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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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 |
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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 |
| work_keys_str_mv |
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