硅烷
对映体药物
烯醇
催化作用
化学
对映选择合成
羟醛反应
烷基
硅烷
组合化学
有机化学
作者
Xiaowu Fang,Songwei Wen,Peishen Jin,Wenjing Bao,Shanshan Liu,Hengjiang Cong,Xiao Shen
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2022-01-27
卷期号:12 (4): 2150-2157
被引量:24
标识
DOI:10.1021/acscatal.2c00100
摘要
Fluorinated enol silanes are broadly useful in various synthetic transformations such as Mukaiyama aldol, Michael, and Mannich reactions. However, previous methods to these intermediates are limited to racemic synthesis. Therefore, the development of access to enantioenriched ones is of great value. We now describe an enantioselective reductive coupling reaction of fluoroalkylacylsilanes and 1,3-enynes. The coupling products were easily transformed to fluorinated enol silanes with the retention of enantiopurity though Brook rearrangement. The practicality of our methodology was demonstrated by the multisteps-one-isolation processes for the synthesis of alkynyl, alkenyl, and alkyl substituted enantioenriched β,β-difluoro enol silanes. The applications of the enantiopure β,β-difluoro enol silane in the synthesis of valuable chiral organofluorine compounds demonstrated the synthetic potential of our reaction.
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