𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reactions of O-Benzoyl Oximes with Sodium Hydride. Substituted Isoxazoles and the Neber Rearrangement

✍ Scribed by Renfrow, W; White, J; Wolf, R; Bohl, W


Book ID
120300774
Publisher
American Chemical Society
Year
1968
Tongue
English
Weight
599 KB
Volume
33
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Studies on isoxazole and pyrazole format
✍ Lucjan Strekowski; Shou-Yuan Lin πŸ“‚ Article πŸ“… 1997 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 211 KB

## Abstract 5‐(2‐Aminophenyl)isoxazoles are obtained in good yields by the reaction of 2‐(trifluoromethyl)aniline with dilithio derivatives of oximes of acetone, 3‐pentanone, propiophenone, and cyclohexanone. An analogous synthesis of a substituted isoxazole from 4‐(trifluoromethyl)aniline and 3‐pe

Kinetics and mechanism of the reaction o
✍ Libor DuΕ‘ek; JaromΓ­r KavΓ‘lek; Vojeslav Ε tΔ›rba πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 107 KB πŸ‘ 2 views

The kinetics of reaction of substituted O-benzoylbenzamidoximes with sodium methoxide in methanol were studied at 25 Β°C. The only reaction products are substituted benzamidoximes and methyl benzoates. The slope of the dependence of rate constant on sodium methoxide concentration gradually increases,