Cite
Conformational studies by dynamic NMR. stereomutation of the helical enantiomers of trigonal carbon diaryl-substituted compounds: dimesitylketone, dimesitylthioketone, and dimesitylethylene, 48
MLA
Grilli, Stefano, et al. “Conformational Studies by Dynamic NMR. Stereomutation of the Helical Enantiomers of Trigonal Carbon Diaryl-Substituted Compounds: Dimesitylketone, Dimesitylthioketone, and Dimesitylethylene, 48.” Journal of Organic Chemistry, vol. 66, no. 2, Jan. 2001, p. 488. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.82659790&authtype=sso&custid=ns315887.
APA
Grilli, S., Lunazzi, L., Mazzanti, A., Casarini, D., & Femoni, C. (2001). Conformational studies by dynamic NMR. stereomutation of the helical enantiomers of trigonal carbon diaryl-substituted compounds: dimesitylketone, dimesitylthioketone, and dimesitylethylene, 48. Journal of Organic Chemistry, 66(2), 488.
Chicago
Grilli, Stefano, Lodovico Lunazzi, Andrea Mazzanti, Daniele Casarini, and Cristina Femoni. 2001. “Conformational Studies by Dynamic NMR. Stereomutation of the Helical Enantiomers of Trigonal Carbon Diaryl-Substituted Compounds: Dimesitylketone, Dimesitylthioketone, and Dimesitylethylene, 48.” Journal of Organic Chemistry 66 (2): 488. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.82659790&authtype=sso&custid=ns315887.