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Filtros : "Gallo, Rafael D. C" Limpar

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1 - 8 (8 records)

  • 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

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    • 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: 25 jul. 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 jul. 25 ] 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 jul. 25 ] 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

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    • 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: 25 jul. 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 jul. 25 ] 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 jul. 25 ] 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

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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: 25 jul. 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 jul. 25 ] 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 jul. 25 ] Available from: https://doi.org/10.1021/acs.orglett.0c00540

  • Artigo de periodico

    Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis (2019)

    Gallo, Rafael D. C; Campovilla Junior, Orlando Celio; Ahmad, Anees; Burtoloso, Antonio Carlos Bender

    Source: Frontiers in Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      GALLO, Rafael D. C et al. Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis. Frontiers in Chemistry, v. 7, p. 1-7, 2019Tradução . . Disponível em: https://doi.org/10.3389/fchem.2019.00062. Acesso em: 25 jul. 2024.

    • APA

      Gallo, R. D. C., Campovilla Junior, O. C., Ahmad, A., & Burtoloso, A. C. B. (2019). Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis. Frontiers in Chemistry, 7, 1-7. doi:10.3389/fchem.2019.00062

    • NLM

      Gallo RDC, Campovilla Junior OC, Ahmad A, Burtoloso ACB. Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis [Internet]. Frontiers in Chemistry. 2019 ; 7 1-7.[citado 2024 jul. 25 ] Available from: https://doi.org/10.3389/fchem.2019.00062

    • Vancouver

      Gallo RDC, Campovilla Junior OC, Ahmad A, Burtoloso ACB. Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO4 Catalysis [Internet]. Frontiers in Chemistry. 2019 ; 7 1-7.[citado 2024 jul. 25 ] Available from: https://doi.org/10.3389/fchem.2019.00062

  • Trabalho de evento-resumo

    Green synthesis of oxazinanones: intramolecular cyclization of amino acid-derived diazoketones using a silica-supported HClO4 catalyst (2019)

    Campovilla Junior, Orlando Celio; Gallo, Rafael D. C; Ahmad, Anees; Burtoloso, Antonio Carlos Bender

    Source: Livro de Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química - SBQ. Unidade: IQSC

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA FARMACÊUTICA

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    • ABNT

      CAMPOVILLA JUNIOR, Orlando Celio et al. Green synthesis of oxazinanones: intramolecular cyclization of amino acid-derived diazoketones using a silica-supported HClO4 catalyst. 2019, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2019. Disponível em: https://repositorio.usp.br/directbitstream/2f0651f7-92a3-433d-8925-dc3eaa557576/P18129.pdf. Acesso em: 25 jul. 2024.

    • APA

      Campovilla Junior, O. C., Gallo, R. D. C., Ahmad, A., & Burtoloso, A. C. B. (2019). Green synthesis of oxazinanones: intramolecular cyclization of amino acid-derived diazoketones using a silica-supported HClO4 catalyst. In Livro de Resumos. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/2f0651f7-92a3-433d-8925-dc3eaa557576/P18129.pdf

    • NLM

      Campovilla Junior OC, Gallo RDC, Ahmad A, Burtoloso ACB. Green synthesis of oxazinanones: intramolecular cyclization of amino acid-derived diazoketones using a silica-supported HClO4 catalyst [Internet]. Livro de Resumos. 2019 ;[citado 2024 jul. 25 ] Available from: https://repositorio.usp.br/directbitstream/2f0651f7-92a3-433d-8925-dc3eaa557576/P18129.pdf

    • Vancouver

      Campovilla Junior OC, Gallo RDC, Ahmad A, Burtoloso ACB. Green synthesis of oxazinanones: intramolecular cyclization of amino acid-derived diazoketones using a silica-supported HClO4 catalyst [Internet]. Livro de Resumos. 2019 ;[citado 2024 jul. 25 ] Available from: https://repositorio.usp.br/directbitstream/2f0651f7-92a3-433d-8925-dc3eaa557576/P18129.pdf

  • 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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      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: 25 jul. 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 jul. 25 ] 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 jul. 25 ] Available from: https://doi.org/10.1039/C8GC02574F

  • Artigo de periodico

    Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones (2017)

    Gallo, Rafael D. C; Ahmad, Anees; Metzker, Gustavo; Burtoloso, Antonio Carlos Bender

    Source: Chemistry - A European Journal. Unidade: IQSC

    Assunto: HALOGENAÇÃO

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    • ABNT

      GALLO, Rafael D. C et al. Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones. Chemistry - A European Journal, v. 23, p. 16980-16984, 2017Tradução . . Disponível em: https://doi.org/10.1002/chem.201704609. Acesso em: 25 jul. 2024.

    • APA

      Gallo, R. D. C., Ahmad, A., Metzker, G., & Burtoloso, A. C. B. (2017). Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones. Chemistry - A European Journal, 23, 16980-16984. doi:10.1002/chem.201704609

    • NLM

      Gallo RDC, Ahmad A, Metzker G, Burtoloso ACB. Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones [Internet]. Chemistry - A European Journal. 2017 ; 23 16980-16984.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1002/chem.201704609

    • Vancouver

      Gallo RDC, Ahmad A, Metzker G, Burtoloso ACB. Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones [Internet]. Chemistry - A European Journal. 2017 ; 23 16980-16984.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1002/chem.201704609

  • Trabalho de evento-resumo

    OH insertion reactions catalised by bronsted acid (2017)

    Gallo, Rafael D. C; Burtoloso, Antonio Carlos Bender

    Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      GALLO, Rafael D. C e BURTOLOSO, Antonio Carlos Bender. OH insertion reactions catalised by bronsted acid. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf. Acesso em: 25 jul. 2024.

    • APA

      Gallo, R. D. C., & Burtoloso, A. C. B. (2017). OH insertion reactions catalised by bronsted acid. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf

    • NLM

      Gallo RDC, Burtoloso ACB. OH insertion reactions catalised by bronsted acid [Internet]. Proceedings. 2017 ;[citado 2024 jul. 25 ] Available from: https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf

    • Vancouver

      Gallo RDC, Burtoloso ACB. OH insertion reactions catalised by bronsted acid [Internet]. Proceedings. 2017 ;[citado 2024 jul. 25 ] Available from: https://repositorio.usp.br/directbitstream/705f23f3-95d2-4be6-884d-17bf41ed5052/P16981.pdf
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