Issue 45, 2015

Brønsted acid-catalyzed 1,2-fluorine migration with fluoroepoxides

Abstract

A catalytic 1,2-fluorine migration reaction with simple fluoroepoxides at room temperature is reported. Under Brønsted acid catalysis, α-fluorinated ketones are efficiently constructed in the absence of an external fluorine source through a 1,2-fluorine migration reaction. The experimental results indicate that the present 1,2-fluorine migration reaction proceeds via a carbocation intermediate.

Graphical abstract: Brønsted acid-catalyzed 1,2-fluorine migration with fluoroepoxides

  • This article is part of the themed collection: Fluorine

Supplementary files

Article information

Article type
Paper
Submitted
03 Jun 2015
Accepted
21 Jul 2015
First published
22 Jul 2015

Dalton Trans., 2015,44, 19636-19641

Brønsted acid-catalyzed 1,2-fluorine migration with fluoroepoxides

T. Luo, R. Zhang, X. Shen, W. Zhang, C. Ni and J. Hu, Dalton Trans., 2015, 44, 19636 DOI: 10.1039/C5DT02088C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements