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Conversion of Some 2(3H)-Furanones into Pyrrolinotriazine and Oxazolopyrimidine Derivatives

✍ Scribed by Wael S. I. Abou-Elmagd; Ahmed I. Hashem


Book ID
115558844
Publisher
Journal of Heterocyclic Chemistry
Year
2012
Tongue
English
Weight
220 KB
Volume
49
Category
Article
ISSN
0022-152X

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Conversion of 2(3H)-furanones into 1,3,4
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## Abstract A series of 2‐phenyl‐5‐alkenyl‐1,3,4‐oxadiazoles were synthesized in high yields from the corresponding dicarbonylhydrazides through cyclodehydration. Β© 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:570–574, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DO

Conversion of 2(3H)-furanones bearing in
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## Abstract 2(3H)‐Furanones **__1a–d__** having exocyclic double bond and N‐acetylisatin nucleus were converted into the corresponding novel amides, pyrrolones, and imidazoles via nitrogen nucleophiles. All purposed structures were confirmed by NMR, mass spectra GC/MS, and chemical evidence. Β© 2003