Abstract
A palladium-catalyzed asymmetric intermolecular hydrocarboxylation of trisubstituted alkenes was reported, which afforded a series of succinic acid derivatives containing two chiral centers with moderate to excellent yields, enantioselectivity, and high diastereoselectivity. The resulting dimethyl succinates can be easily converted to optically active γ-butyrolactones, demonstrating the potential application of this method.
| Translated title of the contribution | Pd-Catalyzed Enantio- and Diastereo-selective Hydrocarboxylation of Trisubstituted Alkenes |
|---|---|
| Original language | Chinese (Traditional) |
| Pages (from-to) | 3249-3257 |
| Number of pages | 9 |
| Journal | Chinese Journal of Organic Chemistry |
| Volume | 44 |
| Issue number | 10 |
| DOIs | |
| State | Published - 25 Oct 2024 |