Access to Fully Substituted Furans via Boryl Radical Catalyzed Cycloisomerization of Cyclopropenyl Ketones
Abstract We report the boryl radical catalyzed cycloisomerization of cyclopropenyl ketones to fully‐substituted furans, a type of highly important pharmacophore and synthetic intermediate. The reaction features neutral conditions, high yields, and toleration of variation at all possible positions of the substrate, making it an indispensable route for this type of important scaffold. Preliminary downstream transformation also revealed the synthetic potential of these furans in accessing other types of furans or more complex 3D scaffolds.
Authors
- Jiahang Li
- Xingran Yang
- Jinbo Zhao (ORCID: https://orcid.org/0000-0002-5261-7366)
Institutions
- Changchun University of Technology (CN)
Publication Details
- Journal
- Asian Journal of Organic Chemistry
- Published
- 2025-04-09
- DOI
- https://doi.org/10.1002/ajoc.202500126
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Natural Science Foundation of Jilin Province
- Changchun University of Technology
- National Natural Science Foundation of China
- People's Government of Jilin Province