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Diastereoselective Monofluorocyclopropanation Using Fluoromethylsulfonium Salts

Authors :
Arturs Sperga
Renate Melngaile
Kim K. Baldridge
Janis Veliks
Source :
Organic Letters. 21:7174-7178
Publication Year :
2019
Publisher :
American Chemical Society (ACS), 2019.

Abstract

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.

Details

ISSN :
15237052 and 15237060
Volume :
21
Database :
OpenAIRE
Journal :
Organic Letters
Accession number :
edsair.doi.dedup.....555a33384bcae77f8ff6eaa8725e3df4