Two different rationalizations of magnetic non-equivalence of geminal methylene protons in ortho substituted N,N-diethylbenzamides and related compounds have been advanced. Bedford et ',';;T -\* and more recently Fulea and Krueger' advocate a "conformational effect", whereas Siddall and Garner3 and
On the origin of the magnetic non-equivalence of geminal NCH2 protons in thiobenzamides
β Scribed by Adrian O. Fulea; Peter J. Krueger
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 309 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The problem of the magnetic non-equivalence of geminal groups was dealt with extensively in the last decade.2a-g However, unambiguous information about the exact contribution of the con.
formatfonal and intrinsic asymmetry factors to ARAB is virtually non-existent.3
π SIMILAR VOLUMES
## Abstract Examples are given of the conformationally dependent influence of 3βsubstituents (methyl, __n__βpropyl, allyl, aryl, hydroxy and acyloxy) on the magnetic nonβequivalence of the benzylic methylene protons (N__CH__~2~Ph) of __N__βbenzylpiperidine as observable by ^1^H NMR. The results, to