Efficient synthesis of pyrano[2,3-b]pyridine derivatives using microwave or solar energy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Environmental Chemistry
Link
http://link.springer.com/article/10.1007/s10311-018-0744-5/fulltext.html
Reference19 articles.
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2. Azarifar D, Golbaghi M (2015) One pot synthesis of new series of pyranopyridine derivatives using 3-cyano-6-hydroxy-4-methylpyridin-2(1H)-one as a novel nucleophile. J Iran Chem Soc 12:1245–1251. https://doi.org/10.1007/s13738-015-0588-x
3. Azizi N, Dezfooli S (2016) Catalyst-free synthesis of imidazo[1,2-a]pyridines via Groebke multicomponent reaction. Environ Chem Lett 14:201–206. https://doi.org/10.1007/s10311-015-0541-3
4. Azuine MA, Tokuda H, Takayasu J, Enjyo F, Mukainaka T, Konoshima T, Nishino H, Kapadia G (2004) Cancer chemopreventive effect of phenothiazines and related tri-heterocyclic analogues in the 12-O-tetra-decanoylphorbol-13-acetate promoted Epstein-Barr virus early antigen activation and the mouse skin two-stage carcinogenesis models. Pharmacol Res 49:161–169. https://doi.org/10.1016/j.phrs.2003.07.014
5. Finlay HJ, Lloyd J, Nyman M, Conder ML, West T, Levesque P, Atwala K (2008) Pyrano- [2,3-b]pyridines as potassium channel antagonists. Bioorg Med Chem Lett 18:2714–2718. https://doi.org/10.1016/j.bmcl.2008.03.026
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