Organocatalytic Addition on 1,2-Bis(sulfone)vinylenes Leading to an Unprecedented Rearrangement
An unprecedented rearrangement of 1,2-bis(sulfone)vinylenes used in aminocatalysis led to the formation of highly useful gem-disulfones. By using aminal–pyrrolidine organocatalysts, the 1,2-sulfone shift was generalised, leading to highly versatile adducts using both ketones and aldehydes. It represents a valuable alternative for the alpha-alkylation of carbonyl compounds.
Références
- Titre
- Organocatalytic Addition on 1,2-Bis(sulfone)vinylenes Leading to an Unprecedented Rearrangement
- Type de publication
- Article de revue
- Année de publication
- 2009
- Auteurs
- Quintard, Adrien, and Alexakis Alexandre
- Revue
- Chemistry – A European Journal
- Volume
- 15
- Pagination
- 11109–11113
Soumis le 7 septembre 2022