Issue 11, 2016

Non-stabilized enolates – versatile nucleophiles in transition metal-catalysed allylic alkylations

Abstract

While in the early days of palladium-catalyzed allylic alkylations mainly stabilized carbanions, such as malonates, have been used as standard nucleophiles, during the last 10–15 years also non stabilized enolates became more and more popular. Efficient protocols have been developed allowing their highly regio- as well as stereoselective allylations. In addition, catalysts based on other transition metals enlarge the synthetic potential of these valuable transformations, since each metal (complex) shows its own, typical reaction behaviour. This review will cover the new developments in this fast developing field.

Graphical abstract: Non-stabilized enolates – versatile nucleophiles in transition metal-catalysed allylic alkylations

Article information

Article type
Review Article
Submitted
09 May 2016
Accepted
16 Aug 2016
First published
23 Aug 2016

Org. Chem. Front., 2016,3, 1541-1560

Non-stabilized enolates – versatile nucleophiles in transition metal-catalysed allylic alkylations

U. Kazmaier, Org. Chem. Front., 2016, 3, 1541 DOI: 10.1039/C6QO00192K

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