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
Revue
Chemistry – A European Journal
Volume
15
Pagination
11109–11113
Soumis le 7 septembre 2022