𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The Stereochemistry of Ketonization. X. 1 Enols from α-Haloacids 2

✍ Scribed by Zimmerman, Howard E.; Cutshall, Theodore W.


Book ID
126111870
Publisher
American Chemical Society
Year
1959
Tongue
English
Weight
532 KB
Volume
81
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Influence of enolate geometry on the ste
✍ David A Oare; Clayton H Heathcock 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 207 KB

Preformed lithium enolates of ketones react with acyclic a,p-unsaturated ketones to give 1,5-diketones in good chemical yields. A strong correlation exists between enolate geometry and product stereochemistry; enolates having the z configuration provide anti addition products while E enolates usua

Influence of enolate geometry and struct
✍ Franklin A. Davis; Aurelia C. Sheppard; G.Sankar Lal 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 309 KB

The sfereoselectiviry for the asymmetric oxidation of enolafes to opfica//y active a-hydroxy ketones using (+)-( camphoryisulfonyi)oxaziridine is dependent on the enoiate substitution pattern, the solution structure of the enoiate and to a lesser extent the enoiate geometry Optically active a-hydrox