Multicomponent Synthesis of Pyrano[2,3- d ]pyrimidine Diones by the Reaction of Aldehydes with Malononitrile and Barbituric Acids Using a Carbocationic Catalytic System in Neutral Media
Author:
Affiliation:
1. Department of Chemical Engineering, Hamedan University of Technology, Hamedan, Iran
2. Chemistry Department, College of Sciences, Shiraz University, Shiraz, Iran
Publisher
Informa UK Limited
Link
https://www.tandfonline.com/doi/pdf/10.1080/00304948.2024.2368899
Reference41 articles.
1. l-Proline catalyzed multicomponent reaction of 3,4-dihydro-(2H)-pyran, urea/thiourea, and aldehydes: diastereoselective synthesis of hexahydropyrano pyrimidinones (thiones)
2. Proline–threonine dipeptide as an organocatalyst for the direct asymmetric aldol reaction
3. Trityl Chloride as a Novel and Efficient Organic Catalyst For Room Temperature Preparation of Bis(indolyl)methanes under Solvent-Free Conditions in Neutral Media
4. Triarylmethyl chlorides as novel, efficient, and mild organic catalysts for the synthesis of N-sulfonyl imines under neutral conditions
5. Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature
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