Highly Enantioselective Direct Vinylogous Michael Addition of gamma-Butenolide to Enals
An unprecedented and simple direct vinylogous addition of deconjugated butenolide to enals has been developed in excellent stereoselectivities (>95% ee), with Aminal-PYrrolidine (APY) catalyst. This methodology allows for the efficient preparation of complex gamma-butenolide from readily available renewable resources. Furthermore, preliminary mechanistic investigations have allowed for the better understanding of the origin of both stereoselectivities and of the observed high reactivities.
Références
- Titre
- Highly Enantioselective Direct Vinylogous Michael Addition of gamma-Butenolide to Enals
- Type de publication
- Article de revue
- Année de publication
- 2011
- Auteurs
- Quintard, Adrien, Lefranc Alice, and Alexakis Alexandre
- Revue
- Organic Letters
- Volume
- 13
- Ticket
- 6
- Pagination
- 1540–1543
- ISSN
- 1523-7060
Soumis le 7 septembre 2022