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Artigo de periodico
Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones (2022)
Momo, Patrícia Betoni ; Mizobuchi,Eduardo F; Echemendía, Radell ; Baddeley, Isabel; Grayson, Matthew N. ; Burtoloso, Antonio Carlos Bender
Source: The Journal of Organic Chemistry. Unidade: IQSC
Subjects: LIPÍDEOS, CROMATOGRAFIA LÍQUIDA, CATÁLISE
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ABNT
MOMO, Patrícia Betoni et al. Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones. The Journal of Organic Chemistry, v. 87, p. 3482−3490, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.1c03045. Acesso em: 16 nov. 2024.
APA
Momo, P. B., Mizobuchi, E. F., Echemendía, R., Baddeley, I., Grayson, M. N., & Burtoloso, A. C. B. (2022). Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones. The Journal of Organic Chemistry, 87, 3482−3490. doi:10.1021/acs.joc.1c03045
NLM
Momo PB, Mizobuchi EF, Echemendía R, Baddeley I, Grayson MN, Burtoloso ACB. Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones [Internet]. The Journal of Organic Chemistry. 2022 ; 87 3482−3490.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1021/acs.joc.1c03045
Vancouver
Momo PB, Mizobuchi EF, Echemendía R, Baddeley I, Grayson MN, Burtoloso ACB. Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones [Internet]. The Journal of Organic Chemistry. 2022 ; 87 3482−3490.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1021/acs.joc.1c03045
Artigo de periodico
Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides (2020)
Momo, Patrícia Betoni ; Leveille, Alexandria N. ; Farrar, Elliot H. E. ; Grayson, Matthew N. ; Mattson, Anita E.; Burtoloso, Antonio Carlos Bender
Source: Angewandte Chemie International Edition. Unidade: IQSC
Subjects: CATÁLISE, REAGENTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOMO, Patrícia Betoni et al. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides. Angewandte Chemie International Edition, v. 59, p. 15554–15559 , 2020Tradução . . Disponível em: https://doi.org/10.1002/anie.202005563. Acesso em: 16 nov. 2024.
APA
Momo, P. B., Leveille, A. N., Farrar, E. H. E., Grayson, M. N., Mattson, A. E., & Burtoloso, A. C. B. (2020). Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides. Angewandte Chemie International Edition, 59, 15554–15559 . doi:10.1002/anie.202005563
NLM
Momo PB, Leveille AN, Farrar EHE, Grayson MN, Mattson AE, Burtoloso ACB. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides [Internet]. Angewandte Chemie International Edition. 2020 ; 59 15554–15559 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/anie.202005563
Vancouver
Momo PB, Leveille AN, Farrar EHE, Grayson MN, Mattson AE, Burtoloso ACB. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides [Internet]. Angewandte Chemie International Edition. 2020 ; 59 15554–15559 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/anie.202005563
Artigo de periodico
Metal-free Insertion Reactions of Diazo carbonyls to Azlactones (2018)
Mello,Amanda C.; Momo, Patrícia Betoni; Burtoloso, Antonio Carlos Bender ; Amarante, Giovanni W
Source: The Journal of Organic Chemistry. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELLO, Amanda C. et al. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones. The Journal of Organic Chemistry, v. 83, p. 11399-11406, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.8b01683. Acesso em: 16 nov. 2024.
APA
Mello, A. C., Momo, P. B., Burtoloso, A. C. B., & Amarante, G. W. (2018). Metal-free Insertion Reactions of Diazo carbonyls to Azlactones. The Journal of Organic Chemistry, 83, 11399-11406. doi:10.1021/acs.joc.8b01683
NLM
Mello AC, Momo PB, Burtoloso ACB, Amarante GW. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones [Internet]. The Journal of Organic Chemistry. 2018 ;83 11399-11406.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1021/acs.joc.8b01683
Vancouver
Mello AC, Momo PB, Burtoloso ACB, Amarante GW. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones [Internet]. The Journal of Organic Chemistry. 2018 ;83 11399-11406.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1021/acs.joc.8b01683
Trabalho de evento-resumo
One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin (2017)
Momo, Patrícia Betoni; Dias, Rafael Mafra de Paula; Burtoloso, Antonio Carlos Bender
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOMO, Patrícia Betoni e DIAS, Rafael Mafra de Paula e BURTOLOSO, Antonio Carlos Bender. One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf. Acesso em: 16 nov. 2024.
APA
Momo, P. B., Dias, R. M. de P., & Burtoloso, A. C. B. (2017). One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf
NLM
Momo PB, Dias RM de P, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin [Internet]. Proceedings. 2017 ;[citado 2024 nov. 16 ] Available from: https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf
Vancouver
Momo PB, Dias RM de P, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3-pyrrolidinones from alfa,beta-insatured diazoketones and amines: application in the synthesis of barmumycin [Internet]. Proceedings. 2017 ;[citado 2024 nov. 16 ] Available from: https://repositorio.usp.br/directbitstream/779bbe53-eb5e-4f2a-9286-bebc55c0aa53/P16978.pdf
Artigo de periodico
One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin (2017)
Dias, Rafael Mafra de Paula; Momo, Patrícia Betoni; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DIAS, Rafael Mafra de Paula e MOMO, Patrícia Betoni e BURTOLOSO, Antonio Carlos Bender. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, v. 73, n. 26, p. 3720 - 3729, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2017.05.040. Acesso em: 16 nov. 2024.
APA
Dias, R. M. de P., Momo, P. B., & Burtoloso, A. C. B. (2017). One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, 73( 26), 3720 - 3729. doi:10.1016/j.tet.2017.05.040
NLM
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040
Vancouver
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040

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