Cite
Molecular hybridization-guided 1,3-dipolar cycloaddition reaction enabled pyrimidine-fused spiropyrrolidine oxindoles synthesis as potential anticancer agents.
MLA
Liu, Xiong-Li, et al. “Molecular Hybridization-Guided 1,3-Dipolar Cycloaddition Reaction Enabled Pyrimidine-Fused Spiropyrrolidine Oxindoles Synthesis as Potential Anticancer Agents.” Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry, vol. 57, no. 39, Sept. 2016, pp. 4411–16. EBSCOhost, https://doi.org/10.1016/j.tetlet.2016.08.063.
APA
Liu, X.-L., Feng, T.-T., Jiang, W.-D., Yang, C., Tian, M.-Y., Jiang, Y., Lin, B., Zhao, Z., & Zhou, Y. (2016). Molecular hybridization-guided 1,3-dipolar cycloaddition reaction enabled pyrimidine-fused spiropyrrolidine oxindoles synthesis as potential anticancer agents. Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry, 57(39), 4411–4416. https://doi.org/10.1016/j.tetlet.2016.08.063
Chicago
Liu, Xiong-Li, Ting-Ting Feng, Wei-Dong Jiang, Chao Yang, Min-Yi Tian, Yan Jiang, Bing Lin, Zhi Zhao, and Ying Zhou. 2016. “Molecular Hybridization-Guided 1,3-Dipolar Cycloaddition Reaction Enabled Pyrimidine-Fused Spiropyrrolidine Oxindoles Synthesis as Potential Anticancer Agents.” Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry 57 (39): 4411–16. doi:10.1016/j.tetlet.2016.08.063.