Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5220054 | Tetrahedron | 2012 | 10 Pages |
Abstract
The synthesis of six conjugates of l-proline and β-cyclodextrin and their evaluation as catalysts of aldol reaction in water are described. The results indicated that the nature of the linker between proline and β-cyclodextrin is important for catalytic activity; the one with the most flexible linker gave the best results. Inhibition experiments showed that the cavity of β-cyclodextrin plays a role in the catalysis. Permethylation of the cyclodextrin hydroxyl groups led to higher conversion rates.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Elisa G. Doyagüez, Alfonso Fernández-Mayoralas,