A one-pot synthesis of 3-substituted-5-carbonylmethyl-1,2,4-oxadiazoles from β-keto esters and amidoximes under solvent-free conditions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. Discovery of Potent 3,5-Diphenyl-1,2,4-oxadiazole Sphingosine-1-phosphate-1 (S1P1) Receptor Agonists with Exceptional Selectivity against S1P2 and S1P3
2. Comparison of azabicyclic esters and oxadiazoles as ligands for the muscarinic receptor
3. Synthesis of (1-Azabicyclo(3.3.0)octanyl)methyl-Substituted Aromatic Heterocycles and Their Muscarinic Activity.
4. Novel 5-HT3 antagonists. Indole oxadiazoles
5. Selective Inhibitors of Monoamine Oxidase. 3. Structure−Activity Relationship of Tricyclics Bearing Imidazoline, Oxadiazole, or Tetrazole Groups
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1. Formation of 1,2,4-oxadiazole derivatives from Erlenmeyer azlactones and amidoximes;Monatshefte für Chemie - Chemical Monthly;2019-09-17
2. Hantzsch Reaction: A Greener and Sustainable Approach to 1,4-Dihydropyridines Using Non-commercial β-Ketoesters;Journal of Heterocyclic Chemistry;2018-09-11
3. General and Efficient Transesterification ofβ-Keto Esters with Various Alcohols Using Et3N as a Brønsted Base Additive;Synthetic Communications;2014-09-26
4. A novel one-pot synthesis of ferrocenyl-substituted 1,2,4-oxadiazoles;Journal of Organometallic Chemistry;2014-06
5. (3+2) Annulation of Amidinothioureas with Binucleophile: Synthesis and Antimicrobial Activity of 3-Phenylamino-5-aryl/alkyl-1,2,4-oxadiazole Derivatives;Journal of Heterocyclic Chemistry;2014-05-12
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