APA aipamena

Dalton, D. M., Oberg, K. M., Yu, R. T., Lee, E. E., Perreault, S., Oinen, M. E., . . . Rovis, T. (2009). Enantioselective Rhodium-Catalyzed [2+2+2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model that Rationalizes Product Selectivity.

Chicago Style aipamena

Dalton, Derek M., Kevin M. Oberg, Robert T. Yu, Ernest E. Lee, Stéphane Perreault, Mark Emil Oinen, Melissa L. Pease, Guillaume Malik, and Tomislav Rovis. Enantioselective Rhodium-Catalyzed [2+2+2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model That Rationalizes Product Selectivity. 2009.

MLA aipamena

Dalton, Derek M., et al. Enantioselective Rhodium-Catalyzed [2+2+2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model That Rationalizes Product Selectivity. 2009.