NMR spectroscopic structure elucidation of the products of the reaction of 3-(3-aryl-3-oxopropenyl)- chromen-4-ones with 1,2-phenylenediamine
✍ Scribed by Gábor Tóth; András Simon; Tímea Gondos; Albert Lévai; József Jekö; Ferenc Andrási
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 221 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1863
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The reaction of 3‐(3‐aryl‐3‐oxopropenyl)chromen‐4‐ones with 1,2‐phenylenediamine resulted in the unexpected formation of 10a‐aryl‐1,2,10,10a‐tetrahydrobenzo‐[4,5]‐imidazo[1,2‐a]pyridin‐3‐yl(2‐hydroxyphenyl)‐1‐methanones. Their structure elucidation and complete ^1^H and ^13^C assignments have been performed by a combination of various one‐ and two‐dimensional NMR experiments. Copyright © 2006 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract The synthesis of several 1‐acetyl‐3‐aryl‐5‐[3‐(2‐hydroxyphenyl)pyrazol‐4‐yl]‐2‐pyrazolines **3a**−**3h** has been accomplished by treatment of the 3‐(3‐aryl‐3‐oxopropenyl)chromen‐4‐ones **1a**−**h** with hydrazine hydrate in hot acetic acid. The 1‐acetyl‐3‐aryl‐5‐(3‐chromonyl)‐2‐pyrazol
## Abstract Nucleophilic addition of alkyl‐ and benzylthiols to benzoquinone diimine (**1**) gave the corresponding 3‐alkylthio‐ or 3‐benzylthio‐1,4‐phenylenediamines (**2**–**5**). However, addition of aryl‐ or heteroarylthiols to **1** formed 2‐arylthio‐ or 2‐heteroarylthio‐1,4‐phenylenediamines
## Dedicated to Professor Dr. Fritz Sauter on the occasion of his 75 th birthday 1-Acetyl-and 1-propionyl-2-pyrazolines 11-27 have been synthesized by the reaction of (3coumarinyl)chalcones 1-10 with hydrazine in hot acetic acid or propionic acid. While 5-aryl-3-(3coumarinyl)-1-phenyl-2-pyrazoline
## Abstract Propargylation of 3‐substituted‐1,2,4‐triazole‐5‐thiols, which predominantly exist as their thione tautomers, was carried out with the view to synthesize different heterocycles and study their biological activity. Three different products namely, a mono __S__‐propargyl and two __S__,__N