ReP USP - Resultado da busca

Artigo de periodico
Visible-Light-Mediated Strategies to Assemble Alkyl 2-Carboxylate-2,3,3-Trisubstituted β-Lactams and 5-Alkoxy-2,2,4-Trisubstituted Furan-3(2H)-ones Using Aryldiazoacetates and Aryldiazoketones (2021)
Munaretto, Laieli S; Santos, Caio Y. dos; Gallo, Rafael D. C; Okada Junior, Celso Yassuo; Deflon, Victor Marcelo ; Jurberg, Igor D
Source: Organic letters. Unidade: IQSC
Subjects: LUZ, FOTOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MUNARETTO, Laieli S et al. Visible-Light-Mediated Strategies to Assemble Alkyl 2-Carboxylate-2,3,3-Trisubstituted β-Lactams and 5-Alkoxy-2,2,4-Trisubstituted Furan-3(2H)-ones Using Aryldiazoacetates and Aryldiazoketones. Organic letters, v. 23, n. 23, p. 9292–9296, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c03662. Acesso em: 06 nov. 2024.
APA
Munaretto, L. S., Santos, C. Y. dos, Gallo, R. D. C., Okada Junior, C. Y., Deflon, V. M., & Jurberg, I. D. (2021). Visible-Light-Mediated Strategies to Assemble Alkyl 2-Carboxylate-2,3,3-Trisubstituted β-Lactams and 5-Alkoxy-2,2,4-Trisubstituted Furan-3(2H)-ones Using Aryldiazoacetates and Aryldiazoketones. Organic letters, 23( 23), 9292–9296. doi:10.1021/acs.orglett.1c03662
NLM
Munaretto LS, Santos CY dos, Gallo RDC, Okada Junior CY, Deflon VM, Jurberg ID. Visible-Light-Mediated Strategies to Assemble Alkyl 2-Carboxylate-2,3,3-Trisubstituted β-Lactams and 5-Alkoxy-2,2,4-Trisubstituted Furan-3(2H)-ones Using Aryldiazoacetates and Aryldiazoketones [Internet]. Organic letters. 2021 ; 23( 23): 9292–9296.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.1c03662
Vancouver
Munaretto LS, Santos CY dos, Gallo RDC, Okada Junior CY, Deflon VM, Jurberg ID. Visible-Light-Mediated Strategies to Assemble Alkyl 2-Carboxylate-2,3,3-Trisubstituted β-Lactams and 5-Alkoxy-2,2,4-Trisubstituted Furan-3(2H)-ones Using Aryldiazoacetates and Aryldiazoketones [Internet]. Organic letters. 2021 ; 23( 23): 9292–9296.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.1c03662
Artigo de periodico
A Selective C–C Bond Cleavage Strategy Promoted by Visible Light (2021)
Gallo, Rafael D. C; Duarte, Marcelo; Silva, Amanda F. da; Okada Junior, Celso Yassuo; Deflon, Victor Marcelo
Source: Organic letters. Unidade: IQSC
Assunto: LUZ
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GALLO, Rafael D. C et al. A Selective C–C Bond Cleavage Strategy Promoted by Visible Light. Organic letters, v. 23, n. 22, p. 8916–8920, 2021Tradução . . Disponível em: https://doi-org.ez67.periodicos.capes.gov.br/10.1021/acs.orglett.1c03406. Acesso em: 06 nov. 2024.
APA
Gallo, R. D. C., Duarte, M., Silva, A. F. da, Okada Junior, C. Y., & Deflon, V. M. (2021). A Selective C–C Bond Cleavage Strategy Promoted by Visible Light. Organic letters, 23( 22), 8916–8920. doi:10.1021/acs.orglett.1c03406
NLM
Gallo RDC, Duarte M, Silva AF da, Okada Junior CY, Deflon VM. A Selective C–C Bond Cleavage Strategy Promoted by Visible Light [Internet]. Organic letters. 2021 ; 23( 22): 8916–8920.[citado 2024 nov. 06 ] Available from: https://doi-org.ez67.periodicos.capes.gov.br/10.1021/acs.orglett.1c03406
Vancouver
Gallo RDC, Duarte M, Silva AF da, Okada Junior CY, Deflon VM. A Selective C–C Bond Cleavage Strategy Promoted by Visible Light [Internet]. Organic letters. 2021 ; 23( 22): 8916–8920.[citado 2024 nov. 06 ] Available from: https://doi-org.ez67.periodicos.capes.gov.br/10.1021/acs.orglett.1c03406
Artigo de periodico
Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids (2020)
Gallo, Rafael D. C; Momo, Patrícia B; Day, David P; Burtoloso, Antonio Carlos Bender
Source: Organic letters. Unidade: IQSC
Assunto: CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GALLO, Rafael D. C et al. Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids. Organic letters, v. 22, n. 6, p. 2339-2343 March 5, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.0c00540. Acesso em: 06 nov. 2024.
APA
Gallo, R. D. C., Momo, P. B., Day, D. P., & Burtoloso, A. C. B. (2020). Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids. Organic letters, 22( 6), 2339-2343 March 5. doi:10.1021/acs.orglett.0c00540
NLM
Gallo RDC, Momo PB, Day DP, Burtoloso ACB. Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids [Internet]. Organic letters. 2020 ; 22( 6): 2339-2343 March 5.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.0c00540
Vancouver
Gallo RDC, Momo PB, Day DP, Burtoloso ACB. Catalytic Friedel–Crafts Alkylation of Electron Rich Aromatic Derivatives with α-Aryl Diazoacetates Mediated by Brønsted Acids [Internet]. Organic letters. 2020 ; 22( 6): 2339-2343 March 5.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.0c00540
Artigo de periodico
Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides (2019)
Ahmad, Anees; Burtoloso, Antonio Carlos Bender
Source: Organic letters. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AHMAD, Anees e BURTOLOSO, Antonio Carlos Bender. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, v. 21, p. 6079-6083, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.9b02221. Acesso em: 06 nov. 2024.
APA
Ahmad, A., & Burtoloso, A. C. B. (2019). Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, 21, 6079-6083. doi:10.1021/acs.orglett.9b02221
NLM
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
Vancouver
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
Artigo de periodico
Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones (2018)
Talero, Alexánder G; Martins, Bruna S; Burtoloso, Antonio Carlos Bender
Source: Organic letters. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TALERO, Alexánder G e MARTINS, Bruna S e BURTOLOSO, Antonio Carlos Bender. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones. Organic letters, v. 20, p. 7206-7211, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.8b03126. Acesso em: 06 nov. 2024.
APA
Talero, A. G., Martins, B. S., & Burtoloso, A. C. B. (2018). Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones. Organic letters, 20, 7206-7211. doi:10.1021/acs.orglett.8b03126
NLM
Talero AG, Martins BS, Burtoloso ACB. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones [Internet]. Organic letters. 2018 ;20 7206-7211.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.8b03126
Vancouver
Talero AG, Martins BS, Burtoloso ACB. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones [Internet]. Organic letters. 2018 ;20 7206-7211.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.8b03126
Artigo de periodico
Catalyst - free insertion of sulfoxonium Ylides into Aryl Thiols: a direct preparation of beta-keto thioethers (2016)
Dias, Rafael Mafra de Paula; Burtoloso, Antonio Carlos Bender
Source: Organic letters. Unidade: IQSC
Assunto: CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DIAS, Rafael Mafra de Paula e BURTOLOSO, Antonio Carlos Bender. Catalyst - free insertion of sulfoxonium Ylides into Aryl Thiols: a direct preparation of beta-keto thioethers. Organic letters, v. 18, n. 12, p. 3034-3037, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.6b01470. Acesso em: 06 nov. 2024.
APA
Dias, R. M. de P., & Burtoloso, A. C. B. (2016). Catalyst - free insertion of sulfoxonium Ylides into Aryl Thiols: a direct preparation of beta-keto thioethers. Organic letters, 18( 12), 3034-3037. doi:10.1021/acs.orglett.6b01470
NLM
Dias RM de P, Burtoloso ACB. Catalyst - free insertion of sulfoxonium Ylides into Aryl Thiols: a direct preparation of beta-keto thioethers [Internet]. Organic letters. 2016 ; 18( 12): 3034-3037.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.6b01470
Vancouver
Dias RM de P, Burtoloso ACB. Catalyst - free insertion of sulfoxonium Ylides into Aryl Thiols: a direct preparation of beta-keto thioethers [Internet]. Organic letters. 2016 ; 18( 12): 3034-3037.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.orglett.6b01470

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Funding Agencies