Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine
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 norneocr...
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2021
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ir-20.500.12258-181692025-02-12T13:52:59Z Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine 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. Alkaloids Rearrangement Cascade reactions Nitroalkanes Total synthesis 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 2021-09-22T09:29:55Z 2021-09-22T09:29:55Z 2021 Статья 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 http://hdl.handle.net/20.500.12258/18169 en Tetrahedron Letters application/pdf application/pdf Elsevier Ltd |
| institution |
СКФУ |
| collection |
Репозиторий |
| language |
English |
| topic |
Alkaloids Rearrangement Cascade reactions Nitroalkanes Total synthesis |
| spellingShingle |
Alkaloids Rearrangement Cascade reactions Nitroalkanes Total synthesis 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. Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine |
| description |
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 |
| format |
Статья |
| author |
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. |
| author_facet |
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. |
| author_sort |
Aksenov, D. A. |
| title |
Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine |
| title_short |
Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine |
| title_full |
Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine |
| title_fullStr |
Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine |
| title_full_unstemmed |
Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine |
| title_sort |
synthetic studies towards benzofuro[2,3-b]quinoline and 6h-indolo[2,3-b]quinoline cores: total synthesis of norneocryptolepine and neocryptolepine |
| publisher |
Elsevier Ltd |
| publishDate |
2021 |
| url |
https://dspace.ncfu.ru/handle/20.500.12258/18169 |
| work_keys_str_mv |
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