Synthesis of 1-substituted 5-aryl-3-(3-coumarinyl)-2-pyrazolines by the reaction of 3-aryl-1-(3-coumarinyl)propen-1-ones with hydrazines
✍ Scribed by Albert Lévai; Jozsef Jekö; D. I. Brahmbhatt
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 89 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
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-pyrazolines 28-35 have been prepared by the reaction of (3-coumarinyl)chalcones 1,3,5-10 with phenylhydrazine in hot pyridine. Structures of all new compounds have been elucidated by microanalyses, 1 H and 13 C nmr spectroscopies.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract Regioselective epoxidation of 3‐aryl‐1‐(3‐coumarinyl)propen‐1‐ones **1–10** by isolated dimethyldioxirane afforded the appropriate epoxides **11–20** in high (76–87%) yields.
## Abstract magnified image 3‐(2‐Aryl‐2,3‐dihydro‐benzo[__b__][1,4]thiazepin‐4‐yl)chromen‐2‐ones (**2a, e, f**) and (__Z__)‐3‐(2,3‐dihydro‐2‐arylbenzo[__b__][1,4]thiazepin‐4(5__H__)‐ylidene)chroman‐2‐ones (**3a‐f**) have been synthesized by the reaction of 3‐aryl‐1‐(3‐coumarinyl)propen‐1‐ones (**1
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