Issue 84, 2013

A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles

Abstract

The CF3SO3H-promoted ring opening of gem-difluorocyclopropyl ketones prefers to undergo proximal bond cleavage and the subsequent cyclization with nitriles occurred smoothly to give 2-fluoropyrroles.

Graphical abstract: A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2013
Accepted
28 Aug 2013
First published
29 Aug 2013

Chem. Commun., 2013,49, 9833-9835

A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles

T. Yang, J. Lin, Q. Chen and J. Xiao, Chem. Commun., 2013, 49, 9833 DOI: 10.1039/C3CC45456H

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