A Two-Step Synthesis of Unprotected 3-Aminoindoles via Post Functionalization with Nitrostyrene

A novel, low-cost method for the preparation of not easily accessible free 3-aminoindoles has been developed. This approach is based on a well-established reaction between indoles and nitrostyrene in the presence of phosphorous acid, which results in the formation of 4′-phenyl-4′H-spiro[indole-3,5′-...

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Autores principales:	Aksenov, N. A., Аксенов, Н. А., Arutiunov, N. A., Арутюнов, Н. А., Kurenkov, I. A., Куренков, И. А., Malyuga, V. V., Малюга, В. В., Aksenov, D. A., Аксенов, Д. А., Momotova, D. S., Момотова, Д. С., Zatsepilina, A. M., Зацепилина, А. М., Chukanova, E. A., Чуканова, Е. А., Leontiev, A. V., Леонтьев, А. В., Aksenov, A. V., Аксенов, А. В.
Formato:	Статья
Lenguaje:	English
Publicado:	2023
Materias:	Cascade transformations Phenylacetonitrile extrusion C3-amination of indoles
Acceso en línea:	https://dspace.ncfu.ru/handle/20.500.12258/24002
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https://dspace.ncfu.ru/handle/20.500.12258/24002

A Two-Step Synthesis of Unprotected 3-Aminoindoles via Post Functionalization with Nitrostyrene

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