Highly Enantioselective Kinetic Resolution of Michael Adducts through N‐Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes.

MLA

Chen, Xiang‐Yu, et al. “Highly Enantioselective Kinetic Resolution of Michael Adducts through N‐Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes.” Chemistry - A European Journal, vol. 24, no. 39, July 2018, pp. 9735–38. EBSCOhost, https://doi.org/10.1002/chem.201802420.

APA

Chen, X., Li, S., Liu, Q., Kumar, M., Peuronen, A., Rissanen, K., & Enders, D. (2018). Highly Enantioselective Kinetic Resolution of Michael Adducts through N‐Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes. Chemistry - A European Journal, 24(39), 9735–9738. https://doi.org/10.1002/chem.201802420

Chicago

Chen, Xiang‐Yu, Sun Li, Qiang Liu, Mukesh Kumar, Anssi Peuronen, Kari Rissanen, and Dieter Enders. 2018. “Highly Enantioselective Kinetic Resolution of Michael Adducts through N‐Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes.” Chemistry - A European Journal 24 (39): 9735–38. doi:10.1002/chem.201802420.