𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A theoretical analysis of the conformations of monosubstituted napthalenes.

✍ Scribed by K. Sekigawa


Publisher
Elsevier Science
Year
1972
Tongue
French
Weight
27 KB
Volume
28
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A 1H NMR and theoretical investigation o
✍ Raymond J. Abraham; Paul Leonard; ClΓ‘udio F. Tormena πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 195 KB

## Abstract The complete analysis of the complex ^1^H NMR spectra of some monosubstituted cyclobutanes was achieved to give all the ^1^H chemical shifts and ^__n__^__J__~HH~ (__n__ = 2, 3 and 4) coupling constants in these molecules. The substituent chemical shifts of the substituents in the cyclob

A theoretical conformational analysis of
✍ Alberto L. Capparelli; Julio MaraΓ±on; Oscar M. Sorarrain; Roberto R. Filgueria πŸ“‚ Article πŸ“… 1974 πŸ› Elsevier Science 🌐 English βš– 333 KB
Theoretical analysis of fluoroglycine co
✍ Headley, Allan D.; Starnes, Stephen D. πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 185 KB πŸ‘ 2 views

Seven different optimized conformers of Ξ±-fluoroglycine (H 2 NCHFCOOH) were obtained from ab initio calculations. Some of these conformers are exceptionally stable compared to similar conformers of glycine. Conformers in which the lone pair of electrons on the nitrogen atom are antiperiplanar to the