Filtros : "Brocksom, Timothy J." Limpar

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  • Source: Journal of Flow Chemistry. Unidade: IFSC

    Subjects: SEDATIVOS, ANESTÉSICOS, COVID-19

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    • ABNT

      MARTINS , Guilherme M. et al. Scaled up and telescoped synthesis of propofol under continuous-flow conditions. Journal of Flow Chemistry, v. 12, n. 3, p. 371-379, 2022Tradução . . Disponível em: https://doi.org/10.1007/s41981-022-00234-0. Acesso em: 03 nov. 2024.
    • APA

      Martins , G. M., Magalhães, M. F. A., Brocksom, T. J., Bagnato, V. S., & Oliveira, K. T. de. (2022). Scaled up and telescoped synthesis of propofol under continuous-flow conditions. Journal of Flow Chemistry, 12( 3), 371-379. doi:10.1007/s41981-022-00234-0
    • NLM

      Martins GM, Magalhães MFA, Brocksom TJ, Bagnato VS, Oliveira KT de. Scaled up and telescoped synthesis of propofol under continuous-flow conditions [Internet]. Journal of Flow Chemistry. 2022 ; 12( 3): 371-379.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1007/s41981-022-00234-0
    • Vancouver

      Martins GM, Magalhães MFA, Brocksom TJ, Bagnato VS, Oliveira KT de. Scaled up and telescoped synthesis of propofol under continuous-flow conditions [Internet]. Journal of Flow Chemistry. 2022 ; 12( 3): 371-379.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1007/s41981-022-00234-0
  • Source: Global Journal of Science Frontier Research: B Chemistry. Unidade: IQSC

    Subjects: FUNGOS, BIOTRANSFORMAÇÃO

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      RIBEIRO, Sandra S et al. Analysis by GC-MS of an aza-michael eeaction catalyzed by CALB on an orbital shaker and under microwave irradiation. Global Journal of Science Frontier Research: B Chemistry, v. 14, n. 1, p. 7- 21, 2014Tradução . . Disponível em: https://globaljournals.org/GJSFR_Volume14/2-Analysis-by-GC-MS-of-an-Aza.pdf. Acesso em: 03 nov. 2024.
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      Ribeiro, S. S., Uliana, M. P., Brocksom, T. J., & Porto, A. L. M. (2014). Analysis by GC-MS of an aza-michael eeaction catalyzed by CALB on an orbital shaker and under microwave irradiation. Global Journal of Science Frontier Research: B Chemistry, 14( 1), 7- 21. Recuperado de https://globaljournals.org/GJSFR_Volume14/2-Analysis-by-GC-MS-of-an-Aza.pdf
    • NLM

      Ribeiro SS, Uliana MP, Brocksom TJ, Porto ALM. Analysis by GC-MS of an aza-michael eeaction catalyzed by CALB on an orbital shaker and under microwave irradiation [Internet]. Global Journal of Science Frontier Research: B Chemistry. 2014 ; 14( 1): 7- 21.[citado 2024 nov. 03 ] Available from: https://globaljournals.org/GJSFR_Volume14/2-Analysis-by-GC-MS-of-an-Aza.pdf
    • Vancouver

      Ribeiro SS, Uliana MP, Brocksom TJ, Porto ALM. Analysis by GC-MS of an aza-michael eeaction catalyzed by CALB on an orbital shaker and under microwave irradiation [Internet]. Global Journal of Science Frontier Research: B Chemistry. 2014 ; 14( 1): 7- 21.[citado 2024 nov. 03 ] Available from: https://globaljournals.org/GJSFR_Volume14/2-Analysis-by-GC-MS-of-an-Aza.pdf
  • Source: Photochemical and Photobiological Sciences. Unidade: IFSC

    Subjects: TERAPIA FOTODINÂMICA, BACTÉRIAS, FUNGOS

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      ULIANA, Marciana P. et al. Photobiological characteristics of chlorophyll a derivatives as microbial PDT agents. Photochemical and Photobiological Sciences, v. 13, n. 8, p. 1137-1145, 2014Tradução . . Disponível em: https://doi.org/10.1039/c3pp50376c. Acesso em: 03 nov. 2024.
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      Uliana, M. P., Pires, L., Pratavieira, S., Brocksom, T. J., Oliveira, K. T., Bagnato, V. S., & Kurachi, C. (2014). Photobiological characteristics of chlorophyll a derivatives as microbial PDT agents. Photochemical and Photobiological Sciences, 13( 8), 1137-1145. doi:10.1039/c3pp50376c
    • NLM

      Uliana MP, Pires L, Pratavieira S, Brocksom TJ, Oliveira KT, Bagnato VS, Kurachi C. Photobiological characteristics of chlorophyll a derivatives as microbial PDT agents [Internet]. Photochemical and Photobiological Sciences. 2014 ;13( 8): 1137-1145.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1039/c3pp50376c
    • Vancouver

      Uliana MP, Pires L, Pratavieira S, Brocksom TJ, Oliveira KT, Bagnato VS, Kurachi C. Photobiological characteristics of chlorophyll a derivatives as microbial PDT agents [Internet]. Photochemical and Photobiological Sciences. 2014 ;13( 8): 1137-1145.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1039/c3pp50376c
  • Source: Dyes and Pigments. Unidades: IQ, FFCLRP

    Subjects: QUÍMICA INORGÂNICA, SÍNTESE INORGÂNICA

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      SANTOS, Fabiane A. B. dos et al. Synthesis of functionalized chlorins sterically-prevented from self-aggregation. Dyes and Pigments, v. 99, n. 2, p. 402-411, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.05.024. Acesso em: 03 nov. 2024.
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      Santos, F. A. B. dos, Uchoa, A. F., Baptista, M. da S., Iamamoto, Y., Serra, O. A., Brocksom, T. J., & Oliveira, K. T. de. (2013). Synthesis of functionalized chlorins sterically-prevented from self-aggregation. Dyes and Pigments, 99( 2), 402-411. doi:10.1016/j.dyepig.2013.05.024
    • NLM

      Santos FAB dos, Uchoa AF, Baptista M da S, Iamamoto Y, Serra OA, Brocksom TJ, Oliveira KT de. Synthesis of functionalized chlorins sterically-prevented from self-aggregation [Internet]. Dyes and Pigments. 2013 ; 99( 2): 402-411.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
    • Vancouver

      Santos FAB dos, Uchoa AF, Baptista M da S, Iamamoto Y, Serra OA, Brocksom TJ, Oliveira KT de. Synthesis of functionalized chlorins sterically-prevented from self-aggregation [Internet]. Dyes and Pigments. 2013 ; 99( 2): 402-411.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
  • Source: Journal of Organic Chemistry. Unidade: FFCLRP

    Subjects: CATALASE, NIÓBIO

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      CONSTANTINO, Maurício Gomes et al. Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry, v. 71, p. 9880-9883, 2006Tradução . . Acesso em: 03 nov. 2024.
    • APA

      Constantino, M. G., Oliveira, K. T. de, Polo, E. C., Silva, G. V. J. da, & Brocksom, T. J. (2006). Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry, 71, 9880-9883.
    • NLM

      Constantino MG, Oliveira KT de, Polo EC, Silva GVJ da, Brocksom TJ. Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry. 2006 ; 71 9880-9883.[citado 2024 nov. 03 ]
    • Vancouver

      Constantino MG, Oliveira KT de, Polo EC, Silva GVJ da, Brocksom TJ. Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry. 2006 ; 71 9880-9883.[citado 2024 nov. 03 ]

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