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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
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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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1002/anie.202005563
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
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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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1021/acs.orglett.0c00540
Artigo de periodico
Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling (2020)
Bernardim, Barbara ; Dunsmore, Lavinia ; Li, He; Hocking, Brad; Nuñez-Franco, Reyes; Navo, Claudio D. ; Jiménez-Osés, Gonzalo ; Burtoloso, Antonio Carlos Bender ; Bernardes, Gonçalo J. L.
Source: Bioconjugate Chemistry. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, REAGENTES, PROTEÍNAS, ANTICORPOS
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ABNT
BERNARDIM, Barbara et al. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling. Bioconjugate Chemistry, v. 31, n. 6, p. 1604-1610 June 2020, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.bioconjchem.0c00232. Acesso em: 09 jun. 2024.
APA
Bernardim, B., Dunsmore, L., Li, H., Hocking, B., Nuñez-Franco, R., Navo, C. D., et al. (2020). Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling. Bioconjugate Chemistry, 31( 6), 1604-1610 June 2020. doi:10.1021/acs.bioconjchem.0c00232
NLM
Bernardim B, Dunsmore L, Li H, Hocking B, Nuñez-Franco R, Navo CD, Jiménez-Osés G, Burtoloso ACB, Bernardes GJL. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling [Internet]. Bioconjugate Chemistry. 2020 ; 31( 6): 1604-1610 June 2020.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1021/acs.bioconjchem.0c00232
Vancouver
Bernardim B, Dunsmore L, Li H, Hocking B, Nuñez-Franco R, Navo CD, Jiménez-Osés G, Burtoloso ACB, Bernardes GJL. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling [Internet]. Bioconjugate Chemistry. 2020 ; 31( 6): 1604-1610 June 2020.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1021/acs.bioconjchem.0c00232
Artigo de periodico
α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles (2020)
Caiuby, Clarice Alves Dale ; Jesus, Matheus Pereira de ; Burtoloso, Antonio Carlos Bender
Source: The Journal of Organic Chemistry. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
CAIUBY, Clarice Alves Dale e JESUS, Matheus Pereira de e BURTOLOSO, Antonio Carlos Bender. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, v. 85, n. 11, p. 7433-7445 April 28, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.0c00833. Acesso em: 09 jun. 2024.
APA
Caiuby, C. A. D., Jesus, M. P. de, & Burtoloso, A. C. B. (2020). α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, 85( 11), 7433-7445 April 28. doi:10.1021/acs.joc.0c00833
NLM
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
Vancouver
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
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
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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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
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
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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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1021/acs.joc.8b01683
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
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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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1021/acs.orglett.8b03126
Artigo de periodico
Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds (2018)
Gallo, Rafael D. C; Burtoloso, Antonio Carlos Bender
Source: Green Chemistry. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
GALLO, Rafael D. C e BURTOLOSO, Antonio Carlos Bender. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, v. 20, p. 4547-4556, 2018Tradução . . Disponível em: https://doi.org/10.1039/C8GC02574F. Acesso em: 09 jun. 2024.
APA
Gallo, R. D. C., & Burtoloso, A. C. B. (2018). Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, 20, 4547-4556. doi:10.1039/C8GC02574F
NLM
Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1039/C8GC02574F
Vancouver
Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1039/C8GC02574F
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
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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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040
Artigo de periodico
Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones (2017)
Talero, Alexánder G.; Burtoloso, Antonio Carlos Bender
Source: Synlett. Unidade: IQSC
Assunto: FOTOQUÍMICA ORGÂNICA
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ABNT
TALERO, Alexánder G. e BURTOLOSO, Antonio Carlos Bender. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones. Synlett, v. 28, n. 14, p. 1748-1752, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1590977. Acesso em: 09 jun. 2024.
APA
Talero, A. G., & Burtoloso, A. C. B. (2017). Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones. Synlett, 28( 14), 1748-1752. doi:10.1055/s-0036-1590977
NLM
Talero AG, Burtoloso ACB. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones [Internet]. Synlett. 2017 ; 28( 14): 1748-1752.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1055/s-0036-1590977
Vancouver
Talero AG, Burtoloso ACB. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones [Internet]. Synlett. 2017 ; 28( 14): 1748-1752.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1055/s-0036-1590977
Artigo de periodico
Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides (2017)
Chiu, Megan; Metzker, Gustavo; Bernt, Christopher M; Tran, Anthony T.; Burtoloso, Antonio Carlos Bender ; Ford, Peter C
Source: ACS Sustainable Chemistry & Engineering. Unidade: IQSC
Assunto: CATÁLISE
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ABNT
CHIU, Megan et al. Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides. ACS Sustainable Chemistry & Engineering, v. 5, n. 4, p. 3158–3169, 2017Tradução . . Disponível em: https://doi.org/10.1021/acssuschemeng.6b02954. Acesso em: 09 jun. 2024.
APA
Chiu, M., Metzker, G., Bernt, C. M., Tran, A. T., Burtoloso, A. C. B., & Ford, P. C. (2017). Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides. ACS Sustainable Chemistry & Engineering, 5( 4), 3158–3169. doi:10.1021/acssuschemeng.6b02954
NLM
Chiu M, Metzker G, Bernt CM, Tran AT, Burtoloso ACB, Ford PC. Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides [Internet]. ACS Sustainable Chemistry & Engineering. 2017 ; 5( 4): 3158–3169.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1021/acssuschemeng.6b02954
Vancouver
Chiu M, Metzker G, Bernt CM, Tran AT, Burtoloso ACB, Ford PC. Probing the Lignin Disassembly Pathways with Modified Catalysts Based on Cu-Doped Porous Metal Oxides [Internet]. ACS Sustainable Chemistry & Engineering. 2017 ; 5( 4): 3158–3169.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1021/acssuschemeng.6b02954
Artigo de periodico
A comparative study of warheads for design of cysteine protease inhibitors (2017)
Silva, Daniel G da; Ribeiro, Jean Francisco Rosa; De Vita, Daniela; Cianni, Lorenzo; Franco, Caio Haddad; Freitas Junior, Lucio H; Moraes, Carolina Borsoi; Rocha, Josmar R; Burtoloso, Antonio Carlos Bender ; Kenny, Peter W; Leitão, Andrei ; Montanari, Carlos Alberto
Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC
Assunto: ALDEÍDOS
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ABNT
SILVA, Daniel G da et al. A comparative study of warheads for design of cysteine protease inhibitors. Bioorganic & Medicinal Chemistry Letters, v. 27, n. 22, p. 5031-5035, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2017.10.002. Acesso em: 09 jun. 2024.
APA
Silva, D. G. da, Ribeiro, J. F. R., De Vita, D., Cianni, L., Franco, C. H., Freitas Junior, L. H., et al. (2017). A comparative study of warheads for design of cysteine protease inhibitors. Bioorganic & Medicinal Chemistry Letters, 27( 22), 5031-5035. doi:10.1016/j.bmcl.2017.10.002
NLM
Silva DG da, Ribeiro JFR, De Vita D, Cianni L, Franco CH, Freitas Junior LH, Moraes CB, Rocha JR, Burtoloso ACB, Kenny PW, Leitão A, Montanari CA. A comparative study of warheads for design of cysteine protease inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27( 22): 5031-5035.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.bmcl.2017.10.002
Vancouver
Silva DG da, Ribeiro JFR, De Vita D, Cianni L, Franco CH, Freitas Junior LH, Moraes CB, Rocha JR, Burtoloso ACB, Kenny PW, Leitão A, Montanari CA. A comparative study of warheads for design of cysteine protease inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27( 22): 5031-5035.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.bmcl.2017.10.002
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1055/s-0035-1561061
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
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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: 09 jun. 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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1021/acs.orglett.6b01470
Artigo de periodico
Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents (2016)
Bernardim, Barbara; Cal, Pedro M. S. D.; Matos, Maria J.; Oliveira, Bruno L.; Martínez-Sáez, Nuria; Albuquerque, Inês S; Perkins, Elizabeth; Corzana, Francisco; Burtoloso, Antonio Carlos Bender ; Jiménez-Osés, Gonzalo; Bernardes, Gonçalo L. L.
Source: Nature Communications. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara et al. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents. Nature Communications, 2016Tradução . . Disponível em: https://doi.org/10.1038/ncomms13128. Acesso em: 09 jun. 2024.
APA
Bernardim, B., Cal, P. M. S. D., Matos, M. J., Oliveira, B. L., Martínez-Sáez, N., Albuquerque, I. S., et al. (2016). Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents. Nature Communications. doi:10.1038/ncomms13128
NLM
Bernardim B, Cal PMSD, Matos MJ, Oliveira BL, Martínez-Sáez N, Albuquerque IS, Perkins E, Corzana F, Burtoloso ACB, Jiménez-Osés G, Bernardes GLL. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents [Internet]. Nature Communications. 2016 ;[citado 2024 jun. 09 ] Available from: https://doi.org/10.1038/ncomms13128
Vancouver
Bernardim B, Cal PMSD, Matos MJ, Oliveira BL, Martínez-Sáez N, Albuquerque IS, Perkins E, Corzana F, Burtoloso ACB, Jiménez-Osés G, Bernardes GLL. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents [Internet]. Nature Communications. 2016 ;[citado 2024 jun. 09 ] Available from: https://doi.org/10.1038/ncomms13128
Artigo de periodico
Astaxanthin diferulate as a bifunctional antioxidant (2015)
Papa, Thiago Bueno Ruiz; Pinho, Vagner Dantas; Nascimento, Eduardo Sanches Pereira do; Santos, Willy Glen; Burtoloso, Antonio Carlos Bender ; Skibstede, Leif Horsfelt; Cardoso, Daniel Rodrigues
Source: Free Radical Research. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAPA, Thiago Bueno Ruiz et al. Astaxanthin diferulate as a bifunctional antioxidant. Free Radical Research, v. 49, n. 1, p. 102-111, 2015Tradução . . Disponível em: https://doi.org/10.3109/10715762.2014.982112. Acesso em: 09 jun. 2024.
APA
Papa, T. B. R., Pinho, V. D., Nascimento, E. S. P. do, Santos, W. G., Burtoloso, A. C. B., Skibstede, L. H., & Cardoso, D. R. (2015). Astaxanthin diferulate as a bifunctional antioxidant. Free Radical Research, 49( 1), 102-111. doi:10.3109/10715762.2014.982112
NLM
Papa TBR, Pinho VD, Nascimento ESP do, Santos WG, Burtoloso ACB, Skibstede LH, Cardoso DR. Astaxanthin diferulate as a bifunctional antioxidant [Internet]. Free Radical Research. 2015 ; 49( 1): 102-111.[citado 2024 jun. 09 ] Available from: https://doi.org/10.3109/10715762.2014.982112
Vancouver
Papa TBR, Pinho VD, Nascimento ESP do, Santos WG, Burtoloso ACB, Skibstede LH, Cardoso DR. Astaxanthin diferulate as a bifunctional antioxidant [Internet]. Free Radical Research. 2015 ; 49( 1): 102-111.[citado 2024 jun. 09 ] Available from: https://doi.org/10.3109/10715762.2014.982112
Artigo de periodico
LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements (2015)
Bernardim, Barbara; Hardman-Baldwin, Andrea M; Burtoloso, Antonio Carlos Bender
Source: RSC Advances. Unidade: IQSC
Assunto: QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e HARDMAN-BALDWIN, Andrea M e BURTOLOSO, Antonio Carlos Bender. LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements. RSC Advances, v. 5, n. 18, p. 13311-13314, 2015Tradução . . Disponível em: https://doi.org/10.1039/c4ra15670f. Acesso em: 09 jun. 2024.
APA
Bernardim, B., Hardman-Baldwin, A. M., & Burtoloso, A. C. B. (2015). LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements. RSC Advances, 5( 18), 13311-13314. doi:10.1039/c4ra15670f
NLM
Bernardim B, Hardman-Baldwin AM, Burtoloso ACB. LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements [Internet]. RSC Advances. 2015 ; 5( 18): 13311-13314.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1039/c4ra15670f
Vancouver
Bernardim B, Hardman-Baldwin AM, Burtoloso ACB. LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements [Internet]. RSC Advances. 2015 ; 5( 18): 13311-13314.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1039/c4ra15670f
Artigo de periodico
Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst (2015)
Metzker, Gustavo; Burtoloso, Antonio Carlos Bender
Source: Chemical Communications. Unidade: IQSC
Assunto: BIOMASSA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
METZKER, Gustavo e BURTOLOSO, Antonio Carlos Bender. Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst. Chemical Communications, v. 51, n. 75, p. 14199-14202, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5cc02993g. Acesso em: 09 jun. 2024.
APA
Metzker, G., & Burtoloso, A. C. B. (2015). Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst. Chemical Communications, 51( 75), 14199-14202. doi:10.1039/c5cc02993g
NLM
Metzker G, Burtoloso ACB. Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst [Internet]. Chemical Communications. 2015 ; 51( 75): 14199-14202.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1039/c5cc02993g
Vancouver
Metzker G, Burtoloso ACB. Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst [Internet]. Chemical Communications. 2015 ; 51( 75): 14199-14202.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1039/c5cc02993g
Artigo de periodico
Synthesis of alkaloids: Recent advances in the synthesis of phenanthroindolizidine alkaloids (2014)
Burtoloso, Antonio Carlos Bender ; Bertonha, Ariane Fernandes; Rosset, Isac George
Source: Current Topics in Medicinal Chemistry. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, ANTI-INFLAMATÓRIOS, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURTOLOSO, Antonio Carlos Bender e BERTONHA, Ariane Fernandes e ROSSET, Isac George. Synthesis of alkaloids: Recent advances in the synthesis of phenanthroindolizidine alkaloids. Current Topics in Medicinal Chemistry, v. 14, n. 2, p. 191-199, 2014Tradução . . Disponível em: https://doi.org/10.2174/1568026613666131213154633. Acesso em: 09 jun. 2024.
APA
Burtoloso, A. C. B., Bertonha, A. F., & Rosset, I. G. (2014). Synthesis of alkaloids: Recent advances in the synthesis of phenanthroindolizidine alkaloids. Current Topics in Medicinal Chemistry, 14( 2), 191-199. doi:10.2174/1568026613666131213154633
NLM
Burtoloso ACB, Bertonha AF, Rosset IG. Synthesis of alkaloids: Recent advances in the synthesis of phenanthroindolizidine alkaloids [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 2): 191-199.[citado 2024 jun. 09 ] Available from: https://doi.org/10.2174/1568026613666131213154633
Vancouver
Burtoloso ACB, Bertonha AF, Rosset IG. Synthesis of alkaloids: Recent advances in the synthesis of phenanthroindolizidine alkaloids [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 2): 191-199.[citado 2024 jun. 09 ] Available from: https://doi.org/10.2174/1568026613666131213154633
Artigo de periodico
A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal (2014)
Bernardim, Barbara; 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
BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, v. 70, p. 3291-3296, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.10.059. Acesso em: 09 jun. 2024.
APA
Bernardim, B., & Burtoloso, A. C. B. (2014). A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, 70, 3291-3296. doi:10.1016/j.tet.2013.10.059
NLM
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059
Vancouver
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059

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