Iodine Promoted Efficient Synthesis of 2-Arylimidazo[1,2-a]pyridines in Aqueous Media: A Comparative Study between Micellar Catalysis and an “On-Water” Platform
Author:
Affiliation:
1. Department of Chemistry, BITS Pilani-K. K. Birla Goa Campus, NH 17 B Bypass Road, Zuarinagar, Sancoale 403726, Goa, India
2. Parvatibai Chowgule College of Arts & Science (Autonomous), Margao 403602, Goa, India
Funder
Science and Engineering Research Board
Department of Science and Technology, Ministry of Science and Technology
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.0c01478
Reference88 articles.
1. aCouty, F.; Evano, G. In Comprehensive Heterocyclic Chemistry III; Katritzky, A. R., Ramsden, C. A., Scriven, E. F. V., Taylor, R. J. K., Eds. Elsevier: Oxford, 2008; Vol. 11, pp 409–499.
2. Recent Progress in the Pharmacology of Imidazo[1,2-a]pyridines
3. Imidazopyridines as a source of biological activity and their pharmacological potentials—Infrared and Raman spectroscopic evidence of their content in pharmaceuticals and plant materials
4. A novel imidazopyridine derivative, X22, prevents the retinal ischemia-reperfusion injury via inhibition of MAPKs
5. Inhibition of inflammation and oxidative stress by an imidazopyridine derivative X22 prevents heart injury from obesity
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