| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5216965 | Tetrahedron | 2014 | 5 Pages |
Abstract
Supramolecular ionic organocatalysts and a metal-based catalyst were investigated in the ring-opening of epoxides by amines, without any artifice to enhance conversion (i.e., solvophobic effect, extended reaction time, heating, excess of amine, high catalyst loading). Different β-amino-alcohols were obtained in satisfying conversion (50-80%) in 24 h, under mild conditions.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Coralie Thomas, Sébastien Brut, Brigitte Bibal,