Issue 16, 2022

Hypervalent iodine(iii)-mediated ring-expansive difluorination of alkynylcyclopropanes en route to the synthesis of difluorinated alkylidenecyclobutanes

Abstract

Described herein is a hypervalent iodine(III)-mediated ring-expansive difluorination of alkynylcyclopropanes using commercially available Olah's reagent (HF·Py) as the fluorine source. The approach allows the facile synthesis of difluorinated alkylidenecyclobutanes with mild reaction conditions and moderate to good yields. Mechanistic studies suggest that the reaction occurs via regioselective 1,2-fluoroiodination of a triple bond followed by a Wagner–Meerwein-type rearrangement.

Graphical abstract: Hypervalent iodine(iii)-mediated ring-expansive difluorination of alkynylcyclopropanes en route to the synthesis of difluorinated alkylidenecyclobutanes

Supplementary files

Article information

Article type
Research Article
Submitted
02 Jun 2022
Accepted
07 Jul 2022
First published
08 Jul 2022

Org. Chem. Front., 2022,9, 4447-4452

Hypervalent iodine(III)-mediated ring-expansive difluorination of alkynylcyclopropanes en route to the synthesis of difluorinated alkylidenecyclobutanes

S. Yang, X. Liu, S. Feng, Y. Li, F. Tu, B. Huang, L. Huang, Z. Huang, H. Wang and Q. Li, Org. Chem. Front., 2022, 9, 4447 DOI: 10.1039/D2QO00888B

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