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Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups
The first synthesis of 5,12-diamino-7,14-bis(aryl)-1,4,8,11-tetrathiacyclotetradeca-5,12-diene-6,13-dicarbonitriles was performed as a multicomponent macroheterocyclization of malononitrile, aryl aldehydes, and 1,2-ethanedithiol in the presence of a catalytic amount of triethylamine in ethanol. The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033490/ https://www.ncbi.nlm.nih.gov/pubmed/35478647 http://dx.doi.org/10.1039/d1ra02616j |
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author | Akhmadiev, Nail S. Mescheryakova, Ekaterina S. Akhmetova, Vnira R. Ibragimov, Askhat G. |
author_facet | Akhmadiev, Nail S. Mescheryakova, Ekaterina S. Akhmetova, Vnira R. Ibragimov, Askhat G. |
author_sort | Akhmadiev, Nail S. |
collection | PubMed |
description | The first synthesis of 5,12-diamino-7,14-bis(aryl)-1,4,8,11-tetrathiacyclotetradeca-5,12-diene-6,13-dicarbonitriles was performed as a multicomponent macroheterocyclization of malononitrile, aryl aldehydes, and 1,2-ethanedithiol in the presence of a catalytic amount of triethylamine in ethanol. The structures of the obtained macroheterocycles were confirmed by spectral methods, X-ray diffraction, and MALDI TOF mass spectrometry. |
format | Online Article Text |
id | pubmed-9033490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90334902022-04-26 Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups Akhmadiev, Nail S. Mescheryakova, Ekaterina S. Akhmetova, Vnira R. Ibragimov, Askhat G. RSC Adv Chemistry The first synthesis of 5,12-diamino-7,14-bis(aryl)-1,4,8,11-tetrathiacyclotetradeca-5,12-diene-6,13-dicarbonitriles was performed as a multicomponent macroheterocyclization of malononitrile, aryl aldehydes, and 1,2-ethanedithiol in the presence of a catalytic amount of triethylamine in ethanol. The structures of the obtained macroheterocycles were confirmed by spectral methods, X-ray diffraction, and MALDI TOF mass spectrometry. The Royal Society of Chemistry 2021-05-25 /pmc/articles/PMC9033490/ /pubmed/35478647 http://dx.doi.org/10.1039/d1ra02616j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Akhmadiev, Nail S. Mescheryakova, Ekaterina S. Akhmetova, Vnira R. Ibragimov, Askhat G. Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups |
title | Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups |
title_full | Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups |
title_fullStr | Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups |
title_full_unstemmed | Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups |
title_short | Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups |
title_sort | metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033490/ https://www.ncbi.nlm.nih.gov/pubmed/35478647 http://dx.doi.org/10.1039/d1ra02616j |
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