Issue 93, 2015

A rapid and selective synthesis of α,α-fluorohalo esters via fluorohalogenative or difluorinative hydration of ynol ethers

Abstract

A Selectfluor-mediated fluorohalogenative or difluorinative hydration of ynol ethers is described, giving various α,α-fluorohalo esters including α,α-bromofluoro, α,α-chlorofluoro, α,α-fluoroiodo, and α,α-difluoro derivatives in a highly selective manner under very mild reaction conditions. The resultant products can be applied to the facile synthesis of α-monofluoro-α-amino acids. This reaction represents a new advance in the trifunctionalization of alkynes.

Graphical abstract: A rapid and selective synthesis of α,α-fluorohalo esters via fluorohalogenative or difluorinative hydration of ynol ethers

Supplementary files

Article information

Article type
Communication
Submitted
06 Sep 2015
Accepted
21 Sep 2015
First published
22 Sep 2015

Chem. Commun., 2015,51, 16641-16644

Author version available

A rapid and selective synthesis of α,α-fluorohalo esters via fluorohalogenative or difluorinative hydration of ynol ethers

L. Hu, C. Che, Z. Tan and G. Zhu, Chem. Commun., 2015, 51, 16641 DOI: 10.1039/C5CC07471A

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