Semisynthesis of prunetin, a bioactive O-methylated isoflavone from naringenin, by the sequential deacetylation of chalcone intermediates and oxidative rearrangement.

MLA

Sugai, Takeshi, et al. “Semisynthesis of Prunetin, a Bioactive O-Methylated Isoflavone from Naringenin, by the Sequential Deacetylation of Chalcone Intermediates and Oxidative Rearrangement.” Bioscience, Biotechnology, and Biochemistry, vol. 85, no. 1, Jan. 2021, pp. 143–47. EBSCOhost, https://doi.org/10.1093/bbb/zbaa021.

APA

Sugai, T., Hanaya, K., & Higashibayashi, S. (2021). Semisynthesis of prunetin, a bioactive O-methylated isoflavone from naringenin, by the sequential deacetylation of chalcone intermediates and oxidative rearrangement. Bioscience, Biotechnology, and Biochemistry, 85(1), 143–147. https://doi.org/10.1093/bbb/zbaa021

Chicago

Sugai, Takeshi, Kengo Hanaya, and Shuhei Higashibayashi. 2021. “Semisynthesis of Prunetin, a Bioactive O-Methylated Isoflavone from Naringenin, by the Sequential Deacetylation of Chalcone Intermediates and Oxidative Rearrangement.” Bioscience, Biotechnology, and Biochemistry 85 (1): 143–47. doi:10.1093/bbb/zbaa021.