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Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives

A number of 2,6-diazido-4-methylnicotinonitrile derivatives has been synthesized as prospective novel plant growth regulators. The 2-[(triphenylphosphoranylidene)amino]tetrazolo[1,5-a]pyridine derivative is selectively formed from 2,6-diazido-4-methylnicotinonitrile under the conditions of the Staud...

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Главные авторы: Aksenov, N. A., Аксенов, Н. А., Dotsenko, V. V., Доценко, В. В.
Формат: Статья
Язык:English
Опубликовано: Springer New York LLC 2018
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Online-ссылка:https://dspace.ncfu.ru/handle/20.500.12258/3537
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spelling ir-20.500.12258-35372025-02-12T13:04:57Z Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives Aksenov, N. A. Аксенов, Н. А. Dotsenko, V. V. Доценко, В. В. 1,2,3-triazoles Azidopyridines Dimroth reaction Growth regulating activity Iminophosphoranes Nicotinonitriles Staudinger reaction A number of 2,6-diazido-4-methylnicotinonitrile derivatives has been synthesized as prospective novel plant growth regulators. The 2-[(triphenylphosphoranylidene)amino]tetrazolo[1,5-a]pyridine derivative is selectively formed from 2,6-diazido-4-methylnicotinonitrile under the conditions of the Staudinger reaction, from which N-(6-azido-5-cyano-4-methylpyridin-2-yl)acylamides can be obtained by sequential reduction and acylation. The obtained azidopyridines are converted into the corresponding 1,2,3-triazoles when treated with 1,3-dicarbonyl compounds in the presence of Et3N. Field studies showed that some of the synthesized compounds were effective growth regulators of wheat 2018-12-03T14:10:01Z 2018-12-03T14:10:01Z 2018 Статья Dyadyuchenko, L.V., Dmitrieva, I.G., Aksenov, N.A., Dotsenko, V.V. Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives // Chemistry of Heterocyclic Compounds. - 2018. - Volume 54. - Issue 10. - Pages 964–970 http://hdl.handle.net/20.500.12258/3537 en Chemistry of Heterocyclic Compounds application/pdf application/pdf Springer New York LLC
institution СКФУ
collection Репозиторий
language English
topic 1,2,3-triazoles
Azidopyridines
Dimroth reaction
Growth regulating activity
Iminophosphoranes
Nicotinonitriles
Staudinger reaction
spellingShingle 1,2,3-triazoles
Azidopyridines
Dimroth reaction
Growth regulating activity
Iminophosphoranes
Nicotinonitriles
Staudinger reaction
Aksenov, N. A.
Аксенов, Н. А.
Dotsenko, V. V.
Доценко, В. В.
Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives
description A number of 2,6-diazido-4-methylnicotinonitrile derivatives has been synthesized as prospective novel plant growth regulators. The 2-[(triphenylphosphoranylidene)amino]tetrazolo[1,5-a]pyridine derivative is selectively formed from 2,6-diazido-4-methylnicotinonitrile under the conditions of the Staudinger reaction, from which N-(6-azido-5-cyano-4-methylpyridin-2-yl)acylamides can be obtained by sequential reduction and acylation. The obtained azidopyridines are converted into the corresponding 1,2,3-triazoles when treated with 1,3-dicarbonyl compounds in the presence of Et3N. Field studies showed that some of the synthesized compounds were effective growth regulators of wheat
format Статья
author Aksenov, N. A.
Аксенов, Н. А.
Dotsenko, V. V.
Доценко, В. В.
author_facet Aksenov, N. A.
Аксенов, Н. А.
Dotsenko, V. V.
Доценко, В. В.
author_sort Aksenov, N. A.
title Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives
title_short Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives
title_full Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives
title_fullStr Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives
title_full_unstemmed Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives
title_sort synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives
publisher Springer New York LLC
publishDate 2018
url https://dspace.ncfu.ru/handle/20.500.12258/3537
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