Source: Chirality. Unidade: IQSC
Assunto: CATÁLISE
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JIMENEZ, David et al. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, v. 31, p. 534-542, 2019Tradução . . Disponível em: https://doi.org/10.1002/chir.23078. Acesso em: 19 out. 2024.APA
Jimenez, D., Barreiro, J. C., Santos Júnior, F. M. dos, Vasconcellos, S., Vasconcellos, S. P. de, Porto, A. L. M., & Batista Junior, F. M. (2019). Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, 31, 534-542. doi:10.1002/chir.23078NLM
Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 out. 19 ] Available from: https://doi.org/10.1002/chir.23078Vancouver
Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 out. 19 ] Available from: https://doi.org/10.1002/chir.23078