𝔖 Bobbio Scriptorium
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Regioselective synthesis of β-ketoesters from lithium enolates and methyl cyanoformate

✍ Scribed by Lewis N. Mander; S.Paul Sethi


Book ID
104221296
Publisher
Elsevier Science
Year
1983
Tongue
French
Weight
215 KB
Volume
24
Category
Article
ISSN
0040-4039

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✦ Synopsis


C-acyZation of lithium enolates by methyl cyanoformate provides high yieZds of B-keto esters under mild conditions and with ZOO% regioselectivity.


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✍ Michel Miesch; Gaëtan Mislin; Michel Franck-Neumann 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 228 KB

The enolates of cyclic ~-ketoesters react with electrophilic acetylenes to give the corresponding Michael adducts in good yields when the reaction is performed in acetone in the presence of catalytic amounts of K2CO 3. The Michael adducts resulting from ethynylmethylketone, when refluxed in toluene