The enolate Claisen rearrangement of O-protected allylic glycolates yields functionalized acyclic systems with high syn and anti stereoselectivity. step in a short synthesis of threz-methylheptan-3-ol, This procedure is the key an aggregation pheromone of the European elm bark beetle.
โฆ LIBER โฆ
Ester-enolate Claisen rearrangement of lactic acid derivatives
โ Scribed by Bartlett, Paul A.; Tanzella, Donna J.; Barstow, James F.
- Book ID
- 118235259
- Publisher
- American Chemical Society
- Year
- 1982
- Tongue
- English
- Weight
- 706 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-3263
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