‘Clip-Cycle’ approaches to functionalised pyrrolidines, pyrrolizidines and indolizidines

Abstract

The ‘Clip-Cycle’ approach is a versatile and modular synthetic method for the synthesis of aza-heterocycles via sequential cross metathesis and aza-Michael reactions. In this manuscript, a series of innovations to the ‘Clip-Cycle’ approach are reported. First, the asymmetric ‘Clip-Cycle’ syntheses of 2,5- and 3,5-pyrrolidines from chiral starting materials are reported for the first time, using a kinetic resolution method. A two-directional ‘Clip-Cycle’ approach for the synthesis of pyrrolizidines and indolizidines is then introduced.

Graphical abstract: ‘Clip-Cycle’ approaches to functionalised pyrrolidines, pyrrolizidines and indolizidines

Supplementary files

Article information

Article type
Paper
Submitted
06 Nov 2025
Accepted
12 Dec 2025
First published
15 Dec 2025
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2026, Advance Article

‘Clip-Cycle’ approaches to functionalised pyrrolidines, pyrrolizidines and indolizidines

L. C. Duff, S. Yilmaz, A. Agora, C. J. Maddocks, I. J. S. Fairlamb, W. P. Unsworth and P. A. Clarke, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D5OB01746G

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