Cite
Highly enantioselective hydroaminoalkylation of secondary amines catalyzed by group 5 metal amides with chiral biarylamidate ligandsElectronic supplementary information (ESI) available: Experimental procedures and crystallographic details. Molecular structure figures of 6–10. CCDC 775657–775663. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c0cc01265c
MLA
Zi, Guofu, et al. “Highly Enantioselective Hydroaminoalkylation of Secondary Amines Catalyzed by Group 5 Metal Amides with Chiral Biarylamidate LigandsElectronic Supplementary Information (ESI) Available: Experimental Procedures and Crystallographic Details. Molecular Structure Figures of 6–10. CCDC 775657–775663. For ESI and Crystallographic Data in CIF or Other Electronic Format See DOI: 10.1039/C0cc01265c.” Chemical Communications, vol. 46, no. 34, Sept. 2010, pp. 6296–98. EBSCOhost, https://doi.org/10.1039/c0cc01265c.
APA
Zi, G., Zhang, F., & Song, H. (2010). Highly enantioselective hydroaminoalkylation of secondary amines catalyzed by group 5 metal amides with chiral biarylamidate ligandsElectronic supplementary information (ESI) available: Experimental procedures and crystallographic details. Molecular structure figures of 6–10. CCDC 775657–775663. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c0cc01265c. Chemical Communications, 46(34), 6296–6298. https://doi.org/10.1039/c0cc01265c
Chicago
Zi, Guofu, Furen Zhang, and Haibin Song. 2010. “Highly Enantioselective Hydroaminoalkylation of Secondary Amines Catalyzed by Group 5 Metal Amides with Chiral Biarylamidate LigandsElectronic Supplementary Information (ESI) Available: Experimental Procedures and Crystallographic Details. Molecular Structure Figures of 6–10. CCDC 775657–775663. For ESI and Crystallographic Data in CIF or Other Electronic Format See DOI: 10.1039/C0cc01265c.” Chemical Communications 46 (34): 6296–98. doi:10.1039/c0cc01265c.