Issue 19, 2024

Defluorinative functionalization of perfluoroalkyl alkenes with ureas: synthesis of C4-perfluoroalkenyl 2-imidazolones

Abstract

The C–F bond functionalization of polyfluoroalkyl substances has emerged as a significant research direction in the synthesis of organofluorides, owing to their unique chemical properties and potential synthetic applications. A defluorinative 1,2,3,4-tetrafunctionalization of perfluoroalkyl iodoalkenes with readily available ureas via multi-bond interconversion at four carbon sites has been developed. Taking advantage of the transformation of one C(sp2)–I, one C(sp2)–H, and two elusive C(sp3)–F bonds in a single reaction step, this transition-metal-free method provides facile access to a variety of perfluoroalkenyl 2-imidazolones. This protocol features a broad substrate scope, good functional group compatibility, moderate stereoselectivity, and mild reaction conditions.

Graphical abstract: Defluorinative functionalization of perfluoroalkyl alkenes with ureas: synthesis of C4-perfluoroalkenyl 2-imidazolones

Supplementary files

Article information

Article type
Research Article
Submitted
25 Jun 2024
Accepted
11 Aug 2024
First published
14 Aug 2024

Org. Chem. Front., 2024,11, 5538-5544

Defluorinative functionalization of perfluoroalkyl alkenes with ureas: synthesis of C4-perfluoroalkenyl 2-imidazolones

W. Han, M. Tang, Y. Chen, M. Ma, Z. Shen and X. Chu, Org. Chem. Front., 2024, 11, 5538 DOI: 10.1039/D4QO01173B

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