From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes

Abstract

Metal-catalyzed reductive coupling reactions between alkenes and alkynes are a long-standing tradition as a way to create complex unsaturated building blocks of value in organic synthesis ventures. Here, we review the general synthetic approaches realized under Co-catalysis utilizing chemical reductants, albeit with some limitations in scope and user-friendliness. A more recent advancement shows that these reductive ene–yne coupling reactions can also be accommodated by photoredox catalysis marking a stepping stone in the area, and creating new incentives for this kind of carbon–carbon bond formation and beyond.

Graphical abstract: From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Highlight
Submitted
15 nov 2024
Accepted
17 dec 2024
First published
19 dec 2024

Org. Chem. Front., 2025, Advance Article

From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes

B. L. Tóth, S. G. E. Amos and A. W. Kleij, Org. Chem. Front., 2025, Advance Article , DOI: 10.1039/D4QO02143F

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