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Artigo de periodico
Molecular iodine-mediated functionalization of α-carbonyl sulfoxonium ylides with thiocyanates, xanthates, and dithiocarbamates (2025)
Capellaro, Kauê C.; Burtoloso, Antonio Carlos Bender
Fonte: European Journal of Organic Chemistry. Unidade: IQSC
Assuntos: IODO, REAÇÕES QUÍMICAS, QUÍMICA ORGÂNICA
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ABNT
CAPELLARO, Kauê C. e BURTOLOSO, Antonio Carlos Bender. Molecular iodine-mediated functionalization of α-carbonyl sulfoxonium ylides with thiocyanates, xanthates, and dithiocarbamates. European Journal of Organic Chemistry, p. e202500518, 2025Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202500518. Acesso em: 07 dez. 2025.
APA
Capellaro, K. C., & Burtoloso, A. C. B. (2025). Molecular iodine-mediated functionalization of α-carbonyl sulfoxonium ylides with thiocyanates, xanthates, and dithiocarbamates. European Journal of Organic Chemistry, e202500518. doi:10.1002/ejoc.202500518
NLM
Capellaro KC, Burtoloso ACB. Molecular iodine-mediated functionalization of α-carbonyl sulfoxonium ylides with thiocyanates, xanthates, and dithiocarbamates [Internet]. European Journal of Organic Chemistry. 2025 ;e202500518.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.202500518
Vancouver
Capellaro KC, Burtoloso ACB. Molecular iodine-mediated functionalization of α-carbonyl sulfoxonium ylides with thiocyanates, xanthates, and dithiocarbamates [Internet]. European Journal of Organic Chemistry. 2025 ;e202500518.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.202500518
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
Fonte: European Journal of Organic Chemistry. Unidade: IQSC
Assuntos: 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: 07 dez. 2025.
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 2025 dez. 07 ] 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 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.202200441
Artigo de periodico
Substituted Naphthols: Preparations, Applications, and Reactions (2021)
Vargas,Jorge Andrés Mora; Day, David P; Burtoloso, Antonio Carlos Bender
Fonte: European Journal of Organic Chemistry. Unidade: IQSC
Assuntos: 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: 07 dez. 2025.
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 2025 dez. 07 ] 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 2025 dez. 07 ] 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
Fonte: European Journal of Organic Chemistry. Unidade: FCFRP
Assuntos: 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: 07 dez. 2025.
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 2025 dez. 07 ] 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 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.202000970
Artigo de periodico
Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl (2015)
Batista, João H. C.; Santos, Fernanda M. dos; Bozzini, Leandro A.; Vessecchi, Ricardo; Oliveira, Alfredo Ricardo Marques de; Clososki, Giuliano Cesar
Fonte: European Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP
Assuntos: QUÍMICA ORGÂNICA, MAGNÉSIO, SÍNTESE ORGÂNICA
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ABNT
BATISTA, João H. C. et al. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl. European Journal of Organic Chemistry, v. 2015, n. 5, p. 967-977, 2015Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201403255. Acesso em: 07 dez. 2025.
APA
Batista, J. H. C., Santos, F. M. dos, Bozzini, L. A., Vessecchi, R., Oliveira, A. R. M. de, & Clososki, G. C. (2015). Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl. European Journal of Organic Chemistry, 2015( 5), 967-977. doi:10.1002/ejoc.201403255
NLM
Batista JHC, Santos FM dos, Bozzini LA, Vessecchi R, Oliveira ARM de, Clososki GC. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl [Internet]. European Journal of Organic Chemistry. 2015 ; 2015( 5): 967-977.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.201403255
Vancouver
Batista JHC, Santos FM dos, Bozzini LA, Vessecchi R, Oliveira ARM de, Clososki GC. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl [Internet]. European Journal of Organic Chemistry. 2015 ; 2015( 5): 967-977.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.201403255
Artigo de periodico
Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions (2013)
Burtoloso, Antonio Carlos Bender ; Dias, Rafael M; Leonarczyk, Ives Antonio
Fonte: European Journal of Organic Chemistry. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
BURTOLOSO, Antonio Carlos Bender e DIAS, Rafael M e LEONARCZYK, Ives Antonio. Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions. European Journal of Organic Chemistry, n. 23, p. 5005-5016, 2013Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201300581. Acesso em: 07 dez. 2025.
APA
Burtoloso, A. C. B., Dias, R. M., & Leonarczyk, I. A. (2013). Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions. European Journal of Organic Chemistry, ( 23), 5005-5016. doi:10.1002/ejoc.201300581
NLM
Burtoloso ACB, Dias RM, Leonarczyk IA. Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions [Internet]. European Journal of Organic Chemistry. 2013 ;( 23): 5005-5016.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.201300581
Vancouver
Burtoloso ACB, Dias RM, Leonarczyk IA. Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions [Internet]. European Journal of Organic Chemistry. 2013 ;( 23): 5005-5016.[citado 2025 dez. 07 ] Available from: https://doi.org/10.1002/ejoc.201300581
Artigo de periodico
Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation? (2008)
Martins, Clarissa Tavares; Lima, Michelle de Souza; Bastos, Erick Leite ; El Seoud, Omar A
Fonte: European Journal of Organic Chemistry. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, SOLVENTE
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ABNT
MARTINS, Clarissa Tavares et al. Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation?. European Journal of Organic Chemistry, n. 7, p. 1165-1180, 2008Tradução . . Acesso em: 07 dez. 2025.
APA
Martins, C. T., Lima, M. de S., Bastos, E. L., & El Seoud, O. A. (2008). Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation? European Journal of Organic Chemistry, (7), 1165-1180.
NLM
Martins CT, Lima M de S, Bastos EL, El Seoud OA. Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation? European Journal of Organic Chemistry. 2008 ;(7): 1165-1180.[citado 2025 dez. 07 ]
Vancouver
Martins CT, Lima M de S, Bastos EL, El Seoud OA. Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation? European Journal of Organic Chemistry. 2008 ;(7): 1165-1180.[citado 2025 dez. 07 ]
Artigo de periodico
Studies on the mechanism of the excitation step in peroxyoxalate chemiluminescence (2000)
Stevani, Cassius Vinicius ; Silva, Sandra Maria da; Baader, Wilhelm Josef
Fonte: European Journal of Organic Chemistry. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, LUMINESCÊNCIA
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ABNT
STEVANI, Cassius Vinicius e SILVA, Sandra Maria da e BAADER, Wilhelm Josef. Studies on the mechanism of the excitation step in peroxyoxalate chemiluminescence. European Journal of Organic Chemistry, n. 24, p. 4037-4046, 2000Tradução . . Acesso em: 07 dez. 2025.
APA
Stevani, C. V., Silva, S. M. da, & Baader, W. J. (2000). Studies on the mechanism of the excitation step in peroxyoxalate chemiluminescence. European Journal of Organic Chemistry, ( 24), 4037-4046.
NLM
Stevani CV, Silva SM da, Baader WJ. Studies on the mechanism of the excitation step in peroxyoxalate chemiluminescence. European Journal of Organic Chemistry. 2000 ;( 24): 4037-4046.[citado 2025 dez. 07 ]
Vancouver
Stevani CV, Silva SM da, Baader WJ. Studies on the mechanism of the excitation step in peroxyoxalate chemiluminescence. European Journal of Organic Chemistry. 2000 ;( 24): 4037-4046.[citado 2025 dez. 07 ]

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