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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
Trabalho de evento-resumo periodico
Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations (2019)
Silva, Vitor Hugo Menezes da ; Oliveira, Caio C; Correia, Carlos Roque Duarte; Braga, Ataualpa Albert Carmo
Source: Investigação. Conference titles: School of Computational Chemistry Modeling in Supramolecular Chemistry. Unidade: IQ
Subjects: LIGANTES, CATÁLISE
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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. Investigação. Franca: Instituto de Química, Universidade de São Paulo. Disponível em: http://3qc.iqm.unicamp.br/eqc/. Acesso em: 08 out. 2024. , 2019
APA
Silva, V. H. M. da, Oliveira, C. C., Correia, C. R. D., & Braga, A. A. C. (2019). Heck arylation of acyclic olefins employing arenediazonium salts and chiral N,N ligands: new mechanistic insights from quantum-chemical calculations. Investigação. Franca: Instituto de Química, Universidade de São Paulo. Recuperado de http://3qc.iqm.unicamp.br/eqc/
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]. Investigação. 2019 ; 18( p.):[citado 2024 out. 08 ] Available from: http://3qc.iqm.unicamp.br/eqc/
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]. Investigação. 2019 ; 18( p.):[citado 2024 out. 08 ] Available from: http://3qc.iqm.unicamp.br/eqc/
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 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
(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
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
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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
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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
Trabalho de evento-resumo
Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study (2015)
Servilha, Bruno Moraes; Correia, Carlos Roque Duarte; Braga, Ataualpa Albert Carmo
Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química/SBQ. Unidade: IQ
Assunto: REAÇÕES QUÍMICAS
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ABNT
SERVILHA, Bruno Moraes e CORREIA, Carlos Roque Duarte e BRAGA, Ataualpa Albert Carmo. Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study. 2015, Anais.. São Paulo: Sociedade Brasileira de Química/SBQ, 2015. Disponível em: http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf. Acesso em: 08 out. 2024.
APA
Servilha, B. M., Correia, C. R. D., & Braga, A. A. C. (2015). Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study. In Resumos. São Paulo: Sociedade Brasileira de Química/SBQ. Recuperado de http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf
NLM
Servilha BM, Correia CRD, Braga AAC. Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study [Internet]. Resumos. 2015 ;[citado 2024 out. 08 ] Available from: http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf
Vancouver
Servilha BM, Correia CRD, Braga AAC. Regioselectivity in an intramolecular Heck-Matsuda reactions: a DFT study [Internet]. Resumos. 2015 ;[citado 2024 out. 08 ] Available from: http://www.adaltech.com.br/testes/sbq2015/resumos/T0142-1.pdf
Trabalho de evento-resumo
Substrate control in an intramolecular heck-matsuda reaction: a DFT study (2015)
Servilha, Bruno Moraes; Correia, Carlos Roque Duarte; Braga, Ataualpa Albert Carmo
Source: Resumos. Conference titles: Simpósio Brasileiro de Química Teórica (SBQT). Unidade: IQ
Assunto: COMPOSTOS HETEROCÍCLICOS
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ABNT
SERVILHA, Bruno Moraes e CORREIA, Carlos Roque Duarte e BRAGA, Ataualpa Albert Carmo. Substrate control in an intramolecular heck-matsuda reaction: a DFT study. 2015, Anais.. Pirenópolis: Instituto de Química, Universidade de São Paulo, 2015. . Acesso em: 08 out. 2024.
APA
Servilha, B. M., Correia, C. R. D., & Braga, A. A. C. (2015). Substrate control in an intramolecular heck-matsuda reaction: a DFT study. In Resumos. Pirenópolis: Instituto de Química, Universidade de São Paulo.
NLM
Servilha BM, Correia CRD, Braga AAC. Substrate control in an intramolecular heck-matsuda reaction: a DFT study. Resumos. 2015 ;[citado 2024 out. 08 ]
Vancouver
Servilha BM, Correia CRD, Braga AAC. Substrate control in an intramolecular heck-matsuda reaction: a DFT study. Resumos. 2015 ;[citado 2024 out. 08 ]
Trabalho de evento-resumo
Solvent and substrate effects on the stereoselective Heck arylations of 3-cyclopentenol (2015)
Angnes, Ricardo Almir; Oliveira, Juliana M. de; Silva, Vitor Hugo Menezes da; Servilha, Bruno Moraes; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: Abstracts. Conference titles: Brazilian Meeting on Organic Synthesis (BMOS). Unidade: IQ
Subjects: SOLVENTE, CATÁLISE
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ABNT
ANGNES, Ricardo Almir et al. Solvent and substrate effects on the stereoselective Heck arylations of 3-cyclopentenol. 2015, Anais.. Búzios: Instituto de Química, Universidade de São Paulo, 2015. Disponível em: http://www.bmos.com.br/Upload/BMOS2015_201573112125.pdf. Acesso em: 08 out. 2024.
APA
Angnes, R. A., Oliveira, J. M. de, Silva, V. H. M. da, Servilha, B. M., Braga, A. A. C., & Correia, C. R. D. (2015). Solvent and substrate effects on the stereoselective Heck arylations of 3-cyclopentenol. In Abstracts. Búzios: Instituto de Química, Universidade de São Paulo. Recuperado de http://www.bmos.com.br/Upload/BMOS2015_201573112125.pdf
NLM
Angnes RA, Oliveira JM de, Silva VHM da, Servilha BM, Braga AAC, Correia CRD. Solvent and substrate effects on the stereoselective Heck arylations of 3-cyclopentenol [Internet]. Abstracts. 2015 ;[citado 2024 out. 08 ] Available from: http://www.bmos.com.br/Upload/BMOS2015_201573112125.pdf
Vancouver
Angnes RA, Oliveira JM de, Silva VHM da, Servilha BM, Braga AAC, Correia CRD. Solvent and substrate effects on the stereoselective Heck arylations of 3-cyclopentenol [Internet]. Abstracts. 2015 ;[citado 2024 out. 08 ] Available from: http://www.bmos.com.br/Upload/BMOS2015_201573112125.pdf
Trabalho de evento-resumo
Investigação teórica sobre a etapa de adição oxidativa dos ciclos catalíticos das reações de Heck-Matsuda e Heck-Mizoroki (2014)
Silva, Vitor Hugo Menezes da; Correia, Carlos Roque Duarte; Morgon, Nelson Henrique; Braga, Ataualpa Albert Carmo
Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química (SBQ). Unidade: IQ
Subjects: REAÇÕES ORGÂNICAS, CATÁLISE
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ABNT
SILVA, Vitor Hugo Menezes da et al. Investigação teórica sobre a etapa de adição oxidativa dos ciclos catalíticos das reações de Heck-Matsuda e Heck-Mizoroki. 2014, Anais.. São Paulo: Sociedade Brasileira de Química (SBQ), 2014. . Acesso em: 08 out. 2024.
APA
Silva, V. H. M. da, Correia, C. R. D., Morgon, N. H., & Braga, A. A. C. (2014). Investigação teórica sobre a etapa de adição oxidativa dos ciclos catalíticos das reações de Heck-Matsuda e Heck-Mizoroki. In Resumos. São Paulo: Sociedade Brasileira de Química (SBQ).
NLM
Silva VHM da, Correia CRD, Morgon NH, Braga AAC. Investigação teórica sobre a etapa de adição oxidativa dos ciclos catalíticos das reações de Heck-Matsuda e Heck-Mizoroki. Resumos. 2014 ;[citado 2024 out. 08 ]
Vancouver
Silva VHM da, Correia CRD, Morgon NH, Braga AAC. Investigação teórica sobre a etapa de adição oxidativa dos ciclos catalíticos das reações de Heck-Matsuda e Heck-Mizoroki. Resumos. 2014 ;[citado 2024 out. 08 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
Trabalho de evento-resumo
Síntese de novos 'beta'-aminoálcoois quirais via reação de Heck: aplicação na arilação enantiosseletiva de aldeídos (2009)
Moro, Angélica Venturini; Correia, Carlos Roque Duarte; Lüdtke, Diogo, Seibert
Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química. Unidade: FCF
Subjects: QUÍMICA ORGÂNICA, ALDEÍDOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORO, Angélica Venturini e CORREIA, Carlos Roque Duarte e LÜDTKE, Diogo. Síntese de novos 'beta'-aminoálcoois quirais via reação de Heck: aplicação na arilação enantiosseletiva de aldeídos. 2009, Anais.. São Paulo: SBQ, 2009. . Acesso em: 08 out. 2024.
APA
Moro, A. V., Correia, C. R. D., & Lüdtke, D. (2009). Síntese de novos 'beta'-aminoálcoois quirais via reação de Heck: aplicação na arilação enantiosseletiva de aldeídos. In Resumos. São Paulo: SBQ.
NLM
Moro AV, Correia CRD, Lüdtke D. Síntese de novos 'beta'-aminoálcoois quirais via reação de Heck: aplicação na arilação enantiosseletiva de aldeídos. Resumos. 2009 ;[citado 2024 out. 08 ]
Vancouver
Moro AV, Correia CRD, Lüdtke D. Síntese de novos 'beta'-aminoálcoois quirais via reação de Heck: aplicação na arilação enantiosseletiva de aldeídos. Resumos. 2009 ;[citado 2024 out. 08 ]
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
Artigo de periodico
Polymer solar cells using single-wall carbon nanotubes modified with thiophene pedant groups (2007)
Nogueira, Ana Flávia; Lomba, Bruno S.; Soto-Oviedo, Mauro A.; Correia, Carlos Roque Duarte; Corio, Paola ; Furtado, Clascídia A.; Hümmelgen, Ivo Alexandre
Source: Journal of Physical Chemistry C. Unidade: IQ
Subjects: NANOTECNOLOGIA, CÉLULAS SOLARES
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ABNT
NOGUEIRA, Ana Flávia et al. Polymer solar cells using single-wall carbon nanotubes modified with thiophene pedant groups. Journal of Physical Chemistry C, v. 111, n. 49, p. 18431-18438, 2007Tradução . . Acesso em: 08 out. 2024.
APA
Nogueira, A. F., Lomba, B. S., Soto-Oviedo, M. A., Correia, C. R. D., Corio, P., Furtado, C. A., & Hümmelgen, I. A. (2007). Polymer solar cells using single-wall carbon nanotubes modified with thiophene pedant groups. Journal of Physical Chemistry C, 111( 49), 18431-18438.
NLM
Nogueira AF, Lomba BS, Soto-Oviedo MA, Correia CRD, Corio P, Furtado CA, Hümmelgen IA. Polymer solar cells using single-wall carbon nanotubes modified with thiophene pedant groups. Journal of Physical Chemistry C. 2007 ; 111( 49): 18431-18438.[citado 2024 out. 08 ]
Vancouver
Nogueira AF, Lomba BS, Soto-Oviedo MA, Correia CRD, Corio P, Furtado CA, Hümmelgen IA. Polymer solar cells using single-wall carbon nanotubes modified with thiophene pedant groups. Journal of Physical Chemistry C. 2007 ; 111( 49): 18431-18438.[citado 2024 out. 08 ]

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