𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Preparation and NMR spectra of substituted 2-phenyl-5,5-dialkylimidazolinones

✍ Scribed by Miloš Sedlák; Aleš Halama; Petr Mitaš; Jaromír Kaválek; Vladimír Macháček


Publisher
Journal of Heterocyclic Chemistry
Year
1997
Tongue
English
Weight
334 KB
Volume
34
Category
Article
ISSN
0022-152X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Eighteen substituted 2‐phenyl‐5,5‐dialkylimidazolinones 2 have been prepared by cyclizations of substituted 2‐(N‐benzoylamino)alkanamides 1. The cyclization of methylamides 1 proceeds at room temperature whereas primary amides are cyclized on boiling. The ^1^H and ^13^C nmr spectra of the imidazolinones are presented and the changes in their spectra connected with their protonation in hexadeuteriodimethyl sulfoxide‐trifluoroacetic acid mixtures are discussed.


📜 SIMILAR VOLUMES


NMR-spectra of 1-[2,4,5-triphenylcyclope
✍ S. Wawzonek; W. E. Bennett 📂 Article 📅 1972 🏛 John Wiley and Sons 🌐 English ⚖ 136 KB

NMR-Spectra of 1-[2,4,5-triphenyl-2-cyclopentenyl]phenyl ketone and 1-[2,4,5-triphenyI-1 -cyclopentenyl]phenyl ketone indicate that the coupling constants of vicinal hydrogens in the cyclopentene ring vary with structure.

Preparation of 1-substituted-5-[(2-oxo-2
✍ Paula Aulaskari; Markku Ahlgrén; Pirjo Vainiotalo; Esko Pohjala 📂 Article 📅 2000 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 478 KB

## Abstract New high yield preparation methods were developed for the pharmaceutically interesting compounds, 1‐benzyl‐, 1‐methyl‐, and 1__H__‐5‐[(2‐oxo‐2‐phenyl)ethyl]imidazoles **1a‐c**, respectively. The title compounds were synthesized by four different methods using various starting materials.

Carbon-13 NMR spectra of some 4- and 5-s
✍ Gordon W. H. Cheeseman; Christopher J. Turner; Desmond J. Brown 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 299 KB

## Abstract Carbon‐13 NMR chemical shifts and carbon‐proton coupling constants for nine 4‐substituted and six 5‐substituted pyrimidines are reported. The carbon chemical shifts are correlated with π‐electron densities. Carbon‐proton coupling constants fail to correlate with substituent electronegat

1H and 13C NMR spectra of some 2-substit
✍ Miloslava Dandárová; Daniel Végh 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 202 KB

## Abstract ^1^H and ^13^C NMR spectra of 22 2‐substituted 4,5‐dimethylfurans are reported. The __J__(C, H) values were used for signal assignments and for the identification of geometrical isomers of some derivatives.