M., Braga, A. A. C., et al. (2016). Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, 81( 5), 2010-2018. doi:10.1021/acs.joc.5b02846
NLM
Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 out. 08 ] Available from: https://doi.org/10.1021/acs.joc.5b02846
Vancouver
Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 out. 08 ] Available from: https://doi.org/10.1021/acs.joc.5b02846
Artigo de periodico
Chiral triphenylprolinol ligands for the efficient catalytic asymmetric arylation of aldehydes (2010)
Moro, Angélica Venturini; Tiekink, Edward R. T; Zukerman-Schpector, Júlio; Lüdtke, Diogo, Seibert; Correia, Carlos Roque Duarte
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: ALDEÍDOS, SÍNTESE ORGÂNICA
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ABNT
MORO, Angélica Venturini et al. Chiral triphenylprolinol ligands for the efficient catalytic asymmetric arylation of aldehydes. European Journal of Organic Chemistry, v. 2010, n. 19, p. 3696-3703, 2010Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201000336. Acesso em: 08 out. 2024.
APA
Moro, A. V., Tiekink, E. R. T., Zukerman-Schpector, J., Lüdtke, D., & Correia, C. R. D. (2010). Chiral triphenylprolinol ligands for the efficient catalytic asymmetric arylation of aldehydes. European Journal of Organic Chemistry, 2010( 19), 3696-3703. doi:10.1002/ejoc.201000336
NLM
Moro AV, Tiekink ERT, Zukerman-Schpector J, Lüdtke D, Correia CRD. Chiral triphenylprolinol ligands for the efficient catalytic asymmetric arylation of aldehydes [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 19): 3696-3703.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/ejoc.201000336
Vancouver
Moro AV, Tiekink ERT, Zukerman-Schpector J, Lüdtke D, Correia CRD. Chiral triphenylprolinol ligands for the efficient catalytic asymmetric arylation of aldehydes [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 19): 3696-3703.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/ejoc.201000336
Artigo de periodico
Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones (2008)
Burtoloso, Antonio Carlos Bender ; Correia, Carlos Roque Duarte
Source: Tetrahedron. Unidade: IQSC
Subjects: PRODUTOS NATURAIS, QUÍMICA, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURTOLOSO, Antonio Carlos Bender e CORREIA, Carlos Roque Duarte. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones. Tetrahedron, v. 64, n. 42, p. 9928-9936, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.08.001. Acesso em: 08 out. 2024.
APA
Burtoloso, A. C. B., & Correia, C. R. D. (2008). Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones. Tetrahedron, 64( 42), 9928-9936. doi:10.1016/j.tet.2008.08.001
NLM
Burtoloso ACB, Correia CRD. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones [Internet]. Tetrahedron. 2008 ; 64( 42): 9928-9936.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tet.2008.08.001
Vancouver
Burtoloso ACB, Correia CRD. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones [Internet]. Tetrahedron. 2008 ; 64( 42): 9928-9936.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tet.2008.08.001

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