The Diastereoselective Epoxidation of Olefins in Supercritical Carbon Dioxide. -Under the optimized conditions shown, the title reactions can be carried out in a clean and selective manner. The use of non-toxic supercritical CO 2 in the presence of the new epoxidation vanadium catalyst leads to yie
โฆ LIBER โฆ
The diastereoselective epoxidation of olefins in supercritical carbon dioxide
โ Scribed by Geoffrey R Haas; Joseph W Kolis
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 207 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Allylic alcohols are epoxidized with tea-butyl hydroperoxide in the presence ofa vanadyl salen oxo-transfer catalyst in supercritical CO~ The metal catalyst was prepared in a simple two step, Schiffbase reaction to form the salen ligand, followed by complexation to the vanadyl group. The epoxidation reactions are clean and give both high yields and good diastereoselectivity.
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