Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/18169
Title: Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine
Authors: Aksenov, D. A.
Аксенов, Д. А.
Arutiunov, N. A.
Арутюнов, Н. А.
Gasanova, A. Z.
Гасанова, А. З.
Aksenov, N. A.
Аксенов, Н. А.
Aksenov, A. V.
Аксенов, А. В.
Rubin, M. A.
Рубин, М. А.
Keywords: Alkaloids;Rearrangement;Cascade reactions;Nitroalkanes;Total synthesis
Issue Date: 2021
Publisher: Elsevier Ltd
Citation: Aksenov, D. A.; Arutiunov, N. A.; Gasanova, A. Z.; Aksenov, N. A.; Aksenov, A. V.; Lower, C.; Rubin, M. A. Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine // Tetrahedron Letters. - 2021. - Номер статьи 153395. - DOI 10.1016/j.tetlet.2021.153395
Series/Report no.: Tetrahedron Letters
Abstract: An innovative acid-assisted cascade transformation of indoles with 2-nitrostyrenes was developed, allowing for the one-pot assembly of heterocyclic scaffolds with four fused rings. This strategy was subsequently employed for the concise total synthesis of two natural products, the alkaloids norneocryptolepine and neocryptolepine
URI: http://hdl.handle.net/20.500.12258/18169
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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