Molecular Iodine–Catalyzed, Mild, Effective, Ecofriendly, Microwave-Assisted, One-Pot Synthesis of 5-Arylmethylidene-2-phenyloxazol-4-ones (Azalactones) Under Solvent-Free Conditions
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397910903162783
Reference5 articles.
1. Synthesis and immunomodulatory properties of selected oxazolone derivatives
2. A suitable synthesis of azlactones (4-benzylidene-2-phenyloxazolin-5-ones and 4-alkylidene-2-phenyloxazolin-5-ones) catalyzed by silica–alumina supported heteropolyacids
3. Molecular iodine catalyzed synthesis of aryl-14H-dibenzo[a, j]xanthenes under solvent-free condition
4. Zinc oxide (ZnO): An Efficient Catalyst for the Synthesis of 4-arylmethylidene-2-phenyl 5(4H)-oxazolones Having Antimicrobial Activity
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1. Rare demethylation of 4-benzylidene-2-phenyloxazolone;Synthetic Communications;2024-05-10
2. Synthesis of five-memberedO,N-heterocycles using metal and nonmetal;Synthetic Communications;2019-04-15
3. An ionic liquid gel: a heterogeneous catalyst for Erlenmeyer–Plochl and Henry reactions;New Journal of Chemistry;2018
4. A convenient synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones under solvent-assisted grinding;Tetrahedron Letters;2016-07
5. Triphenylphosphine (PPh3) Catalyzed Erlenmeyer Reaction for Azlactones under Solvent-free Conditions;Journal of Heterocyclic Chemistry;2016-03-15
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