Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/29804
Title: Convenient synthesis and antiproliferative activity of 2-(Indol-2-yl)-2-arylacetamides
Authors: Aksenov, D. A.
Аксенов, Д. А.
Kuzminov, I. K.
Кузьминов, И. К.
Arutiunov, N. A.
Арутюнов, Н. А.
Aleksandrova, E. V.
Александрова, Е. В.
Aksenov, A. V.
Аксенов, А. В.
Keywords: Acetamides;Neuroblastoma;Antiproliferative activity;Indole;Sodium borohydride
Issue Date: 2025
Publisher: Elsevier Ltd
Citation: Aksenov D.A., Fernandez G.E., Kuzminov I.K., Arutiunov N.A., Aleksandrova E.V., Aksenov A.V., Vernaza A., Ramirez J., Ross K., Smith J.L., Du L., Sathish P., Tantillo D.J., Kornienko A. Convenient synthesis and antiproliferative activity of 2-(Indol-2-yl)-2-arylacetamides // Tetrahedron. - 2025. - 175. - art. no. 134515. - DOI: 10.1016/j.tet.2025.134515
Series/Report no.: Tetrahedron
Abstract: There have been a limited number of reports describing the preparation of 2-(indol-2-yl)-2-arylacetamides and those syntheses that have been published suffer from significant drawbacks. In addition, this class of compounds has not been evaluated biologically despite the occurrence of 2-(indol-2-yl)-acetamides in natural products and medicinally important compounds. We developed a two-step synthesis of these compounds utilizing our previously developed preparation of 2-(3-oxoindolin-ylidene)-2-arylacetonitriles from o-nitroacetophenones and their transformation into the desired compounds utilizing a novel process involving treatment under mild conditions with NaBH4 in EtOH. The synthesized compounds were evaluated for antiproliferative effects against BE(2)-C neuroblastoma cells and two compounds were found to have micromolar IC50 values.
URI: https://dspace.ncfu.ru/handle/123456789/29804
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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