SnCl4-Promoted Rearrangement of 2,3-Epoxy Alcohol Derivatives: Stereochemical Control of the Reaction.
β Scribed by Yasuyuki Kita; Satoshi Matsuda; Ryoko Inoguchi; Jnaneshwara K. Ganesh; Hiromichi Fujioka
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 36 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
A number of 2,3-epoxy alcohol derivatives (1-16), obtained either as racemates or through the Sharpless asymmetric epoxidation reaction, were studied on a Chiralcel OD column. Nearly all compounds exhibit good enantioselective resolution on this chiral support. The order of elution of enantiomers is