Preparation and spectra of para-substituted 2,5-diphenyloxazoles
✍ Scribed by A.T. Balaban; L. Bîrlǎdeanu; I. Bally; P.T. Frangopol; M. Mocanu; Z. Simon
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 896 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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 spec
A series of 4-functionalised-2,5-diphenyloxazoles has been synthesised. Each member of the series has been assessed for the ability to scintillate in the presence of ionising radiation. The scintillation counting efficiency of each member of the series has been determined relative to 2,5diphenyloxaz