4,6-Diacetylresorcinol in Heterocyclic Synthesis, Part I: Synthesis and Biological Evaluation of Some New Linearly and Angularly Substituted Pyrano[3,2-g] Chromenes via Vilsmeier–Haack Formylation of 4,6-Diacetylresorcinol, Its Schiff Bases, and Hydrazones
Author:
Affiliation:
1. a Department of Chemistry , Faculty of Education, Ain Shams University , Roxy , Cairo , Egypt
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2013.783074
Reference33 articles.
1. Mild synthesis of N′-aryl-N,N-dimethylformamidinium chloride by Vilsmeier–Haack reagent
2. Selective synthesis of pyrazolo[3,4-d]pyrimidine, N-(1H-pyrazol-5-yl)formamide, or N-(1H-pyrazol-5-yl)formamidine derivatives from N-1-substituted-5-aminopyrazoles with new Vilsmeier-type reagents
3. Synthesis of new malonaldehyde derivatives using 2-heteroaryl-substituted trimethinium salts
4. Reactions of carbonyl compounds with (monohalo) methyleniminium salts (vilsmeier reagents)
5. The Synthesis of Pyridines, Quinolines and Other Related Systems by the Vilsmeier and the Reverse Vismeier Method
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