Imidazopyridine

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Federal government websites often end in. The site is secure. Box , United Arab Emirates. Fused pyridines are reported to display various pharmacological activities, such as antipyretic, analgesic, antiprotozoal, antibacterial, antitumor, antifungal, anti-inflammatory, and antiapoptotic. They are widely used in the field of medicinal chemistry.

Imidazopyridine

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This moiety is also useful in material science because of its structural character. Synthesis of this moiety from the easily available chemicals is desirable due to its tremendous use in the various branches of chemistry. Here we report a review on the synthesis of this scaffold employing different strategies such as condensation, multicomponent reactions, oxidative coupling, tandem reactions, aminooxygenation, and hydroamination reactions. Bagdi, S. Santra, K. Monir and A. Hajra, Chem.

This moiety is also useful in material science because of its structural character. Synthesis of this moiety from the easily available chemicals is desirable due to its tremendous use in the various branches of chemistry. Here we report a review on the synthesis of this scaffold employing different strategies such as condensation, multicomponent reactions, oxidative coupling, tandem reactions, aminooxygenation, and hydroamination reactions. Bagdi, S. Santra, K. Monir and A. Hajra, Chem. To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

Imidazopyridine

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Shaik 5 St. Puccini, A. Manage Catalog Rules. Cell Proteomics 15 , — An efficient synthesis of 3-aminoarylimidazo [1, 2-a] pyridines. The compounds exhibited pronounced bactericidal activity, as evidenced by their MIC and time-kill kinetics. Some IZP-based conjugates have been extensively utilized for the treatment of bacterial infections caused by wild or resistant bacteria. Figure Huang, Y. Delitto, D. Download PDF. Kamarul Monir. Contents move to sidebar hide.

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Xie et al. Prediction of cytotoxic activity of a series of 1H-pyrrolo [2, 3-b] pyridine derivatives as possible inhibitors of c-Met using molecular fingerprints. Accepted : 28 January A practical intramolecular C-H functionalization reaction of N -aryl enamines with molecular iodine as the sole oxidant in the presence of copper iodide CuI provides diverse imidazo[1,2- a ]pyridine and indole derivatives via I 2 -mediated oxidative C-N and C-C bond formation, respectively. Cited by. Figure 1. What type of issue did you experience with the content on the page? Main Menu. Cancer 17 , 1—14 Advanced search. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. Abignente E.