Enantiocontrol in Radical Coupling Reactions: A Catalytic [1,2]-Rearrangement of Allylic Ammonium Ylides
Abstract The [1,2]-rearrangement of ammonium ylides is a fascinating reaction that has captivated the mechanistically inclined for almost a century. Allylic migration of these ylides is dominated by a thermally allowed concerted [2,3]-rearrangement, with the [1,2]-process usually absent or a minor pathway. As such, development of a [1,2]-selective reaction within allylic systems is an uphill battle. Decades of mechanistic insights have not settled the debate on the true pathway for [1,2]-rearrangement, with a C–N homolysis step followed by a radical coupling within a solvent cage commonly accepted. Herein, we describe our journey through the development of such a process and opine on the broader context in which this chemistry may currently rest.
Authors
- Kevin Kasten (ORCID: https://orcid.org/0000-0003-1298-8784)
- Andrew D. Smith (ORCID: https://orcid.org/0000-0002-2104-7313)
- Will C. Hartley (ORCID: https://orcid.org/0000-0002-4789-7746)
Institutions
- University of St Andrews (GB)
- Universitat Rovira i Virgili (ES)
Publication Details
- Journal
- Synlett
- Published
- 2025-09-15
- DOI
- https://doi.org/10.1055/a-2702-3605
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University of Warwick
- Engineering and Physical Sciences Research Council