Issue 27, 2019

Palladium-catalyzed formal insertion of carbenoids into N,O-aminals: direct access to α-alkoxy-β-amino acid esters

Abstract

A new and efficient reaction has been developed to synthesize α-alkoxy-β-amino acid esters via palladium-catalyzed selective formal insertion of carbenoids into N,O-aminals under mild reaction conditions. A broad range of α-diazoesters with different substituents and various N,O-aminals were compatible with this protocol, affording the corresponding α-alkoxy-β-amino acid esters in good to excellent yields.

Graphical abstract: Palladium-catalyzed formal insertion of carbenoids into N,O-aminals: direct access to α-alkoxy-β-amino acid esters

Supplementary files

Article information

Article type
Communication
Submitted
17 Feb 2019
Accepted
08 Mar 2019
First published
08 Mar 2019

Chem. Commun., 2019,55, 3947-3950

Palladium-catalyzed formal insertion of carbenoids into N,O-aminals: direct access to α-alkoxy-β-amino acid esters

W. Wang and H. Huang, Chem. Commun., 2019, 55, 3947 DOI: 10.1039/C9CC01374A

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