The scope of the tungstic acid catalyzed hydroyen pe roxi de epoxidation of olefinic alcohols is exauined , at room temperature, i n buffered pr ot i c media. Epoxidation occurs with compl ete retention of configuration for bot h cis and tr ans al kenes . Chemoselectivity is dis cussed with respect
Stereoselective expoxidation of allylic and homoallylic alcohols with 30% hydrogen peroxide catalyzed by tungstic acid in buffered media
β Scribed by Denis Prat; Bernard Delpech; Robert Lett
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 222 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The aqueous tungstic acid-catalyzed hydrogen peroxide epoxidation of allyl i c al coho1s affo rds the same major di astereo i somer as the VO( acac) 2/tBu OOH system with quite connarab le stereoselectiviti es . In cont r ast , epoxidatIon of honeallylic al cohol s appears t o be much less stereos el ective.
π SIMILAR VOLUMES
## Abstract The highly chemoβ, regioβ, and diastereoselective and stereospecific epoxidation of various allylic alcohols with only one equivalent of hydrogen peroxide in water can be efficiently catalyzed by the dinuclear peroxotungstate, K~2~[{W(ο£ΎO)(O~2~)~2~(H~2~O)}~2~(ΞΌβO)]β 2βH~2~O (I). The cata