Substituent effects on the photoisomerization of 5(E)-styryl-1,3-dimethyluracil
✍ Scribed by Sang Chul Shim; Cheon Seok Lee
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 918 KB
- Volume
- 50
- Category
- Article
- ISSN
- 1010-6030
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The reaction of dibenzylideneacetones or E,E-cinnamylidene-acetophenones and hydrazine hydrate provided 1-propionyl derivatives of 5-aryl-3-styryl-2-pyrazolines and 3-aryl-5-styryl-2-pyrazolines. These unsaturated ketones afforded 1-(2-carboxyphenyl) or 1-(4-carboxyphenyl) 5-aryl-3-styryl-2-pyrazoli
## Abstmct: The a@ sub&umts at positions 4 and 6 do not erert observable &unmic cffcts on the ting-chain tautomeric mtios of 2,4-or 2,6-aTaqbubstituted-tetmhydm-1,~~. On the other hand, the ekaivnic @ect of the Z-a~yl subs&em is mat&& in all eight seties s&die4 the equilibria CM be desctibed @ the