Cao Ren-Fei, Yu Lu, Huo Yu-Xuan, Li Yao, Xue Xiao-Song, Chen Zhi-Min
School of Chemistry and Chemical Engineering, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University, Shanghai 200240, P.R. China.
College of Chemistry, Nankai University, Tianjin 300071, P.R. China.
Org Lett. 2022 Jun 10;24(22):4093-4098. doi: 10.1021/acs.orglett.2c01731. Epub 2022 Jun 1.
An enantioselective selenocyclization of 1,1-disubstituted alkenes was achieved for the first time, which is enabled by a novel combination of a chiral BINAM-derived sulfide and an achiral Lewis acid. Various selenium-containing 4-3,1-benzoxazines, which are widely present in a range of medicinally relevant molecules, were readily obtained in moderate to good yields and good to excellent enantioselectivities. A series of tetrasubstituted carbon stereocenters were facilely constructed.