| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5282532 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
The enolates formed from Lewis acid treatment of (2-trimethylsilylmethyl)cyclopropyl ketones react with in situ oxirane-derived aldehydes to generate aldol products that were easily transformed into 2-hydroxymethyl tetrahydrofurans under oxidation with m-chloroperoxybenzoic acid.
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Authors
Veejendra K. Yadav, Archana Gupta,