Diastereoselective synthesis of dioxaadamantane skeletons from coumarin-fused bridged ketones via a triple Grignard addition and hydroalkoxylation sequence
Abstract
A sequential protocol involving triple allylic Grignard addition to coumarin-fused bridged ketones, followed by C–O bond-forming cyclization, is developed to access chromane-annulated dioxaadamantane skeletons with excellent diastereoselectivity.
Fields of Study & Subjects
Asymmetric Synthesis and Catalysis
Organic Chemistry Synthesis Methods
Advanced Synthetic Organic Chemistry
Publication details
- Journal / source
- Organic Chemistry Frontiers
- Volume
- 13
- Issue
- 8
- Pages
- 2360–2366
- Publication date
- 1 January 2026
- Language
- EN