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The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide

The action of 2,3-dimethylbenzothiazol-3-ium iodide on 1H-benzo[f]chromenes containing an acceptor substituent in the β-position to the oxygen atom in the presence of triethylamine results in the opening of the pyran ring and the formation of [(2E,4Z)-4-(3-methyl-benzothiazol-2(3H)-ylidene)but-2-en-...

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मुख्य लेखकों: Demidov, O. P., Демидов, О. П.
स्वरूप: Статья
भाषा:English
प्रकाशित: 2023
विषय:
ऑनलाइन पहुंच:https://dspace.ncfu.ru/handle/20.500.12258/22265
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spelling ir-20.500.12258-222652023-01-26T15:00:59Z The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide Demidov, O. P. Демидов, О. П. 2,3-dimethylbenzothiazol-3-ium iodide Electron-deficient 1H-benzo[f]chromenes Push-pull 1,3-dienes Michael reaction Thiacyanine dyes The action of 2,3-dimethylbenzothiazol-3-ium iodide on 1H-benzo[f]chromenes containing an acceptor substituent in the β-position to the oxygen atom in the presence of triethylamine results in the opening of the pyran ring and the formation of [(2E,4Z)-4-(3-methyl-benzothiazol-2(3H)-ylidene)but-2-en-1-yl]naphthalen-2-ols. In the case of 1-aryl-2-nitro-1H-benzo[f]chromenes, 3-methyl-2-[(1E,3Z)-3-(3-methylbenzothiazol-2(3H)-ylidene)prop-1-en-1-yl]benzothiazol-3-ium iodide was isolated. The resulting compounds containing the merocyanine chromophore are of interest as dyes and fluorescent labels. 2023-01-26T15:00:14Z 2023-01-26T15:00:14Z 2022 Статья Korzhenko, K.S., Osyanin, V.А., Osipov, D.V., Rashchepkina, D.А., Demidov, O.P., Klimochkin, Y.N. The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide // Chemistry of Heterocyclic Compounds. - 2022. - 58 (11), pp. 634-638. - DOI: 10.1007/s10593-022-03137-z http://hdl.handle.net/20.500.12258/22265 en Chemistry of Heterocyclic Compounds application/pdf application/pdf
institution СКФУ
collection Репозиторий
language English
topic 2,3-dimethylbenzothiazol-3-ium iodide
Electron-deficient 1H-benzo[f]chromenes
Push-pull 1,3-dienes
Michael reaction
Thiacyanine dyes
spellingShingle 2,3-dimethylbenzothiazol-3-ium iodide
Electron-deficient 1H-benzo[f]chromenes
Push-pull 1,3-dienes
Michael reaction
Thiacyanine dyes
Demidov, O. P.
Демидов, О. П.
The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide
description The action of 2,3-dimethylbenzothiazol-3-ium iodide on 1H-benzo[f]chromenes containing an acceptor substituent in the β-position to the oxygen atom in the presence of triethylamine results in the opening of the pyran ring and the formation of [(2E,4Z)-4-(3-methyl-benzothiazol-2(3H)-ylidene)but-2-en-1-yl]naphthalen-2-ols. In the case of 1-aryl-2-nitro-1H-benzo[f]chromenes, 3-methyl-2-[(1E,3Z)-3-(3-methylbenzothiazol-2(3H)-ylidene)prop-1-en-1-yl]benzothiazol-3-ium iodide was isolated. The resulting compounds containing the merocyanine chromophore are of interest as dyes and fluorescent labels.
format Статья
author Demidov, O. P.
Демидов, О. П.
author_facet Demidov, O. P.
Демидов, О. П.
author_sort Demidov, O. P.
title The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide
title_short The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide
title_full The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide
title_fullStr The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide
title_full_unstemmed The reactions of electron-deficient 1Н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide
title_sort reactions of electron-deficient 1н-benzo[f]chromenes with 2,3-dimethylbenzothiazol-3-ium iodide
publishDate 2023
url https://dspace.ncfu.ru/handle/20.500.12258/22265
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