Subjects: HERBICIDAS, PRODUTOS NATURAIS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
ABNT
OOKA, Joey K et al. Synthesis and activity of 2-Acyl-cyclohexane-1,3-dione congeners derived from Peperomia natural products against the plant p-Hydroxyphenylpyruvate dioxygenase herbicidal molecular target site. Plants, v. 11, p. 1-18 art. 2269, 2022Tradução . . Disponível em: https://doi.org/10.3390/plants11172269. Acesso em: 12 out. 2024.APA
Ooka, J. K., Correia, M. V., Scotti, M. T., Fokoue, H. H., Yamaguchi, L. F., Kato, M. J., et al. (2022). Synthesis and activity of 2-Acyl-cyclohexane-1,3-dione congeners derived from Peperomia natural products against the plant p-Hydroxyphenylpyruvate dioxygenase herbicidal molecular target site. Plants, 11, 1-18 art. 2269. doi:10.3390/plants11172269NLM
Ooka JK, Correia MV, Scotti MT, Fokoue HH, Yamaguchi LF, Kato MJ, Dayan FE, Owens DK. Synthesis and activity of 2-Acyl-cyclohexane-1,3-dione congeners derived from Peperomia natural products against the plant p-Hydroxyphenylpyruvate dioxygenase herbicidal molecular target site [Internet]. Plants. 2022 ; 11 1-18 art. 2269.[citado 2024 out. 12 ] Available from: https://doi.org/10.3390/plants11172269Vancouver
Ooka JK, Correia MV, Scotti MT, Fokoue HH, Yamaguchi LF, Kato MJ, Dayan FE, Owens DK. Synthesis and activity of 2-Acyl-cyclohexane-1,3-dione congeners derived from Peperomia natural products against the plant p-Hydroxyphenylpyruvate dioxygenase herbicidal molecular target site [Internet]. Plants. 2022 ; 11 1-18 art. 2269.[citado 2024 out. 12 ] Available from: https://doi.org/10.3390/plants11172269