Cobalt-Catalyzed Intramolecular [4 + 2] Cycloaddition of Cyclopropyl-Capped Dienes with Alkynes/Alkenes/Allene and Reaction Mechanism
A cobalt-catalyzed intramolecular [4 + 2] cycloaddition of cyclopropyl (CP)-capped dienes with ynes/enes/allene was reported, providing an efficient method toward a spiro[2.5]octene ring system found in natural products, such as illudin. The [4 + 2] cycloadducts can be converted into other compounds via CP chemistry. This reaction can also be catalyzed by Ni. A density functional theory study on the reaction mechanisms is also reported here.
Authors
- Liyan Kan (ORCID: https://orcid.org/0009-0009-3986-5910)
- Yi Zhou (ORCID: https://orcid.org/0000-0002-0273-007X)
- Lingquan Kong (ORCID: https://orcid.org/0000-0001-5705-9001)
- Zhi‐Xiang Yu (ORCID: https://orcid.org/0000-0003-0939-9727)
Institutions
- Peking University (CN)
- Beijing National Laboratory for Molecular Sciences (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2024-12-04
- DOI
- https://doi.org/10.1021/acs.orglett.4c03772
- Citations
- 3
- Primary Topic
- Catalytic Alkyne Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.75
Funders
- University of Cambridge
- National Natural Science Foundation of China