𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Dynamic NMR study of cyclopropylcarbonyl fluoride. A comparison of the conjugating abilities of the cyclopropyl, vinyl, and phenyl groups

✍ Scribed by Noe, Eric A.; Young, Rose M.

Book ID
120342119
Publisher
American Chemical Society
Year
1982
Tongue
English
Weight
367 KB
Volume
104
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Dynamic NMR Study o
ChemInform Abstract: Dynamic NMR Study of Cyclopropanecarbaldehyde. Comparison of the Conjugating Abilities of the Cyclopropyl and Phenyl Groups.
✍ D. M. PAWAR; E. A. NOE πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 30 KB

Dynamic NMR Study of Cyclopropanecarbaldehyde. Comparison of the Conjugating Abilities of the Cyclopropyl and Phenyl Groups. -The NMR spectrum of cyclopropanecarbaldehyde shows two signals for the aldehyde proton at -162 β€’ C corresponding to a cis and a trans conformation with respect to the aldehy

Restricted rotation of the phenyl group
Restricted rotation of the phenyl group in Ξ²-hydroxyphosphonates: Dynamic NMR and semiempirical studies
✍ Nikolay G. Vassilev; Valentin S. Dimitrov πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 515 KB

## Abstract Free energies of activation, Ξ”__G__, for the rotation of the phenyl group in the range of 46.06–63.25 kJ mol^βˆ’1^ were observed in some model β‐hydroxyphosphonates. These barriers were found to depend on the type of substituents at the phosphorus atom and on the substituents at the β‐pos