Simple, Three-Component, Highly Efficient Green Synthesis of Thiazolo[3,2-a]pyridine Derivatives Under Neat Conditions
Author:
Affiliation:
1. a Chemistry Department, Faculty of Science, Minia University , El-Minia , Egypt
2. b Women Students–Medical Studies & Sciences Sections, Chemistry Department , College of Science, King Saud University , Riyadh , Saudi Arabia
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2010.505700
Reference19 articles.
1. Studies on Thiazolopyridines. Part 1: Antimicrobial Activity of Some Novel Fluorinated Thiazolo[3,2-a]Pyridines and Thiazolo[2′,3′:1,6]Pyrido[2,3-d]Pyrimidines
2. Discovery of novel α-glucosidase inhibitors based on the virtual screening with the homology-modeled protein structure
3. A Facile Synthesis of Some New Thiazolo[3, 2]pyridines Containing Pyrazolyl Moiety and Their Antimicrobial Activity
4. Dihydropyrimidine calcium channel blockers: 2-heterosubstituted 4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines
5. Virtual Screening Studies to Design Potent CDK2-Cyclin A Inhibitors
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