Novel synthetic approach to pyrrolo[1,2-b]cinnolines

Straightforward method for the synthesis of pyrrolo[1,2-b]cinnolines starting from 2-nitrobenzaldehydes and 2-methylfurans has been elaborated. The key steps of the process are oxidative furan ring opening with diazonium cation and intramolecular alkylation of azo group of the resulted cinnoline wit...

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Главные авторы:	Demidov, O. P., Демидов, О. П., Aksenov, N. A., Аксенов, Н. А.
Формат:	Статья
Язык:	English
Опубликовано:	Springer 2020
Темы:	Aza-heterocycles Cinnolines Furan ring opening Pyrrolo[1,2-b]cinnolines
Online-ссылка:	https://dspace.ncfu.ru/handle/20.500.12258/14300
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record_format	dspace
spelling	ir-20.500.12258-143002025-02-12T13:45:15Z Novel synthetic approach to pyrrolo[1,2-b]cinnolines Demidov, O. P. Демидов, О. П. Aksenov, N. A. Аксенов, Н. А. Aza-heterocycles Cinnolines Furan ring opening Pyrrolo[1,2-b]cinnolines Straightforward method for the synthesis of pyrrolo[1,2-b]cinnolines starting from 2-nitrobenzaldehydes and 2-methylfurans has been elaborated. The key steps of the process are oxidative furan ring opening with diazonium cation and intramolecular alkylation of azo group of the resulted cinnoline with secondary allyl alcohol 2020-10-07T13:39:53Z 2020-10-07T13:39:53Z 2020 Статья Plieva, A.T., Chalikidi, P.N., Gutnov, A.V., Turiev, A.M., Demidov, O.P., Aksenov, N.A., Magkoev, T.T., Abaev, V.T. Novel synthetic approach to pyrrolo[1,2-b]cinnolines // Chemistry of Heterocyclic Compounds. - 2020. - Volume 56. - Issue 8. - Pages 1030-1041 http://hdl.handle.net/20.500.12258/14300 en Chemistry of Heterocyclic Compounds application/pdf application/pdf Springer
institution	СКФУ
collection	Репозиторий
language	English
topic	Aza-heterocycles Cinnolines Furan ring opening Pyrrolo[1,2-b]cinnolines
spellingShingle	Aza-heterocycles Cinnolines Furan ring opening Pyrrolo[1,2-b]cinnolines Demidov, O. P. Демидов, О. П. Aksenov, N. A. Аксенов, Н. А. Novel synthetic approach to pyrrolo[1,2-b]cinnolines
description	Straightforward method for the synthesis of pyrrolo[1,2-b]cinnolines starting from 2-nitrobenzaldehydes and 2-methylfurans has been elaborated. The key steps of the process are oxidative furan ring opening with diazonium cation and intramolecular alkylation of azo group of the resulted cinnoline with secondary allyl alcohol
format	Статья
author	Demidov, O. P. Демидов, О. П. Aksenov, N. A. Аксенов, Н. А.
author_facet	Demidov, O. P. Демидов, О. П. Aksenov, N. A. Аксенов, Н. А.
author_sort	Demidov, O. P.
title	Novel synthetic approach to pyrrolo[1,2-b]cinnolines
title_short	Novel synthetic approach to pyrrolo[1,2-b]cinnolines
title_full	Novel synthetic approach to pyrrolo[1,2-b]cinnolines
title_fullStr	Novel synthetic approach to pyrrolo[1,2-b]cinnolines
title_full_unstemmed	Novel synthetic approach to pyrrolo[1,2-b]cinnolines
title_sort	novel synthetic approach to pyrrolo[1,2-b]cinnolines
publisher	Springer
publishDate	2020
url	https://dspace.ncfu.ru/handle/20.500.12258/14300
work_keys_str_mv	AT demidovop novelsyntheticapproachtopyrrolo12bcinnolines AT demidovop novelsyntheticapproachtopyrrolo12bcinnolines AT aksenovna novelsyntheticapproachtopyrrolo12bcinnolines AT aksenovna novelsyntheticapproachtopyrrolo12bcinnolines
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Novel synthetic approach to pyrrolo[1,2-b]cinnolines

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