Wu, Hsin-Yi Chang, Chih-Wei Chein, Rong-Jie Enantioselective Synthesis of (Thiolan-2-yl)diphenylmethanol and Its Application in Asymmetric, Catalytic Sulfur Ylide-Mediated Epoxidation This work describes an expeditious and efficient preparation of enantiopure (thiolan-2-yl)­diphenylmethanol (<b>2</b>) featuring a double nucleophilic substitution and Shi epoxidation as key steps. One of the applications of its benzyl ether derivative to asymmetric sulfur ylide-mediated epoxidation with up to 92% ee (14 examples) was also demonstrated herein. ee;Application;Sulfur;Catalytic;Asymmetric;application;Thiolan;sulfur;benzyl ether;Shi epoxidation;thiolan;nucleophilic substitution;preparation;enantiopure;EpoxidationThi;Enantioselective Synthesis 2013-06-07
    https://acs.figshare.com/articles/dataset/Enantioselective_Synthesis_of_Thiolan_2_yl_diphenylmethanol_and_Its_Application_in_Asymmetric_Catalytic_Sulfur_Ylide_Mediated_Epoxidation/2407843
10.1021/jo400648f.s002