Stereoselective syntheses of highly functionalized bicyclo[3.1.0]hexanes: a general methodology for the synthesis of potent and selective mGluR2/3 agonists.

MLA

Tan, Lushi, et al. “Stereoselective Syntheses of Highly Functionalized Bicyclo[3.1.0]Hexanes: A General Methodology for the Synthesis of Potent and Selective MGluR2/3 Agonists.” The Journal of Organic Chemistry, vol. 70, no. 20, Sept. 2005, pp. 8027–34. EBSCOhost, https://doi.org/10.1021/jo0511187.

APA

Tan, L., Yasuda, N., Yoshikawa, N., Hartner, F. W., Eng, K. K., Leonard, W. R., Tsay, F.-R., Volante, R. P., & Tillyer, R. D. (2005). Stereoselective syntheses of highly functionalized bicyclo[3.1.0]hexanes: a general methodology for the synthesis of potent and selective mGluR2/3 agonists. The Journal of Organic Chemistry, 70(20), 8027–8034. https://doi.org/10.1021/jo0511187

Chicago

Tan, Lushi, Nobuyoshi Yasuda, Naoki Yoshikawa, Frederick W Hartner, Kan Kaung Eng, William R Leonard, Fuh-Rong Tsay, Ralph P Volante, and Richard D Tillyer. 2005. “Stereoselective Syntheses of Highly Functionalized Bicyclo[3.1.0]Hexanes: A General Methodology for the Synthesis of Potent and Selective MGluR2/3 Agonists.” The Journal of Organic Chemistry 70 (20): 8027–34. doi:10.1021/jo0511187.