𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cyclic imides IV. The reaction of some N-substituted nitrophthalimides with sodium methoxide

✍ Scribed by Lyman R. Caswell; Teresa Ling-Chun Kao


Book ID
112121475
Publisher
Journal of Heterocyclic Chemistry
Year
1966
Tongue
English
Weight
346 KB
Volume
3
Category
Article
ISSN
0022-152X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


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,

Heterogenous reactions. IV. The high tem
✍ Michael J. Tremelling; Steven P. Hopper; Jennifer Quirk πŸ“‚ Article πŸ“… 1977 πŸ› Elsevier Science 🌐 French βš– 110 KB

We have recently reported an efficient heterogeneous system which employs alkoxide bases as the solid phase substrate in reactions with vapor phase alkyl halides. ' In these previous systems the alkyl halides reacted almost exclusively with p-elimination, and the complication of solvolytic reactions