ReP USP - Resultado da busca

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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1002/ejoc.202200377
Artigo de periodico
Palladium-catalyzed sabinene oxidation with hydrogen peroxide: Smart fragrance production and DFT insights (2022)
Vieira, Camila Grossi ; Angnes, Ricardo Almir ; Braga, Ataualpa Albert Carmo ; Gusevskaya, Elena V; Rossi, Liane Marcia
Source: Molecular Catalysis. Unidade: IQ
Subjects: OXIDAÇÃO, PALÁDIO, PERÓXIDO DE HIDROGÊNIO
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ABNT
VIEIRA, Camila Grossi et al. Palladium-catalyzed sabinene oxidation with hydrogen peroxide: Smart fragrance production and DFT insights. Molecular Catalysis, v. 517, p. 1-8, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.mcat.2021.112033. Acesso em: 03 jun. 2024.
APA
Vieira, C. G., Angnes, R. A., Braga, A. A. C., Gusevskaya, E. V., & Rossi, L. M. (2022). Palladium-catalyzed sabinene oxidation with hydrogen peroxide: Smart fragrance production and DFT insights. Molecular Catalysis, 517, 1-8. doi:10.1016/j.mcat.2021.112033
NLM
Vieira CG, Angnes RA, Braga AAC, Gusevskaya EV, Rossi LM. Palladium-catalyzed sabinene oxidation with hydrogen peroxide: Smart fragrance production and DFT insights [Internet]. Molecular Catalysis. 2022 ; 517 1-8.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.mcat.2021.112033
Vancouver
Vieira CG, Angnes RA, Braga AAC, Gusevskaya EV, Rossi LM. Palladium-catalyzed sabinene oxidation with hydrogen peroxide: Smart fragrance production and DFT insights [Internet]. Molecular Catalysis. 2022 ; 517 1-8.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.mcat.2021.112033
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1002/adsc.201901471
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1002/chem.201801910
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: http://www.bmos.com.br/Upload/BMOS2015_201573112125.pdf

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