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Artigo de periodico
Molecular construction using formamideas a C1 feedstock (2024)
Sacchelli, Bruce Alan Lobo ; Rocha, Bianca Campanile ; Fantinel, Mariane; Andrade, Leandro Helgueira
Source: European Journal of Organic Chemistry. Unidade: IQ
Subjects: COMPOSTOS ORGÂNICOS, SÍNTESE ORGÂNICA
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ABNT
SACCHELLI, Bruce Alan Lobo et al. Molecular construction using formamideas a C1 feedstock. European Journal of Organic Chemistry, v. 2024, p. 1-36 art. e202300930, 2024Tradução . . Disponível em: https://dx.doi.org/10.1002/ejoc.202300930. Acesso em: 06 jun. 2024.
APA
Sacchelli, B. A. L., Rocha, B. C., Fantinel, M., & Andrade, L. H. (2024). Molecular construction using formamideas a C1 feedstock. European Journal of Organic Chemistry, 2024, 1-36 art. e202300930. doi:10.1002/ejoc.202300930
NLM
Sacchelli BAL, Rocha BC, Fantinel M, Andrade LH. Molecular construction using formamideas a C1 feedstock [Internet]. European Journal of Organic Chemistry. 2024 ; 2024 1-36 art. e202300930.[citado 2024 jun. 06 ] Available from: https://dx.doi.org/10.1002/ejoc.202300930
Vancouver
Sacchelli BAL, Rocha BC, Fantinel M, Andrade LH. Molecular construction using formamideas a C1 feedstock [Internet]. European Journal of Organic Chemistry. 2024 ; 2024 1-36 art. e202300930.[citado 2024 jun. 06 ] Available from: https://dx.doi.org/10.1002/ejoc.202300930
Artigo de periodico
Expanding the Chemical Space of Non-Proteinogenic N4 - Substituted Asparagine: Racemic, Enantioenriched, and Deuterated Derivatives (2023)
Pissinati, Emanuele F.; Delgado, José A. C.; Moro, Pedro A. M.; Correia, José T. M.; Berlinck, Roberto Gomes de Souza ; Paixão, Marcio W.
Source: European Journal of Organic Chemistry. Unidade: IQSC
Subjects: AMINOÁCIDOS, PEPTÍDEOS
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ABNT
PISSINATI, Emanuele F. et al. Expanding the Chemical Space of Non-Proteinogenic N4 - Substituted Asparagine: Racemic, Enantioenriched, and Deuterated Derivatives. European Journal of Organic Chemistry, v. 26, p. e202300274, 2023Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202300274. Acesso em: 06 jun. 2024.
APA
Pissinati, E. F., Delgado, J. A. C., Moro, P. A. M., Correia, J. T. M., Berlinck, R. G. de S., & Paixão, M. W. (2023). Expanding the Chemical Space of Non-Proteinogenic N4 - Substituted Asparagine: Racemic, Enantioenriched, and Deuterated Derivatives. European Journal of Organic Chemistry, 26, e202300274. doi:10.1002/ejoc.202300274
NLM
Pissinati EF, Delgado JAC, Moro PAM, Correia JTM, Berlinck RG de S, Paixão MW. Expanding the Chemical Space of Non-Proteinogenic N4 - Substituted Asparagine: Racemic, Enantioenriched, and Deuterated Derivatives [Internet]. European Journal of Organic Chemistry. 2023 ;26 e202300274.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202300274
Vancouver
Pissinati EF, Delgado JAC, Moro PAM, Correia JTM, Berlinck RG de S, Paixão MW. Expanding the Chemical Space of Non-Proteinogenic N4 - Substituted Asparagine: Racemic, Enantioenriched, and Deuterated Derivatives [Internet]. European Journal of Organic Chemistry. 2023 ;26 e202300274.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202300274
Artigo de periodico
Visible-light-induced insertion of sulfur dioxide mediated by electron donor-acceptor complex: synthesis and photophysical properties of 3-sulfonyl indolizines (2023)
Naud-Martin, Delphine; Kosiuha, Marharyta; Cocca, Leandro Henrique Zucolotto ; Retailleau, Pascal; Mahuteau-Betzer, Florence; De Boni, Leonardo ; Piguel, Sandrine
Source: European Journal of Organic Chemistry. Unidade: IFSC
Subjects: FLUORESCÊNCIA, PROPRIEDADES DOS MATERIAIS, FOTOCATÁLISE
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ABNT
NAUD-MARTIN, Delphine et al. Visible-light-induced insertion of sulfur dioxide mediated by electron donor-acceptor complex: synthesis and photophysical properties of 3-sulfonyl indolizines. European Journal of Organic Chemistry, v. 26, n. 22, p. e202300125-1-e202300125-6 + supporting information: S1-S75, 2023Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202300125. Acesso em: 06 jun. 2024.
APA
Naud-Martin, D., Kosiuha, M., Cocca, L. H. Z., Retailleau, P., Mahuteau-Betzer, F., De Boni, L., & Piguel, S. (2023). Visible-light-induced insertion of sulfur dioxide mediated by electron donor-acceptor complex: synthesis and photophysical properties of 3-sulfonyl indolizines. European Journal of Organic Chemistry, 26( 22), e202300125-1-e202300125-6 + supporting information: S1-S75. doi:10.1002/ejoc.202300125
NLM
Naud-Martin D, Kosiuha M, Cocca LHZ, Retailleau P, Mahuteau-Betzer F, De Boni L, Piguel S. Visible-light-induced insertion of sulfur dioxide mediated by electron donor-acceptor complex: synthesis and photophysical properties of 3-sulfonyl indolizines [Internet]. European Journal of Organic Chemistry. 2023 ; 26( 22): e202300125-1-e202300125-6 + supporting information: S1-S75.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202300125
Vancouver
Naud-Martin D, Kosiuha M, Cocca LHZ, Retailleau P, Mahuteau-Betzer F, De Boni L, Piguel S. Visible-light-induced insertion of sulfur dioxide mediated by electron donor-acceptor complex: synthesis and photophysical properties of 3-sulfonyl indolizines [Internet]. European Journal of Organic Chemistry. 2023 ; 26( 22): e202300125-1-e202300125-6 + supporting information: S1-S75.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202300125
Artigo de periodico
Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds (2022)
Echemendía, Radell ; Jesus, Matheus Pereira de ; Furniel, Lucas G. ; Day, David Philip; Burtoloso, Antonio Carlos Bender
Source: European Journal of Organic Chemistry. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, OXIDAÇÃO, IODO
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ABNT
ECHEMENDÍA, Radell et al. Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds. European Journal of Organic Chemistry, v. 2022, n. 26, p. e202200441, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200441. Acesso em: 06 jun. 2024.
APA
Echemendía, R., Jesus, M. P. de, Furniel, L. G., Day, D. P., & Burtoloso, A. C. B. (2022). Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds. European Journal of Organic Chemistry, 2022( 26), e202200441. doi:10.1002/ejoc.202200441
NLM
Echemendía R, Jesus MP de, Furniel LG, Day DP, Burtoloso ACB. Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 26): e202200441.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202200441
Vancouver
Echemendía R, Jesus MP de, Furniel LG, Day DP, Burtoloso ACB. Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 26): e202200441.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202200441
Artigo de periodico
Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre (2022)
Zanin, Lucas Lima ; Matos, Thiago Kelvin Brito ; Leitão, Andrei ; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: European Journal of Organic Chemistry. Unidades: IQSC, IFSC
Subjects: CINÉTICA, HIDRÓLISE
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ABNT
ZANIN, Lucas Lima et al. Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre. European Journal of Organic Chemistry, v. 2022, n. 38, p. e202200331-1-e202200331-8, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200331. Acesso em: 06 jun. 2024.
APA
Zanin, L. L., Matos, T. K. B., Leitão, A., Ellena, J., & Porto, A. L. M. (2022). Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre. European Journal of Organic Chemistry, 2022( 38), e202200331-1-e202200331-8. doi:10.1002/ejoc.202200331
NLM
Zanin LL, Matos TKB, Leitão A, Ellena J, Porto ALM. Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 38): e202200331-1-e202200331-8.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202200331
Vancouver
Zanin LL, Matos TKB, Leitão A, Ellena J, Porto ALM. Biocatalytic kinetic resolution to access enantiomerically enriched dihydropyrimidinone/thiones via recognition of a remote stereocentre [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 38): e202200331-1-e202200331-8.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202200331
Artigo de periodico
Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction (2022)
Jesus, Jéssica Carol de; Noguchi, Henrique Kenich ; Toledo, Mônica Franco Zannini Junqueira ; Burrow, Robert A ; Pimenta, Daniel C. ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: AMINOÁCIDOS, PROTEÍNAS, AMIDAS
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ABNT
JESUS, Jéssica Carol de et al. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, v. 2022, n. 30, p. 1-7 art. e202200332, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200332. Acesso em: 06 jun. 2024.
APA
Jesus, J. C. de, Noguchi, H. K., Toledo, M. F. Z. J., Burrow, R. A., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, 2022( 30), 1-7 art. e202200332. doi:10.1002/ejoc.202200332
NLM
Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202200332
Vancouver
Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202200332
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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1002/ejoc.202200377
Artigo de periodico
Reactivity and Applications of Iodine Monochloride in Synthetic Approaches (2021)
Day, David P.; Alsenani, Nawaf I.; Alsimaree, Abdulrahman A.
Source: European Journal of Organic Chemistry. Unidade: IQSC
Assunto: OXIDAÇÃO
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ABNT
DAY, David P. e ALSENANI, Nawaf I. e ALSIMAREE, Abdulrahman A. Reactivity and Applications of Iodine Monochloride in Synthetic Approaches. European Journal of Organic Chemistry, v. 2021, n. 30, p. 4299 – 4307, 2021Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202100554. Acesso em: 06 jun. 2024.
APA
Day, D. P., Alsenani, N. I., & Alsimaree, A. A. (2021). Reactivity and Applications of Iodine Monochloride in Synthetic Approaches. European Journal of Organic Chemistry, 2021( 30), 4299 – 4307. doi:10.1002/ejoc.202100554
NLM
Day DP, Alsenani NI, Alsimaree AA. Reactivity and Applications of Iodine Monochloride in Synthetic Approaches [Internet]. European Journal of Organic Chemistry. 2021 ; 2021( 30): 4299 – 4307.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202100554
Vancouver
Day DP, Alsenani NI, Alsimaree AA. Reactivity and Applications of Iodine Monochloride in Synthetic Approaches [Internet]. European Journal of Organic Chemistry. 2021 ; 2021( 30): 4299 – 4307.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202100554
Artigo de periodico
Substituted Naphthols: Preparations, Applications, and Reactions (2021)
Vargas,Jorge Andrés Mora; Day, David P; Burtoloso, Antonio Carlos Bender
Source: European Journal of Organic Chemistry. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS
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ABNT
VARGAS, Jorge Andrés Mora e DAY, David P e BURTOLOSO, Antonio Carlos Bender. Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, v. press, 2021Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202001132. Acesso em: 06 jun. 2024.
APA
Vargas, J. A. M., Day, D. P., & Burtoloso, A. C. B. (2021). Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, press. doi:10.1002/ejoc.202001132
NLM
Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202001132
Vancouver
Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202001132
Artigo de periodico
Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones (2020)
Santos, Thiago dos ; Grundke, Caroline; Lucas, Tobias; Großmann, Luca; Clososki, Giuliano Cesar ; Opatz, Till
Source: European Journal of Organic Chemistry. Unidade: FCFRP
Subjects: QUÍMICA ORGÂNICA, BIOMASSA, CARBOIDRATOS, GLICOSE
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ABNT
SANTOS, Thiago dos et al. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, v. 2020, n. 41, p. 6429-6432, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000970. Acesso em: 06 jun. 2024.
APA
Santos, T. dos, Grundke, C., Lucas, T., Großmann, L., Clososki, G. C., & Opatz, T. (2020). Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, 2020( 41), 6429-6432. doi:10.1002/ejoc.202000970
NLM
Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000970
Vancouver
Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000970
Artigo de periodico
Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals (2020)
Paulino, Antonio Augusto Soares ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: UREIA, PALÁDIO, GLICOCONJUGADOS
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ABNT
PAULINO, Antonio Augusto Soares e STEFANI, Hélio Alexandre. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 3847–3855, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000494. Acesso em: 06 jun. 2024.
APA
Paulino, A. A. S., & Stefani, H. A. (2020). Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 3847–3855. doi:10.1002/ejoc.202000494
NLM
Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000494
Vancouver
Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000494
Artigo de periodico
α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals (2020)
Darbem, Mariana P; Esteves, Henrique A; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidades: FCF, IQ
Subjects: GLICOSÍDEOS, PALÁDIO
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ABNT
DARBEM, Mariana P et al. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 5220–5226, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000846. Acesso em: 06 jun. 2024.
APA
Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, & Stefani, H. A. (2020). α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 5220–5226. doi:10.1002/ejoc.202000846
NLM
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000846
Vancouver
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000846
Artigo de periodico
Multiple reversible dynamics of pyrimidine based acylhydrazones (2020)
Arango, Alejandra M.; Wist, Julien; Ellena, Javier ; D'Vries, Richard F.; Chaur, Manuel N.
Source: European Journal of Organic Chemistry. Unidade: IFSC
Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, ISÔMERO, NANOTECNOLOGIA
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ABNT
ARANGO, Alejandra M. et al. Multiple reversible dynamics of pyrimidine based acylhydrazones. European Journal of Organic Chemistry, v. 2020, n. 26, p. 4009-4017, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000553. Acesso em: 06 jun. 2024.
APA
Arango, A. M., Wist, J., Ellena, J., D'Vries, R. F., & Chaur, M. N. (2020). Multiple reversible dynamics of pyrimidine based acylhydrazones. European Journal of Organic Chemistry, 2020( 26), 4009-4017. doi:10.1002/ejoc.202000553
NLM
Arango AM, Wist J, Ellena J, D'Vries RF, Chaur MN. Multiple reversible dynamics of pyrimidine based acylhydrazones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 26): 4009-4017.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000553
Vancouver
Arango AM, Wist J, Ellena J, D'Vries RF, Chaur MN. Multiple reversible dynamics of pyrimidine based acylhydrazones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 26): 4009-4017.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000553
Artigo de periodico
Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones (2020)
Santos, Thiago dos ; Grundke, Caroline; Lucas, Tobias; Großmann, Luca; Clososki, Giuliano Cesar ; Opatz, Till
Source: European Journal of Organic Chemistry. Unidade: FCFRP
Subjects: GLICOSE, BIOMASSA, CARBOIDRATOS, PRODUTOS NATURAIS, SUSTENTABILIDADE
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ABNT
SANTOS, Thiago dos et al. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, v. 2020, n. 41, p. 6429-6432, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000970. Acesso em: 06 jun. 2024.
APA
Santos, T. dos, Grundke, C., Lucas, T., Großmann, L., Clososki, G. C., & Opatz, T. (2020). Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, 2020( 41), 6429-6432. doi:10.1002/ejoc.202000970
NLM
Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000970
Vancouver
Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.202000970
Artigo de periodico
The intermediates in lewis acid catalysis with lanthanide triflates (2019)
Tripodi, Guilherme L; Correra, Thiago Carita ; Angolini, Célio Fernando Figueiredo; Ferreira, Bruno Ricardo Viachã; Maître, Philippe; Eberlin, Marcos Nogueira; Roithová, Jana
Source: European Journal of Organic Chemistry. Unidade: IQ
Subjects: CATÁLISE, LANTANÍDIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TRIPODI, Guilherme L et al. The intermediates in lewis acid catalysis with lanthanide triflates. European Journal of Organic Chemistry, v. 22, p. 3560-3566, 2019Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201900171. Acesso em: 06 jun. 2024.
APA
Tripodi, G. L., Correra, T. C., Angolini, C. F. F., Ferreira, B. R. V., Maître, P., Eberlin, M. N., & Roithová, J. (2019). The intermediates in lewis acid catalysis with lanthanide triflates. European Journal of Organic Chemistry, 22, 3560-3566. doi:10.1002/ejoc.201900171
NLM
Tripodi GL, Correra TC, Angolini CFF, Ferreira BRV, Maître P, Eberlin MN, Roithová J. The intermediates in lewis acid catalysis with lanthanide triflates [Internet]. European Journal of Organic Chemistry. 2019 ; 22 3560-3566.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201900171
Vancouver
Tripodi GL, Correra TC, Angolini CFF, Ferreira BRV, Maître P, Eberlin MN, Roithová J. The intermediates in lewis acid catalysis with lanthanide triflates [Internet]. European Journal of Organic Chemistry. 2019 ; 22 3560-3566.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201900171
Artigo de periodico
Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides (2019)
Esteves, Henrique A; Darbem, Mariana P; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidades: BIOTECNOLOGIA, FCF
Subjects: MONÓXIDO DE CARBONO, PALÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESTEVES, Henrique A et al. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, v. 2019, p. 7384-7388, 2019Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201901081. Acesso em: 06 jun. 2024.
APA
Esteves, H. A., Darbem, M. P., Pimenta, D. C., & Stefani, H. A. (2019). Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, 2019, 7384-7388. doi:10.1002/ejoc.201901081
NLM
Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201901081
Vancouver
Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201901081
Artigo de periodico
C-H activation/metalation approaches for the synthesis of indolizine derivatives (2019)
Bertallo, Camila Rodrigues de Souza ; Arroio, Thais Rodrigues ; Toledo, Mônica Franco Zannini Junqueira; Sadler, Scott A.; Vessecchi, Ricardo ; Steel, Patrick G.; Clososki, Giuliano Cesar
Source: European Journal of Organic Chemistry. Unidades: FCF, FFCLRP, FCFRP
Subjects: COMPOSTOS ORGÂNICOS, AROMATIZANTES, SÍNTESE QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTALLO, Camila Rodrigues de Souza et al. C-H activation/metalation approaches for the synthesis of indolizine derivatives. European Journal of Organic Chemistry, v. 2019, n. 31-32, p. 5205-5213, 2019Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201900608. Acesso em: 06 jun. 2024.
APA
Bertallo, C. R. de S., Arroio, T. R., Toledo, M. F. Z. J., Sadler, S. A., Vessecchi, R., Steel, P. G., & Clososki, G. C. (2019). C-H activation/metalation approaches for the synthesis of indolizine derivatives. European Journal of Organic Chemistry, 2019( 31-32), 5205-5213. doi:10.1002/ejoc.201900608
NLM
Bertallo CR de S, Arroio TR, Toledo MFZJ, Sadler SA, Vessecchi R, Steel PG, Clososki GC. C-H activation/metalation approaches for the synthesis of indolizine derivatives [Internet]. European Journal of Organic Chemistry. 2019 ; 2019( 31-32): 5205-5213.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201900608
Vancouver
Bertallo CR de S, Arroio TR, Toledo MFZJ, Sadler SA, Vessecchi R, Steel PG, Clososki GC. C-H activation/metalation approaches for the synthesis of indolizine derivatives [Internet]. European Journal of Organic Chemistry. 2019 ; 2019( 31-32): 5205-5213.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201900608
Artigo de periodico
Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate (2018)
Santos, Camila S; Burtoloso, Antonio Carlos Bender
Source: European Journal of Organic Chemistry. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Camila S e BURTOLOSO, Antonio Carlos Bender. Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate. European Journal of Organic Chemistry, v. 2018, n. 45, 2018Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201801197. Acesso em: 06 jun. 2024.
APA
Santos, C. S., & Burtoloso, A. C. B. (2018). Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate. European Journal of Organic Chemistry, 2018( 45). doi:10.1002/ejoc.201801197
NLM
Santos CS, Burtoloso ACB. Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 45):[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201801197
Vancouver
Santos CS, Burtoloso ACB. Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 45):[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201801197
Artigo de periodico
Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones (2018)
Santiago, João Victor; Burtoloso, Antonio Carlos Bender
Source: European Journal of Organic Chemistry. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTIAGO, João Victor e BURTOLOSO, Antonio Carlos Bender. Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones. European Journal of Organic Chemistry, v. 2018, n. 22, p. 2822–2830, 2018Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201800239. Acesso em: 06 jun. 2024.
APA
Santiago, J. V., & Burtoloso, A. C. B. (2018). Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones. European Journal of Organic Chemistry, 2018( 22), 2822–2830. doi:10.1002/ejoc.201800239
NLM
Santiago JV, Burtoloso ACB. Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 22): 2822–2830.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201800239
Vancouver
Santiago JV, Burtoloso ACB. Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 22): 2822–2830.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201800239
Artigo de periodico
Bisarylselanylbenzo-2,1,3-selenadiazoles: synthesis, photophysical, electrochemical and singlet-oxygen-generation properties (2018)
Balaguez, Renata A; Kruger, Roberta; Iepsen, Bruna; Schumacher, Ricardo F; Oliboni, Robson S; Barcellos, Thiago; Junqueira, Helena Couto; Baptista, Maurício da Silva ; Iglesias, Bernardo A; Alves, Diego
Source: European Journal of Organic Chemistry. Unidade: IQ
Subjects: TERAPIA FOTODINÂMICA, ELETROQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BALAGUEZ, Renata A et al. Bisarylselanylbenzo-2,1,3-selenadiazoles: synthesis, photophysical, electrochemical and singlet-oxygen-generation properties. European Journal of Organic Chemistry, v. 46, p. 6507-6514, 2018Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201801186. Acesso em: 06 jun. 2024.
APA
Balaguez, R. A., Kruger, R., Iepsen, B., Schumacher, R. F., Oliboni, R. S., Barcellos, T., et al. (2018). Bisarylselanylbenzo-2,1,3-selenadiazoles: synthesis, photophysical, electrochemical and singlet-oxygen-generation properties. European Journal of Organic Chemistry, 46, 6507-6514. doi:10.1002/ejoc.201801186
NLM
Balaguez RA, Kruger R, Iepsen B, Schumacher RF, Oliboni RS, Barcellos T, Junqueira HC, Baptista M da S, Iglesias BA, Alves D. Bisarylselanylbenzo-2,1,3-selenadiazoles: synthesis, photophysical, electrochemical and singlet-oxygen-generation properties [Internet]. European Journal of Organic Chemistry. 2018 ; 46 6507-6514.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201801186
Vancouver
Balaguez RA, Kruger R, Iepsen B, Schumacher RF, Oliboni RS, Barcellos T, Junqueira HC, Baptista M da S, Iglesias BA, Alves D. Bisarylselanylbenzo-2,1,3-selenadiazoles: synthesis, photophysical, electrochemical and singlet-oxygen-generation properties [Internet]. European Journal of Organic Chemistry. 2018 ; 46 6507-6514.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ejoc.201801186

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