A carboxylic acid deoxygenation-based radical-polar crossover process for modular access to functionalized cyclopropanes
Abstract
Deoxygenation-initiated cyclopropanation: ketone-decorated cyclopropanes could be accessed via acylative coupling of (hetero)aryl carboxylic acids with 4-(pseudo)halo-1-alkenes.
Fields of Study & Subjects
Radical Photochemical Reactions
Cyclopropane Reaction Mechanisms
Catalytic C–H Functionalization Methods
Publication details
- Journal / source
- Organic & Biomolecular Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 24
- Issue
- 18
- Pages
- 3848–3852
- Publication date
- 1 January 2026
- Language
- EN