An easy synthesis of 5-functionally substituted ethyl 4-amino-1-aryl- pyrazolo-3-carboxylates: interesting precursors to sildenafil analogues
Author:
Publisher
Beilstein Institut
Subject
Organic Chemistry
Link
https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-3-15.pdf
Reference11 articles.
1. Comparison of different heterocyclic scaffolds as substrate analog PDE5 inhibitors
2. Synthesis and phosphodiesterase inhibitory activity of new sildenafil analogues containing a carboxylic acid group in the 5′-sulfonamide moiety of a phenyl ring
3. A convenient synthesis of pyrazolo[3,4-d]pyrimidine-4,6-dione and pyrazolo[4,3-d]pyrimidine-5,7-dione derivatives
4. Synthesis of some novel pyrazolo[3,4-d]pyrimidine derivatives as potential antimicrobial agents
5. Syntheses and Vasodilatory Activities of New Pyrazolo [4, 3-d] pyrimidin-7-ones1
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2. An efficient metal-free and catalyst-free C–S/C–O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amides;Beilstein Journal of Organic Chemistry;2023-03-02
3. Molecular Studies on Novel Antitumor Bis 1,4-Dihydropyridine Derivatives Against Lung Carcinoma and their Limited Side Effects on Normal Melanocytes;Anti-Cancer Agents in Medicinal Chemistry;2019-02-28
4. One-Pot and Efficient Synthesis of 5-Aminopyrazole-4-carbonitriles Catalyzed by Potassium Phthalimide;HETEROCYCLES;2017
5. A Facile, Improved Synthesis of Sildenafil and Its Analogues;Scientia Pharmaceutica;2015-10-18
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