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Filtros : "Indexado no Chemical Abstracts" "SÍNTESE ORGÂNICA" Removidos: "ENZIMAS" "Budapest University of Technology and Economics, Hungary" "ICB-BMP" "ORNELLAS, FERNANDO REI" Limpar

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  • Artigo de periodico

    Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network (2021)

    Khalid, Muhammad ; Ali, Akbar ; Khan, Muhammad Usman ; Tahir, Muhammad Nawaz; Ahmad, Anees ; Ashfaq, Muhammad; Hussain, Riaz; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo

    Source: Journal of Molecular Structure. Unidades: IQ, IQSC

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      KHALID, Muhammad et al. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, v. 1230 p. 129827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129827. Acesso em: 15 out. 2024.

    • APA

      Khalid, M., Ali, A., Khan, M. U., Tahir, M. N., Ahmad, A., Ashfaq, M., et al. (2021). Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, 1230 p. 129827. doi:10.1016/j.molstruc.2020.129827

    • NLM

      Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 out. 15 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827

    • Vancouver

      Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 out. 15 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827

  • 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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      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: 15 out. 2024.

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      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 out. 15 ] 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 out. 15 ] 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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      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: 15 out. 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 out. 15 ] 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 out. 15 ] Available from: https://doi.org/10.1021/acs.joc.0c00833

  • Artigo de periodico

    Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii (2019)

    Matos, Iara Lisboa de ; Nitschke, Marcia ; Porto, Andre Luiz Meleiro

    Source: Marine Biotechnology. Unidade: IQSC

    Subjects: BIOTRANSFORMAÇÃO, SÍNTESE ORGÂNICA

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      MATOS, Iara Lisboa de e NITSCHKE, Marcia e PORTO, Andre Luiz Meleiro. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii. Marine Biotechnology, v. 21, p. 430-439 jun, 2019Tradução . . Disponível em: https://doi.org/10.1007/s10126-019-09893-y. Acesso em: 15 out. 2024.

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      Matos, I. L. de, Nitschke, M., & Porto, A. L. M. (2019). Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii. Marine Biotechnology, 21, 430-439 jun. doi:10.1007/s10126-019-09893-y

    • NLM

      Matos IL de, Nitschke M, Porto ALM. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii [Internet]. Marine Biotechnology. 2019 ; 21 430-439 jun.[citado 2024 out. 15 ] Available from: https://doi.org/10.1007/s10126-019-09893-y

    • Vancouver

      Matos IL de, Nitschke M, Porto ALM. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii [Internet]. Marine Biotechnology. 2019 ; 21 430-439 jun.[citado 2024 out. 15 ] Available from: https://doi.org/10.1007/s10126-019-09893-y

  • 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: 15 out. 2024.

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      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 out. 15 ] 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 out. 15 ] 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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      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: 15 out. 2024.

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      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 out. 15 ] 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 out. 15 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040

  • 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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      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: 15 out. 2024.

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      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 out. 15 ] 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 out. 15 ] Available from: https://doi.org/10.1055/s-0035-1561061

  • 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

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      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: 15 out. 2024.

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      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 out. 15 ] 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 out. 15 ] Available from: https://doi.org/10.3109/10715762.2014.982112

  • Artigo de periodico

    Zinc, lithium and magnesium carbenoids: chemical properties and relevant applications in organic synthesis (2015)

    Nishimura, Rodolfo H. V; Murie, Valter E; Soldi, Rafael A; Lopes, João Luís Callegari; Clososki, Giuliano Cesar

    Source: Journal of the Brazilian Chemical Society. Unidade: FCFRP

    Subjects: COMPOSTOS ORGANOMETÁLICOS, SÍNTESE ORGÂNICA, ZINCO, LÍTIO, MAGNÉSIO

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      NISHIMURA, Rodolfo H. V et al. Zinc, lithium and magnesium carbenoids: chemical properties and relevant applications in organic synthesis. Journal of the Brazilian Chemical Society, v. 26, n. 11, p. 2175-2188, 2015Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20150218. Acesso em: 15 out. 2024.

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      Nishimura, R. H. V., Murie, V. E., Soldi, R. A., Lopes, J. L. C., & Clososki, G. C. (2015). Zinc, lithium and magnesium carbenoids: chemical properties and relevant applications in organic synthesis. Journal of the Brazilian Chemical Society, 26( 11), 2175-2188. doi:10.5935/0103-5053.20150218

    • NLM

      Nishimura RHV, Murie VE, Soldi RA, Lopes JLC, Clososki GC. Zinc, lithium and magnesium carbenoids: chemical properties and relevant applications in organic synthesis [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 11): 2175-2188.[citado 2024 out. 15 ] Available from: https://doi.org/10.5935/0103-5053.20150218

    • Vancouver

      Nishimura RHV, Murie VE, Soldi RA, Lopes JLC, Clososki GC. Zinc, lithium and magnesium carbenoids: chemical properties and relevant applications in organic synthesis [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 11): 2175-2188.[citado 2024 out. 15 ] Available from: https://doi.org/10.5935/0103-5053.20150218

  • Artigo de periodico

    New approach to the synthesis of the natural product aripuanin (2015)

    Lazaro, Aline S; Ribeiro, Pedro H. Zana; Sairre, Mirela I; Donate, Paulo Marcos

    Source: Synthetic Communications. Unidade: FFCLRP

    Subjects: PRODUTOS NATURAIS (SÍNTESE QUÍMICA), SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      LAZARO, Aline S et al. New approach to the synthesis of the natural product aripuanin. Synthetic Communications, v. 45, n. 11, p. 1374-1378, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1021426. Acesso em: 15 out. 2024.

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      Lazaro, A. S., Ribeiro, P. H. Z., Sairre, M. I., & Donate, P. M. (2015). New approach to the synthesis of the natural product aripuanin. Synthetic Communications, 45( 11), 1374-1378. doi:10.1080/00397911.2015.1021426

    • NLM

      Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 out. 15 ] Available from: https://doi.org/10.1080/00397911.2015.1021426

    • Vancouver

      Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 out. 15 ] Available from: https://doi.org/10.1080/00397911.2015.1021426

  • Artigo de periodico

    Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil (2015)

    Andrade, Leandro Helgueira ; Sousa, Bruno A; Ferreira , Irlon Maciel; Porto, Andre Luiz Meleiro

    Source: Current Organic Synthesis. Unidades: IQ, IQSC

    Assunto: SÍNTESE ORGÂNICA

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      ANDRADE, Leandro Helgueira et al. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil. Current Organic Synthesis, v. 12, p. 696-713, 2015Tradução . . Disponível em: https://doi.org/10.2174/157017941206150828103404. Acesso em: 15 out. 2024.

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      Andrade, L. H., Sousa, B. A., Ferreira , I. M., & Porto, A. L. M. (2015). Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil. Current Organic Synthesis, 12, 696-713. doi:10.2174/157017941206150828103404

    • NLM

      Andrade LH, Sousa BA, Ferreira IM, Porto ALM. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil [Internet]. Current Organic Synthesis. 2015 ; 12 696-713.[citado 2024 out. 15 ] Available from: https://doi.org/10.2174/157017941206150828103404

    • Vancouver

      Andrade LH, Sousa BA, Ferreira IM, Porto ALM. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil [Internet]. Current Organic Synthesis. 2015 ; 12 696-713.[citado 2024 out. 15 ] Available from: https://doi.org/10.2174/157017941206150828103404

  • 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

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      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: 15 out. 2024.

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      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 out. 15 ] 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 out. 15 ] 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

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      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: 15 out. 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 out. 15 ] 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 out. 15 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059

  • Artigo de periodico

    Three-step synthesis of (+ )-preussin from decanal (2014)

    Rosset, Isac George; Dias, Rafael Mafra de Paula; Pinho, Vagner Dantas; Burtoloso, Antonio Carlos Bender

    Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      ROSSET, Isac George et al. Three-step synthesis of (+ )-preussin from decanal. Journal Organic Chemistry, v. 79, n. 14, p. 6748-6753, 2014Tradução . . Disponível em: https://doi.org/10.1021/jo5011558. Acesso em: 15 out. 2024.

    • APA

      Rosset, I. G., Dias, R. M. de P., Pinho, V. D., & Burtoloso, A. C. B. (2014). Three-step synthesis of (+ )-preussin from decanal. Journal Organic Chemistry, 79( 14), 6748-6753. doi:10.1021/jo5011558

    • NLM

      Rosset IG, Dias RM de P, Pinho VD, Burtoloso ACB. Three-step synthesis of (+ )-preussin from decanal [Internet]. Journal Organic Chemistry. 2014 ; 79( 14): 6748-6753.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo5011558

    • Vancouver

      Rosset IG, Dias RM de P, Pinho VD, Burtoloso ACB. Three-step synthesis of (+ )-preussin from decanal [Internet]. Journal Organic Chemistry. 2014 ; 79( 14): 6748-6753.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo5011558

  • Artigo de periodico

    Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones (2013)

    Rosset, Isac George; Burtoloso, Antonio Carlos Bender

    Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      ROSSET, Isac George e BURTOLOSO, Antonio Carlos Bender. Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones. Journal Organic Chemistry, v. 78, p. 9464-9470, 2013Tradução . . Disponível em: https://doi.org/10.1021/jo401191s. Acesso em: 15 out. 2024.

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      Rosset, I. G., & Burtoloso, A. C. B. (2013). Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones. Journal Organic Chemistry, 78, 9464-9470. doi:10.1021/jo401191s

    • NLM

      Rosset IG, Burtoloso ACB. Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones [Internet]. Journal Organic Chemistry. 2013 ; 78 9464-9470.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo401191s

    • Vancouver

      Rosset IG, Burtoloso ACB. Preparation of Z'alfa' e 'beta'-unsaturated diazoketones from Aldehydes: application in the Construction of Substituted Dihydropyridin-3-ones [Internet]. Journal Organic Chemistry. 2013 ; 78 9464-9470.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo401191s

  • Artigo de periodico

    Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines (2013)

    Bernardim, Barbara; Lordello, Leonardo D; Burtoloso, Antonio Carlos Bender

    Source: Current Topics in Medicinal Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      BERNARDIM, Barbara e LORDELLO, Leonardo D e BURTOLOSO, Antonio Carlos Bender. Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines. Current Topics in Medicinal Chemistry, v. 13, n. 17, p. 2099-2103, 2013Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf. Acesso em: 15 out. 2024.

    • APA

      Bernardim, B., Lordello, L. D., & Burtoloso, A. C. B. (2013). Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines. Current Topics in Medicinal Chemistry, 13( 17), 2099-2103. Recuperado de https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf

    • NLM

      Bernardim B, Lordello LD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines [Internet]. Current Topics in Medicinal Chemistry. 2013 ; 13( 17): 2099-2103.[citado 2024 out. 15 ] Available from: https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf

    • Vancouver

      Bernardim B, Lordello LD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines [Internet]. Current Topics in Medicinal Chemistry. 2013 ; 13( 17): 2099-2103.[citado 2024 out. 15 ] Available from: https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf

  • Artigo de periodico

    Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D (2012)

    Bernardim, Barbara; Pinho, Vagner D; Burtoloso, Antonio Carlos Bender

    Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      BERNARDIM, Barbara e PINHO, Vagner D e BURTOLOSO, Antonio Carlos Bender. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D. Journal Organic Chemistry, v. 77, n. 21, p. 9926-9931, 2012Tradução . . Disponível em: https://doi.org/10.1021/jo301967w. Acesso em: 15 out. 2024.

    • APA

      Bernardim, B., Pinho, V. D., & Burtoloso, A. C. B. (2012). Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D. Journal Organic Chemistry, 77( 21), 9926-9931. doi:10.1021/jo301967w

    • NLM

      Bernardim B, Pinho VD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D [Internet]. Journal Organic Chemistry. 2012 ; 77( 21): 9926-9931.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo301967w

    • Vancouver

      Bernardim B, Pinho VD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D [Internet]. Journal Organic Chemistry. 2012 ; 77( 21): 9926-9931.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo301967w

  • Artigo de periodico

    Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents (2011)

    Pinho, Vagner D; Burtoloso, Antonio Carlos Bender

    Source: Journal Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      PINHO, Vagner D e BURTOLOSO, Antonio Carlos Bender. Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents. Journal Organic Chemistry, v. 76, n. 5, p. 289-292, 2011Tradução . . Disponível em: https://doi.org/10.1021/jo1021844. Acesso em: 15 out. 2024.

    • APA

      Pinho, V. D., & Burtoloso, A. C. B. (2011). Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents. Journal Organic Chemistry, 76( 5), 289-292. doi:10.1021/jo1021844

    • NLM

      Pinho VD, Burtoloso ACB. Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents [Internet]. Journal Organic Chemistry. 2011 ; 76( 5): 289-292.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo1021844

    • Vancouver

      Pinho VD, Burtoloso ACB. Preparation of 'alfa' e 'beta'-unsaturated diazoketones employing a horner-wadsworth-emmons reagents [Internet]. Journal Organic Chemistry. 2011 ; 76( 5): 289-292.[citado 2024 out. 15 ] Available from: https://doi.org/10.1021/jo1021844

  • Artigo de periodico

    Dereplication of bromotyrosine-derived metabolites by LC-PDA-MS and analysis of the chemical profile of 14 aplysina sponge specimens from the brazilian coastline (2010)

    Silva, Michelli M; Bergamasco, Juliana; Lira, Simone Possedente de; Lopes, Norberto Peporine; Hadju, Eduardo; Peixinho, Solange; Berlinck, Roberto Gomes de Souza

    Source: Australian Journal of Chemistry. Unidades: FCFRP, IQSC, ESALQ

    Subjects: PRODUTOS NATURAIS, PORIFERA, METABÓLITOS SECUNDÁRIOS, SÍNTESE ORGÂNICA

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      SILVA, Michelli M et al. Dereplication of bromotyrosine-derived metabolites by LC-PDA-MS and analysis of the chemical profile of 14 aplysina sponge specimens from the brazilian coastline. Australian Journal of Chemistry, v. 63, n. 6, p. 886-894, 2010Tradução . . Disponível em: https://doi.org/10.1071/ch09616. Acesso em: 15 out. 2024.

    • APA

      Silva, M. M., Bergamasco, J., Lira, S. P. de, Lopes, N. P., Hadju, E., Peixinho, S., & Berlinck, R. G. de S. (2010). Dereplication of bromotyrosine-derived metabolites by LC-PDA-MS and analysis of the chemical profile of 14 aplysina sponge specimens from the brazilian coastline. Australian Journal of Chemistry, 63( 6), 886-894. doi:10.1071/ch09616

    • NLM

      Silva MM, Bergamasco J, Lira SP de, Lopes NP, Hadju E, Peixinho S, Berlinck RG de S. Dereplication of bromotyrosine-derived metabolites by LC-PDA-MS and analysis of the chemical profile of 14 aplysina sponge specimens from the brazilian coastline [Internet]. Australian Journal of Chemistry. 2010 ; 63( 6): 886-894.[citado 2024 out. 15 ] Available from: https://doi.org/10.1071/ch09616

    • Vancouver

      Silva MM, Bergamasco J, Lira SP de, Lopes NP, Hadju E, Peixinho S, Berlinck RG de S. Dereplication of bromotyrosine-derived metabolites by LC-PDA-MS and analysis of the chemical profile of 14 aplysina sponge specimens from the brazilian coastline [Internet]. Australian Journal of Chemistry. 2010 ; 63( 6): 886-894.[citado 2024 out. 15 ] Available from: https://doi.org/10.1071/ch09616

  • Artigo de periodico

    Synthesis and properties of new paramagnetic hybrid bayerite from Al(O)/napthalene dianhydride reaction (2010)

    Triboni, Eduardo Rezende; Silva, Mauro Francisco Pinheiro da; Finco, Alan Teruel; Rodrigues, Magali Aparecida; Demets, Grégoire Jean-François; Dyszy, Fabio Henrique; Isolani, Paulo Celso; Berci Filho, Pedro; Politi, Mário José

    Source: Materials Research. Unidades: FFCLRP, IQ, IQSC

    Subjects: FÍSICO-QUÍMICA ORGÂNICA, FOTOQUÍMICA, SÍNTESE ORGÂNICA

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      TRIBONI, Eduardo Rezende et al. Synthesis and properties of new paramagnetic hybrid bayerite from Al(O)/napthalene dianhydride reaction. Materials Research, v. 13, n. 4, p. 1-7, 2010Tradução . . Disponível em: https://doi.org/10.1590/S1516-14392010000400013. Acesso em: 15 out. 2024.

    • APA

      Triboni, E. R., Silva, M. F. P. da, Finco, A. T., Rodrigues, M. A., Demets, G. J. -F., Dyszy, F. H., et al. (2010). Synthesis and properties of new paramagnetic hybrid bayerite from Al(O)/napthalene dianhydride reaction. Materials Research, 13( 4), 1-7. doi:10.1590/S1516-14392010000400013

    • NLM

      Triboni ER, Silva MFP da, Finco AT, Rodrigues MA, Demets GJ-F, Dyszy FH, Isolani PC, Berci Filho P, Politi MJ. Synthesis and properties of new paramagnetic hybrid bayerite from Al(O)/napthalene dianhydride reaction [Internet]. Materials Research. 2010 ; 13( 4): 1-7.[citado 2024 out. 15 ] Available from: https://doi.org/10.1590/S1516-14392010000400013

    • Vancouver

      Triboni ER, Silva MFP da, Finco AT, Rodrigues MA, Demets GJ-F, Dyszy FH, Isolani PC, Berci Filho P, Politi MJ. Synthesis and properties of new paramagnetic hybrid bayerite from Al(O)/napthalene dianhydride reaction [Internet]. Materials Research. 2010 ; 13( 4): 1-7.[citado 2024 out. 15 ] Available from: https://doi.org/10.1590/S1516-14392010000400013

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