APA (7th ed.) Citation

Yang, J., Cauble, D. F., Berro, A. J., Bauld, N. L., & Krische, M. J. (2004). Anion Radical [2 + 2] Cycloaddition as a Mechanistic Probe:   Stoichiometry- and Concentration-Dependent Partitioning of Electron-Transfer and Alkylation Pathways in the Reaction of the Gilman Reagent Me2CuLi·LiI with Bis(enones). Journal of organic chemistry, 69(23), 7979-7984. https://doi.org/10.1021/jo048499t

Chicago Style (17th ed.) Citation

Yang, Jingkui, David F. Cauble, Adam J. Berro, Nathan L. Bauld, and Michael J. Krische. "Anion Radical [2 + 2] Cycloaddition as a Mechanistic Probe:   Stoichiometry- and Concentration-Dependent Partitioning of Electron-Transfer and Alkylation Pathways in the Reaction of the Gilman Reagent Me2CuLi·LiI with Bis(enones)." Journal of Organic Chemistry 69, no. 23 (2004): 7979-7984. https://doi.org/10.1021/jo048499t.

MLA (9th ed.) Citation

Yang, Jingkui, et al. "Anion Radical [2 + 2] Cycloaddition as a Mechanistic Probe:   Stoichiometry- and Concentration-Dependent Partitioning of Electron-Transfer and Alkylation Pathways in the Reaction of the Gilman Reagent Me2CuLi·LiI with Bis(enones)." Journal of Organic Chemistry, vol. 69, no. 23, 2004, pp. 7979-7984, https://doi.org/10.1021/jo048499t.