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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: 24 ago. 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 ago. 24 ] 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 ago. 24 ] Available from: https://dx.doi.org/10.1002/ejoc.202300930
Artigo de periodico
Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones (2021)
Day, David P; Vargas, Jorge A. M.; Burtoloso, Antonio Carlos Bender
Source: The Chemical Record. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
DAY, David P e VARGAS, Jorge A. M. e BURTOLOSO, Antonio Carlos Bender. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, v. 21, p. 1-19, 2021Tradução . . Disponível em: https://doi.org/10.1002/tcr.20200017. Acesso em: 24 ago. 2024.
APA
Day, D. P., Vargas, J. A. M., & Burtoloso, A. C. B. (2021). Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, 21, 1-19. doi:10.1002/tcr.20200017
NLM
Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/tcr.20200017
Vancouver
Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/tcr.20200017
Artigo de periodico
Flow synthesis of 2-[methyl(pyridin-2-yl)amino]ethanol: an experimental and computational study (2021)
Calvo, Paulo Victor Cuesta ; Batista, Patrick Rodrigues ; Silva, Renan Rodrigues de Oliveira; Arni, Saleh Al ; Solisio, Carlo; Ducati, Lucas Colucci ; Palma, Mauri Sérgio Alves
Source: Chemical Engineering Technology. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, MEDICAMENTO, TERMODINÂMICA QUÍMICA
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ABNT
CALVO, Paulo Victor Cuesta et al. Flow synthesis of 2-[methyl(pyridin-2-yl)amino]ethanol: an experimental and computational study. Chemical Engineering Technology, v. 44, n. 2, p. 283–290, 2021Tradução . . Disponível em: https://doi.org/10.1002/ceat.202000423. Acesso em: 24 ago. 2024.
APA
Calvo, P. V. C., Batista, P. R., Silva, R. R. de O., Arni, S. A., Solisio, C., Ducati, L. C., & Palma, M. S. A. (2021). Flow synthesis of 2-[methyl(pyridin-2-yl)amino]ethanol: an experimental and computational study. Chemical Engineering Technology, 44( 2), 283–290. doi:10.1002/ceat.202000423
NLM
Calvo PVC, Batista PR, Silva RR de O, Arni SA, Solisio C, Ducati LC, Palma MSA. Flow synthesis of 2-[methyl(pyridin-2-yl)amino]ethanol: an experimental and computational study [Internet]. Chemical Engineering Technology. 2021 ; 44( 2): 283–290.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ceat.202000423
Vancouver
Calvo PVC, Batista PR, Silva RR de O, Arni SA, Solisio C, Ducati LC, Palma MSA. Flow synthesis of 2-[methyl(pyridin-2-yl)amino]ethanol: an experimental and computational study [Internet]. Chemical Engineering Technology. 2021 ; 44( 2): 283–290.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ceat.202000423
Artigo de periodico
Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations (2020)
Nishimura, Rodolfo Hideki Vicente ; Murie, Valter Eduardo ; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Source: ChemistrySelect. Unidades: FFCLRP, FCFRP
Subjects: METALIZAÇÃO, COMPOSTOS ORGANOMETÁLICOS, QUÍMICA MÉDICA, SÍNTESE ORGÂNICA, AMIDAS
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ABNT
NISHIMURA, Rodolfo Hideki Vicente et al. Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations. ChemistrySelect, v. 5, n. 36, p. 11106-11111, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202002589. Acesso em: 24 ago. 2024.
APA
Nishimura, R. H. V., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2020). Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations. ChemistrySelect, 5( 36), 11106-11111. doi:10.1002/slct.202002589
NLM
Nishimura RHV, Murie VE, Vessecchi R, Clososki GC. Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations [Internet]. ChemistrySelect. 2020 ; 5( 36): 11106-11111.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/slct.202002589
Vancouver
Nishimura RHV, Murie VE, Vessecchi R, Clososki GC. Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations [Internet]. ChemistrySelect. 2020 ; 5( 36): 11106-11111.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/slct.202002589
Artigo de periodico
Syntheses and Applications of Malonamide Derivatives – A Minireview (2020)
Aderibigbe, Abiodun D.; Day, David P
Source: ChemistrySelect. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
ADERIBIGBE, Abiodun D. e DAY, David P. Syntheses and Applications of Malonamide Derivatives – A Minireview. ChemistrySelect, v. 5, p. 15222–15232, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202004340. Acesso em: 24 ago. 2024.
APA
Aderibigbe, A. D., & Day, D. P. (2020). Syntheses and Applications of Malonamide Derivatives – A Minireview. ChemistrySelect, 5, 15222–15232. doi:10.1002/slct.202004340
NLM
Aderibigbe AD, Day DP. Syntheses and Applications of Malonamide Derivatives – A Minireview [Internet]. ChemistrySelect. 2020 ; 5 15222–15232.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/slct.202004340
Vancouver
Aderibigbe AD, Day DP. Syntheses and Applications of Malonamide Derivatives – A Minireview [Internet]. ChemistrySelect. 2020 ; 5 15222–15232.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/slct.202004340
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
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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: 24 ago. 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 ago. 24 ] 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 ago. 24 ] 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
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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: 24 ago. 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 ago. 24 ] 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 ago. 24 ] Available from: https://doi.org/10.1002/ejoc.201800239
Artigo de periodico
Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Synthesis. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 24 ago. 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
NLM
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0036-1589090
Vancouver
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0036-1589090
Artigo de periodico
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
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ABNT
VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 24 ago. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ajoc.201700154
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ajoc.201700154
Artigo de periodico
Lipid Matrices destabilization induced by some newly synthesized pyridinium salts (2017)
Luchese, Angelica M; Di Vitta, Cláudio ; Marzorati, Liliana ; Yamaoka , Patrícia; Funari, Sérgio S
Source: ChemistrySelect. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
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ABNT
LUCHESE, Angelica M et al. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts. ChemistrySelect, v. 2, n. 4, p. 1491-1496, 2017Tradução . . Disponível em: https://doi.org/10.1002/slct.201601588. Acesso em: 24 ago. 2024.
APA
Luchese, A. M., Di Vitta, C., Marzorati, L., Yamaoka , P., & Funari, S. S. (2017). Lipid Matrices destabilization induced by some newly synthesized pyridinium salts. ChemistrySelect, 2( 4), 1491-1496. doi:10.1002/slct.201601588
NLM
Luchese AM, Di Vitta C, Marzorati L, Yamaoka P, Funari SS. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts [Internet]. ChemistrySelect. 2017 ; 2( 4): 1491-1496.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/slct.201601588
Vancouver
Luchese AM, Di Vitta C, Marzorati L, Yamaoka P, Funari SS. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts [Internet]. ChemistrySelect. 2017 ; 2( 4): 1491-1496.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/slct.201601588
Parte de monografia/livro
Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*) (2016)
Santos, Marilia Silva; Correia, José Tiago Menezes; Batista, Ana Paula de Lima; Rodrigues Junior, Manoel Trindade; Braga, Ataualpa Albert Carmo ; Eberlin, Marcos Nogueira; Coelho, Fernando
Source: Lewis base catalysis in organic synthesis. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
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ABNT
SANTOS, Marilia Silva et al. Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*). Lewis base catalysis in organic synthesis. Tradução . Weinheim: Wiley-VCH Verlag, 2016. . Disponível em: https://doi.org/10.1002/9783527675142.ch7. Acesso em: 24 ago. 2024.
APA
Santos, M. S., Correia, J. T. M., Batista, A. P. de L., Rodrigues Junior, M. T., Braga, A. A. C., Eberlin, M. N., & Coelho, F. (2016). Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*). In Lewis base catalysis in organic synthesis. Weinheim: Wiley-VCH Verlag. doi:10.1002/9783527675142.ch7
NLM
Santos MS, Correia JTM, Batista AP de L, Rodrigues Junior MT, Braga AAC, Eberlin MN, Coelho F. Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*) [Internet]. In: Lewis base catalysis in organic synthesis. Weinheim: Wiley-VCH Verlag; 2016. [citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/9783527675142.ch7
Vancouver
Santos MS, Correia JTM, Batista AP de L, Rodrigues Junior MT, Braga AAC, Eberlin MN, Coelho F. Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*) [Internet]. In: Lewis base catalysis in organic synthesis. Weinheim: Wiley-VCH Verlag; 2016. [citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/9783527675142.ch7
Artigo de periodico
Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds (2016)
Bernardim, Barbara; Couch, Erica D.; Hardman-Baldwin, Andrea M; Burtoloso, Antonio Carlos Bender ; Mattson, Anitta E
Source: Synthesis. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, UREIA
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ABNT
BERNARDIM, Barbara et al. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, v. 48, n. 5, p. 677-686, 2016Tradução . . Disponível em: https://doi.org/10.1055/s-0035-1561061. Acesso em: 24 ago. 2024.
APA
Bernardim, B., Couch, E. D., Hardman-Baldwin, A. M., Burtoloso, A. C. B., & Mattson, A. E. (2016). Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, 48( 5), 677-686. doi:10.1055/s-0035-1561061
NLM
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0035-1561061
Vancouver
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0035-1561061
Artigo de periodico
DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction (2016)
Batista, Ana Paula de Lima; Coelho, Fernando; Braga, Ataualpa Albert Carmo
Source: Theoretical Chemistry Accounts. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, CATÁLISE
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ABNT
BATISTA, Ana Paula de Lima e COELHO, Fernando e BRAGA, Ataualpa Albert Carmo. DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction. Theoretical Chemistry Accounts, v. 135, p. 1-8 art. 186, 2016Tradução . . Disponível em: https://doi.org/10.1007/s00214-016-1946-1. Acesso em: 24 ago. 2024.
APA
Batista, A. P. de L., Coelho, F., & Braga, A. A. C. (2016). DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction. Theoretical Chemistry Accounts, 135, 1-8 art. 186. doi:10.1007/s00214-016-1946-1
NLM
Batista AP de L, Coelho F, Braga AAC. DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction [Internet]. Theoretical Chemistry Accounts. 2016 ; 135 1-8 art. 186.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s00214-016-1946-1
Vancouver
Batista AP de L, Coelho F, Braga AAC. DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction [Internet]. Theoretical Chemistry Accounts. 2016 ; 135 1-8 art. 186.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s00214-016-1946-1
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
Source: European Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP
Subjects: 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: 24 ago. 2024.
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 2024 ago. 24 ] 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 2024 ago. 24 ] Available from: https://doi.org/10.1002/ejoc.201403255
Artigo de periodico
The (5Z)-5-pentacosenoics and 6-pentacosynoic acis inibit the HIV-1 reverse transcriptase (2015)
Moreira, Lizabeth Giménez; Orellano, Elsie A.; Rosado, Karolyna; Guido, Rafael Victorio Carvalho; Andricopulo, Adriano Defini; Soto, Gabriela Ortiz; Rodríguez, José W.; Sanabria-Ríos, David J.; Carballeira, Néstor M.
Source: Lipids. Unidade: IFSC
Subjects: HIV, ÁCIDOS GRAXOS, SÍNTESE ORGÂNICA
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ABNT
MOREIRA, Lizabeth Giménez et al. The (5Z)-5-pentacosenoics and 6-pentacosynoic acis inibit the HIV-1 reverse transcriptase. Lipids, v. 50, n. 10, p. 1043-1050 + supplementary material, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11745-015-4064-2. Acesso em: 24 ago. 2024.
APA
Moreira, L. G., Orellano, E. A., Rosado, K., Guido, R. V. C., Andricopulo, A. D., Soto, G. O., et al. (2015). The (5Z)-5-pentacosenoics and 6-pentacosynoic acis inibit the HIV-1 reverse transcriptase. Lipids, 50( 10), 1043-1050 + supplementary material. doi:10.1007/s11745-015-4064-2
NLM
Moreira LG, Orellano EA, Rosado K, Guido RVC, Andricopulo AD, Soto GO, Rodríguez JW, Sanabria-Ríos DJ, Carballeira NM. The (5Z)-5-pentacosenoics and 6-pentacosynoic acis inibit the HIV-1 reverse transcriptase [Internet]. Lipids. 2015 ; 50( 10): 1043-1050 + supplementary material.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s11745-015-4064-2
Vancouver
Moreira LG, Orellano EA, Rosado K, Guido RVC, Andricopulo AD, Soto GO, Rodríguez JW, Sanabria-Ríos DJ, Carballeira NM. The (5Z)-5-pentacosenoics and 6-pentacosynoic acis inibit the HIV-1 reverse transcriptase [Internet]. Lipids. 2015 ; 50( 10): 1043-1050 + supplementary material.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s11745-015-4064-2
Artigo de periodico
(Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins (2015)
Nishimura, Rodolfo H. V.; Murie, Valter E.; Soldi, Rafael A.; Clososki, Giuliano César
Source: Synthesis. Unidade: FCFRP
Subjects: ALDEÍDOS, CLORETO, COMPOSTOS ORGANOMETÁLICOS, REAGENTES, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NISHIMURA, Rodolfo H. V. et al. (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins. Synthesis, v. 47, n. 10, p. 1455-1460, 2015Tradução . . Disponível em: https://doi.org/10.1055/s-0034-1380288. Acesso em: 24 ago. 2024.
APA
Nishimura, R. H. V., Murie, V. E., Soldi, R. A., & Clososki, G. C. (2015). (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins. Synthesis, 47( 10), 1455-1460. doi:10.1055/s-0034-1380288
NLM
Nishimura RHV, Murie VE, Soldi RA, Clososki GC. (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins [Internet]. Synthesis. 2015 ; 47( 10): 1455-1460.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0034-1380288
Vancouver
Nishimura RHV, Murie VE, Soldi RA, Clososki GC. (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins [Internet]. Synthesis. 2015 ; 47( 10): 1455-1460.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0034-1380288
Artigo de periodico
Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters (2014)
Stefani, Hélio Alexandre ; Manarin, Flávia; Khan, Amna N; Vasconcelos, Stanley Nunes Siqueira
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: ITÉRBIO, BORO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, v. 6, p. 1236-1240, 2014Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201301421. Acesso em: 24 ago. 2024.
APA
Stefani, H. A., Manarin, F., Khan, A. N., & Vasconcelos, S. N. S. (2014). Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, 6, 1236-1240. doi:10.1002/ejoc.201301421
NLM
Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ejoc.201301421
Vancouver
Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ejoc.201301421
Artigo de periodico
Accdouvntentures in ring-contraction reactions (2014)
Silva Junior, Luiz Fernando da
Source: Synlett. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, TÁLIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JUNIOR, Luiz Fernando da. Accdouvntentures in ring-contraction reactions. Synlett, v. 25, p. 466-476, 2014Tradução . . Disponível em: https://doi.org/10.1055/s-0033-1340472. Acesso em: 24 ago. 2024.
APA
Silva Junior, L. F. da. (2014). Accdouvntentures in ring-contraction reactions. Synlett, 25, 466-476. doi:10.1055/s-0033-1340472
NLM
Silva Junior LF da. Accdouvntentures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25 466-476.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0033-1340472
Vancouver
Silva Junior LF da. Accdouvntentures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25 466-476.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0033-1340472
Artigo de periodico
Transformation of saturated nitrogen-containing heterocyclic compounds by microorganisms (2014)
Parshikov, Igor A.; Silva, Eliane O.; Furtado, Niege Araçari Jacometti Cardoso
Source: Applied Microbiology and Biotechnology. Unidade: FCFRP
Subjects: BIOTRANSFORMAÇÃO, COMPOSTOS HETEROCÍCLICOS, FARMACOLOGIA, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARSHIKOV, Igor A. e SILVA, Eliane O. e FURTADO, Niege Araçari Jacometti Cardoso. Transformation of saturated nitrogen-containing heterocyclic compounds by microorganisms. Applied Microbiology and Biotechnology, v. 98, n. 4, p. 1497-1506, 2014Tradução . . Disponível em: https://doi.org/10.1007/s00253-013-5429-1. Acesso em: 24 ago. 2024.
APA
Parshikov, I. A., Silva, E. O., & Furtado, N. A. J. C. (2014). Transformation of saturated nitrogen-containing heterocyclic compounds by microorganisms. Applied Microbiology and Biotechnology, 98( 4), 1497-1506. doi:10.1007/s00253-013-5429-1
NLM
Parshikov IA, Silva EO, Furtado NAJC. Transformation of saturated nitrogen-containing heterocyclic compounds by microorganisms [Internet]. Applied Microbiology and Biotechnology. 2014 ; 98( 4): 1497-1506.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s00253-013-5429-1
Vancouver
Parshikov IA, Silva EO, Furtado NAJC. Transformation of saturated nitrogen-containing heterocyclic compounds by microorganisms [Internet]. Applied Microbiology and Biotechnology. 2014 ; 98( 4): 1497-1506.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s00253-013-5429-1
Artigo de periodico
Adventures in ring-contraction reactions (2014)
Silva Junior, Luiz Fernando da
Source: Synlett. Unidade: IQ
Subjects: TÁLIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JUNIOR, Luiz Fernando da. Adventures in ring-contraction reactions. Synlett, v. 25, n. 4, p. 466-476, 2014Tradução . . Disponível em: https://doi.org/10.1055/s-0033-1340472. Acesso em: 24 ago. 2024.
APA
Silva Junior, L. F. da. (2014). Adventures in ring-contraction reactions. Synlett, 25( 4), 466-476. doi:10.1055/s-0033-1340472
NLM
Silva Junior LF da. Adventures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25( 4): 466-476.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0033-1340472
Vancouver
Silva Junior LF da. Adventures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25( 4): 466-476.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0033-1340472

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