化学
环丙烷
组合化学
表面改性
有机化学
物理化学
戒指(化学)
作者
Renāte Melngaile,Arturs Sperga,Kim K. Baldridge,Janis Veliks
出处
期刊:Organic Letters
[American Chemical Society]
日期:2019-08-21
卷期号:21 (17): 7174-7178
被引量:28
标识
DOI:10.1021/acs.orglett.9b02867
摘要
Diarylfluoromethylsulfonium salts, alternatives to freons or advanced fluorinated building blocks, are bench stable and easy-to-use sources of direct fluoromethylene (:CHF) transfer to alkenes. These salts enabled development of a trans -selective monofluorinated Johnson–Corey–Chaykovsky reaction with vinyl sulfones or vinyl sulfonamides to access synthetically challenging monofluorocyclopropane scaffolds. The described method offers rapid access to monofluorinated cyclopropane building blocks with further functionalization opportunities to deliver more complex synthetic targets diastereoselectively.
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