Diastereoselective Monofluorocyclopropanation Using Fluoromethylsulfonium Salts

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 wit...

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Veröffentlicht in:Organic letters 2019-09, Vol.21 (17), p.7174-7178
Hauptverfasser: Melngaile, Renate, Sperga, Arturs, Baldridge, Kim K, Veliks, Janis
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.9b02867