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Reductive Cleavage of 4′ H-Spiro[indole-3,5′-isoxazoles] en Route to 2-(1 H-Indol-3-yl)acetamides with Anticancer Activities

Reductive Cleavage of 4′ H-Spiro[indole-3,5′-isoxazoles] en Route to 2-(1 H-Indol-3-yl)acetamides with Anticancer Activities

Unusual cascade transformation involving ring opening and 1,2-alkyl shift was observed upon the reduction of 4′H-spiro[indole-3,5′-isoxazoles] or 2-(3-oxoindolin-2-yl)acetonitriles with sodium borohydride. This reaction allowed for expeditious and highly efficient preparation of 2-(1H-Indol-3-yl)ace...

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Главные авторы: Aksenov, A. V., Аксенов, А. В., Kirilov, N. K., Кирилов, Н. К., Arutiunov, N. A., Арутюнов, Н. А., Aksenov, D. A., Аксенов, Д. А., Kuzminov, I. K., Кузьминов, И. К., Aksenov, N. A., Аксенов, Н. А., Rubin, M. A., Рубин, М. А.
Format: Статья
Jezik:English
Izdano: American Chemical Society 2022
Teme:
Polycyclic aromatic hydrocarbons
Sodium Borohydride
Online dostop:https://dspace.ncfu.ru/handle/20.500.12258/21960
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https://dspace.ncfu.ru/handle/20.500.12258/21960

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