Diastereoselective Monofluorocyclopropanation Using Fluoromethylsulfonium Salts
Organic Letters 2019
Renāte Melngaile, A. Sperga, K.K. Baldridge, Jānis Veliks

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.


DOI
10.1021/acs.orglett.9b02867
Hyperlink
https://pubs.acs.org/doi/10.1021/acs.orglett.9b02867

Melngaile, R., Sperga, A., Baldridge, K., Veliks, J. Diastereoselective Monofluorocyclopropanation Using Fluoromethylsulfonium Salts. Organic Letters, 2019, Vol. 21, No. 17, pp.7174-7178. ISSN 1523-7060. Available from: doi:10.1021/acs.orglett.9b02867

Publication language
English (en)
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