Abstract
Pd-catalyzed asymmetric annulation via metal carbene is highly desired for efficient access to chiral cyclic compounds; however, such a strategy remains a considerable challenge. In this study, we report an unprecedented Pd-catalyzed asymmetric [4 + 1] annulation through a tandem carbene migratory insertion/Heck reaction, facilitated by an asymmetric ligand relay strategy. This approach provides an efficient protocol to access enantio-enriched α-alkylidene 3-substituted indanones. A wide range of substrates could be tolerated in the catalytic system, furnishing products with good to excellent enantioselectivity. A mechanistic study has also been conducted, which offers insights into the ligand relay catalytic system. Control experiments and DFT calculations elucidated a plausible novel E1cB mechanism for the elimination step of the Heck process, well explaining the generation of the olefin product of the Heck reaction bearing an unusual configuration. The enantio-determining step is revealed by DFT calculations to be a concerted process involving carbene formation and migratory insertion.
| Original language | English |
|---|---|
| Pages (from-to) | 4605-4614 |
| Number of pages | 10 |
| Journal | Journal of the American Chemical Society |
| Volume | 148 |
| Issue number | 4 |
| DOIs | |
| State | Published - 4 Feb 2026 |
Fingerprint
Dive into the research topics of 'Pd(II)-Catalyzed Asymmetric [4 + 1] Annulation via Ligand Relay-Enabled Carbenylative Insertion/E1cB-Type Heck Cascade'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver