ChemInform Abstract: An Efficient and Stereoselective Conversion of Lactones to Substituted Cyclic Ethers.
β Scribed by H. YODA; M. MIZUTANI; K. TAKABE
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 38 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
An Efficient and Stereoselective Conversion of Lactones to Substituted Cyclic Ethers. -Cerium(III) chloride assisted addition of Grignard reagents to lactones and following BF 3 β’OEt 2 mediated deoxygenation of the resulting hemiketals [cf. (III)] with triethylsilane provides a general route to cyclic ethers. The process is also effective for the diastereoselective formation of cyclic ethers derived from monosubstituted tetrahydrofuranones. -(YODA,
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