| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 68508 | Journal of Molecular Catalysis A: Chemical | 2008 | 4 Pages |
Abstract
3,4-Epoxyalcohols undergo regioselective cyclization in the presence of CeCl3·7H2O in ref1uxing acetonitrile to afford tetrahydrofuran derivatives in good yields. On the other hand epoxyalcohols afforded 1-chloro-3-substituted-2-propanols under microwave irradiation using CeCl3·7H2O supported on SiO2 under solvent-free conditions.
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Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Gowravaram Sabitha, V. Rama Subba Rao, K. Sudhakar, M. Raj Kumar, E. Venkata Reddy, J.S. Yadav,