Investigation of Solvent Effect and H-Bonding on Spectroscopic Properties of 1-(3-Amino-6-(2,5-dichlorothiophen-3-yl)-4-phenylfuro[2,3-b]Pyridin-2-yl) Ethenone: Experimental and Computational Study

Author:

Abuflaha Rasha K.,Yousef Fakhri O.,Ghanem Raed,Al-Sou’od Khaldoun,Shahdi Ihsan A.,Almashaqbeh Omar K.,Al-Refai Mahmoud

Publisher

Springer Science and Business Media LLC

Subject

Law,Clinical Biochemistry,Spectroscopy,Sociology and Political Science,Social Sciences (miscellaneous),Clinical Psychology,Biochemistry

Reference34 articles.

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2. -Němec V, Hylsová M, Maier L, Flegel J, Sievers S, Ziegler S, Schroeder M, Berger BT, Chaikuad A, Valčá¼°ková B, Uldrijan S, Drápela S, Souček K, Waldmann H, Knapp S, Paruch K (2019) Furo[3,2-b]pyridine: a Privileged Scaffold for highly selective kinase inhibitors and effective modulators of the hedgehog pathway. Angew Chem Int Ed 58(4):1062–1066. https://doi.org/10.1002/anie.201810312

3. -Kumar RN, Poornachandra Y, Nagender P, Mallareddy G, Kumar NR, Ranjithreddy P, Kumar CG, Narsaiah B (2016) Synthesis of novel trifluoromethyl substituted furo[2,3-b]pyridine and pyrido[3′,2′:4,5]furo[3,2-d]pyrimidine derivatives as potential anticancer agents. Eur J Med Chem 108:68–78. https://doi.org/10.1016/j.ejmech.2015.11.007

4. -Ibrahim MM, AlRefai M, Azmi MN, Osman H, Abu Bakar MH, Geyer A (2019) Synthesis, characterization and cytotoxicity of new nicotinonitriles and their furo[2,3-b]pyridine derivatives. J Iran CHEM SOC 16:715–722. https://doi.org/10.1007/s13738-018-1549-y

5. -Němec V, Maier L, Berger BT, Chaikuad A, Drápela S, Souček K, Knapp S, Paruch K (2021) Highly selective inhibitors of protein kinases CLK and HIPK with the furo[3,2-b]pyridine core. Eur J Med Chem 215:113299. https://doi.org/10.1016/j.ejmech.2021.113299

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