Issue 2, 2018

Radical-mediated synthesis of γ-lactones by copper-catalyzed intermolecular carboesterification of alkenes with α-carbonyl alkyl bromides and H2O

Abstract

A novel copper-catalyzed intermolecular carboesterification strategy of alkenes with α-carbonyl alkyl bromides is described. This reaction represents a facile and straightforward access to polysubstituted γ-lactone skeletons, including γ-lactones having ortho-substituted groups on the carbonyl group, in moderate to good yields via a radical strategy, which has good functional group tolerance.

Graphical abstract: Radical-mediated synthesis of γ-lactones by copper-catalyzed intermolecular carboesterification of alkenes with α-carbonyl alkyl bromides and H2O

Supplementary files

Article information

Article type
Research Article
Submitted
13 Jul 2017
Accepted
17 Sep 2017
First published
20 Sep 2017

Org. Chem. Front., 2018,5, 179-183

Radical-mediated synthesis of γ-lactones by copper-catalyzed intermolecular carboesterification of alkenes with α-carbonyl alkyl bromides and H2O

G. Pan, R. Song and J. Li, Org. Chem. Front., 2018, 5, 179 DOI: 10.1039/C7QO00579B

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