对映选择合成
立体中心
化学
硒
路易斯酸
催化作用
硫化物
组合化学
有机化学
基础(拓扑)
立体化学
数学分析
数学
作者
Ren‐Fei Cao,Yu Lu,Yu-Xuan Huo,Yao Li,Xiao‐Song Xue,Zhi‐Min Chen
出处
期刊:Organic Letters
[American Chemical Society]
日期:2022-06-01
卷期号:24 (22): 4093-4098
被引量:20
标识
DOI:10.1021/acs.orglett.2c01731
摘要
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 4H-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.
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