Issue 6, 2017

A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid

Abstract

An effective palladium-catalyzed sequential carbonylation of olefins with formic acid is described. Ketones and the corresponding α,β-enones can be obtained with up to 90% yield. The reaction process is operationally simple and requires no toxic CO.

Graphical abstract: A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid

Supplementary files

Article information

Article type
Research Article
Submitted
09 ဖေ 2017
Accepted
22 ဖေ 2017
First published
22 ဖေ 2017

Org. Chem. Front., 2017,4, 1074-1078

A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid

W. Chang, J. Dai, J. Li, Y. Shi, W. Ren and Y. Shi, Org. Chem. Front., 2017, 4, 1074 DOI: 10.1039/C7QO00111H

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