Organo-Manganese Reagents. Part 34. Enantioselective Synthesis of . delta.-Ketobutanolides from (L)-Glutamic Acid via Organo-Manganese Reagents. -It offers a new method to prepare δ-ketobutanolides which are interesting intermediates in the synthesis of biologically active natural products. -(CAH
Enantioselective synthesis of δ-ketobutanolides from (l)-glutamic acid via organomanganese reagents
✍ Scribed by Gérard Cahiez; Eric Métais
- Book ID
- 104361125
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 235 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0957-4166
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✦ Synopsis
Various optically active tS-ketobutanolides were easily prepared in good yields, with an excellent enantiomeric purity, by acylation of organomanganese reagents with the butyrolactone acid chloride 3 prepared from natural (L)-glutamic acid. The reaction takes place in THF under mild conditions (-10°C, 3h or 3% CuCI, -30°C, 20 min.
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