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
Revue
Organic Letters
Volume
13
Ticket
6
Pagination
1540–1543
ISSN
1523-7060
Soumis le 7 septembre 2022