𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Highly stereoselective reductions of α-alkoxy-β-keto esters. Aspects of the mechanism of sodium borohydride reduction of ketones in 2-propanol

✍ Scribed by Richard S. Glass; Donald R. Deardorff; Kevin Henegar


Publisher
Elsevier Science
Year
1980
Tongue
French
Weight
284 KB
Volume
21
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Highly stereoselective synthesis of eryt
✍ Tadashi Nakata; Tadasu Tanaka; Takeshi Oishi 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 253 KB

Erythro-a, B-epoxy alcohols were prepared in high stereoselectivity by zinc borohydride reduction of the corresponding a, B-epoxy ketones regardless of the substituents on the epoxide ring. Epoxidation of the ally1 alcohols (L) with tert-butyl hydroperoxide catalyzed by VO(acac)2 was reported to giv