Issue 11, 2024

Modular synthesis of congested β2,2-amino acids via the merger of photocatalysis and oxidative functionalisations

Abstract

A two-step protocol for the modular synthesis of β2- and α-quaternary β2,2-amino acid derivatives is reported. The key steps are a photocatalytic hydroalkylation reaction, followed by an oxidative functionalisation to access N-protected β-amino acids, esters, and amides. This strategy can be effectively scaled up via continuous-flow technology.

Graphical abstract: Modular synthesis of congested β2,2-amino acids via the merger of photocatalysis and oxidative functionalisations

Supplementary files

Article information

Article type
Communication
Submitted
19 Dec 2023
Accepted
03 Jan 2024
First published
05 Jan 2024
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2024,60, 1456-1459

Modular synthesis of congested β2,2-amino acids via the merger of photocatalysis and oxidative functionalisations

K. Anwar, L. Capaldo, T. Wan, T. Noël and A. Gómez-Suárez, Chem. Commun., 2024, 60, 1456 DOI: 10.1039/D3CC06172H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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