Issue 38, 2018

Synthesis of α-amino ketones through aminations of umpoled enolates

Abstract

An efficient synthesis of α-amino ketones is developed using the umpolung strategy. Umpoled enolates such as N-alkenoxypyridinium salts react smoothly with diverse amines to give α-amino ketones via an SN2′ pathway. This umpolung strategy overcomes the drawbacks of traditional methods such as the need for prefunctionalized ketone derivatives. Our method also offers good chemical yields and high functional group tolerance.

Graphical abstract: Synthesis of α-amino ketones through aminations of umpoled enolates

Supplementary files

Article information

Article type
Paper
Submitted
16 Aug 2018
Accepted
07 Sep 2018
First published
07 Sep 2018

Org. Biomol. Chem., 2018,16, 6918-6922

Synthesis of α-amino ketones through aminations of umpoled enolates

X. Xia, B. Chen, X. Zeng and B. Xu, Org. Biomol. Chem., 2018, 16, 6918 DOI: 10.1039/C8OB02004C

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