A general, highly enantioselective Michael addition of nitroalkanes to α,β-unsaturated enones catalyzed by 9-amino(9-deoxy)-epi-quinine: a remarkable additive effect.

MLA

Liu, Siyang, et al. “A General, Highly Enantioselective Michael Addition of Nitroalkanes to α,β-Unsaturated Enones Catalyzed by 9-Amino(9-Deoxy)-Epi-Quinine: A Remarkable Additive Effect.” Tetrahedron, vol. 72, no. 33, Aug. 2016, pp. 5115–20. EBSCOhost, https://doi.org/10.1016/j.tet.2016.07.008.

APA

Liu, S., Wang, Q., Ye, L., Shi, Z., Zhao, Z., Yang, X., Ding, K., & Li, X. (2016). A general, highly enantioselective Michael addition of nitroalkanes to α,β-unsaturated enones catalyzed by 9-amino(9-deoxy)-epi-quinine: a remarkable additive effect. Tetrahedron, 72(33), 5115–5120. https://doi.org/10.1016/j.tet.2016.07.008

Chicago

Liu, Siyang, Qingqing Wang, Ling Ye, Zhichuan Shi, Zhigang Zhao, Xuejun Yang, Keyi Ding, and Xuefeng Li. 2016. “A General, Highly Enantioselective Michael Addition of Nitroalkanes to α,β-Unsaturated Enones Catalyzed by 9-Amino(9-Deoxy)-Epi-Quinine: A Remarkable Additive Effect.” Tetrahedron 72 (33): 5115–20. doi:10.1016/j.tet.2016.07.008.