Filtros : "Advanced Synthesis and Catalysis" Limpar

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  • Source: Advanced Synthesis and Catalysis. Unidade: IQ

    Subjects: CANABINOIDES, FLAVONOIDES

    Acesso à fonteDOIHow to cite
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    • ABNT

      ALBALAT, Andreu Vidal e PAZ, Bruno Matos. Organocatalytic enantioselective syntheses of flavonoids and cannabinoids. Advanced Synthesis and Catalysis, 2023Tradução . . Disponível em: https://dx.doi.org/10.1002/adsc.202301168. Acesso em: 15 maio 2024.
    • APA

      Albalat, A. V., & Paz, B. M. (2023). Organocatalytic enantioselective syntheses of flavonoids and cannabinoids. Advanced Synthesis and Catalysis. doi:10.1002/adsc.202301168
    • NLM

      Albalat AV, Paz BM. Organocatalytic enantioselective syntheses of flavonoids and cannabinoids [Internet]. Advanced Synthesis and Catalysis. 2023 ;[citado 2024 maio 15 ] Available from: https://dx.doi.org/10.1002/adsc.202301168
    • Vancouver

      Albalat AV, Paz BM. Organocatalytic enantioselective syntheses of flavonoids and cannabinoids [Internet]. Advanced Synthesis and Catalysis. 2023 ;[citado 2024 maio 15 ] Available from: https://dx.doi.org/10.1002/adsc.202301168
  • Source: Advanced Synthesis and Catalysis. Unidade: IQ

    Subjects: CATÁLISE ASSIMÉTRICA, REAÇÕES QUÍMICAS, PALÁDIO

    Acesso à fonteDOIHow to cite
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    • ABNT

      POLO, Ellen Christine et al. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, v. 362, p. 884 – 892, 2020Tradução . . Disponível em: https://doi.org/10.1002/adsc.201901471. Acesso em: 15 maio 2024.
    • APA

      Polo, E. C., Wang, M. F., Angnes, R. A., Braga, A. A. C., & Correia, C. R. D. (2020). Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, 362, 884 – 892. doi:10.1002/adsc.201901471
    • NLM

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 maio 15 ] Available from: https://doi.org/10.1002/adsc.201901471
    • Vancouver

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 maio 15 ] Available from: https://doi.org/10.1002/adsc.201901471
  • Source: Advanced Synthesis and Catalysis. Unidade: FCF

    Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO

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    • ABNT

      OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 15 maio 2024.
    • APA

      Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142
    • NLM

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 maio 15 ] Available from: https://doi.org/10.1002/adsc.201900142
    • Vancouver

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 maio 15 ] Available from: https://doi.org/10.1002/adsc.201900142

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