Relay Catalysis-EnabledEnantioselective Annulationsof β,γ-Alkynyl-α-imino Esters with 1,3-Diones forthe Divergent Synthesis of Chiral Oxacycles
A novel protocol for the chemically divergent synthesis of chiral oxacycles has been developed using organo/metal relay catalysis. The methodology integrates a stereospecific Mannich reaction between β,γ-alkynyl-α-imino esters and 1,3-diones catalyzed by a chiral bifunctional squaramide, followed by Lewis acid-catalyzed regioselective annulation reactions. By switching the Lewis acid employed, we achieved a divergent pathway to construct structurally related pyran and furan derivatives from a common intermediate. The (3+3) and (3+2) annulation products were obtained in high yields and excellent stereoselectivities. Comprehensive mechanistic studies were conducted to establish the reaction mechanism.
Publication Details
- Journal
- Figshare
- Published
- 2025-02-19
- DOI
- https://doi.org/10.1021/acs.orglett.5c00233.s001
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00