Diastereoselective oxidative coupling of enolates of chiral carboxylic acid derivatives
✍ Scribed by Thomas Langer; Michael Illich; Günter Helmchen
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 224 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
## Abstract Dioxolanones **7** and **8a** and oxazolinones **9a** derived from pivalaldehyde and lactic acid, mandelic acid, and proline, respectively, furnish chiral enolates of type **3** by deprotonation with LDA. Reactions of these enolates with alkyl halides, aldehydes, and ketones **(→ 8b, 9b
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