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Title: | Two mutually complementary synthetic approaches towards 3‑substituted 3,4‑disubstituted and 1-(2‑pyridyl)-substituted isoquinolines |
Authors: | Nikonov, I. L. Kopchuk, D. S. Khasanov, A. F. Krinochkin, A. P. Starnovskaya, E. S. Shtaiz, Ya. K. Savchuk, M. I. Tanya, O. S. Zyryanov, G. V. Rusinov, V. L. Chupakhin, O. N. Зырянов, Г. В. |
Issue Date: | 2018 |
Publisher: | Уральский федеральный университет |
Citation: | Two mutually complementary synthetic approaches towards 3‑substituted 3,4‑disubstituted and 1-(2‑pyridyl)-substituted isoquinolines / I. L. Nikonov, D. S. Kopchuk, A. F. Khasanov, A. P. Krinochkin, E. S. Starnovskaya, Ya. K. Shtaiz, M. I Savchuk, O. S. Tanya, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin // Chimica Techno Acta. — 2018. — Vol. 5, No. 3. — P. 150-152. |
Abstract: | Two mutually complementary synthetic approaches towards 3- and 3,4‑disubstituted 1-(2‑pyridyl) isoquinolines were studied. The aryne-based method was successfully used for the obtaining of the corresponding the 3‑cyano-1-(2‑pyridyl) isoquinolines in one step / pot reaction, while it is unacceptable for the obtaining of other 1-(2‑pyridyl)isoquinolines. The enamine-based approach was successfully applied for the synthesis of other 1-(2‑pyridyl)isoquinolines, while it was unacceptable for the obtaining of 3‑cyano-1-(2‑pyridyl)isoquinolines. |
Keywords: | 1,2,4‑TRIAZINES ARYNES ENAMINES ISOQUNOLINES AZA-DIELS-ALDER REACTION DOMINOTRANSFRORMATION |
URI: | http://elar.urfu.ru/handle/10995/64661 |
RSCI ID: | https://elibrary.ru/item.asp?id=36379499 |
ISSN: | 2409-5613 (Print) 2411-1414 (Online) |
DOI: | 10.15826/chimtech.2018.5.3.04 |
Sponsorship: | This work was supported by the Russian Science Foundation (Reference № 18‑13‑00365). |
RSCF project card: | 18-13-00365 |
Origin: | Chimica Techno Acta. 2018. Vol. 5. № 3 |
Appears in Collections: | Chimica Techno Acta |
Files in This Item:
File | Description | Size | Format | |
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cta-2018-3-04.pdf | 605,17 kB | Adobe PDF | View/Open |
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