Cite
Organocatalytic Enantioselective Michael Addition between 3‑(3-hydroxy‑1H‑pyrazol-1-yl)Oxindole and β-Nitrostyrene for the Preparation of Chiral Disubstituted Oxindoles.
MLA
Song, Xiang-Jia, et al. “Organocatalytic Enantioselective Michael Addition between 3‑(3-Hydroxy‑1H‑pyrazol-1-Yl)Oxindole and β-Nitrostyrene for the Preparation of Chiral Disubstituted Oxindoles.” Journal of Organic Chemistry, vol. 85, no. 14, July 2020, pp. 9290–300. EBSCOhost, https://doi.org/10.1021/acs.joc.9b03337.
APA
Song, X.-J., Ren, H.-X., Xiang, M., Li, C.-Y., Zou, Y., Li, X., Huang, Z.-C., Tian, F., & Wang, L.-X. (2020). Organocatalytic Enantioselective Michael Addition between 3‑(3-hydroxy‑1H‑pyrazol-1-yl)Oxindole and β-Nitrostyrene for the Preparation of Chiral Disubstituted Oxindoles. Journal of Organic Chemistry, 85(14), 9290–9300. https://doi.org/10.1021/acs.joc.9b03337
Chicago
Song, Xiang-Jia, Hong-Xia Ren, Min Xiang, Chen-Yi Li, Ying Zou, Xia Li, Zhi-Cheng Huang, Fang Tian, and Li-Xin Wang. 2020. “Organocatalytic Enantioselective Michael Addition between 3‑(3-Hydroxy‑1H‑pyrazol-1-Yl)Oxindole and β-Nitrostyrene for the Preparation of Chiral Disubstituted Oxindoles.” Journal of Organic Chemistry 85 (14): 9290–9300. doi:10.1021/acs.joc.9b03337.