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First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof
C-glycopyranosyl derivatives of six-membered heterocycles are scarcely represented in the chemical literature and the title 3-glycopyranosyl-1,2,4-triazines are completely unknown. In this paper, the first synthesis of this compound class is accomplished by the cyclocondensation of C-glycosyl formam...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692545/ https://www.ncbi.nlm.nih.gov/pubmed/36431902 http://dx.doi.org/10.3390/molecules27227801 |
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author | Bokor, Éva Ferenczi, Attila Hashimov, Mahir Juhász-Tóth, Éva Götz, Zsófia Zaki, Alshimaa Ibrahim Somsák, László |
author_facet | Bokor, Éva Ferenczi, Attila Hashimov, Mahir Juhász-Tóth, Éva Götz, Zsófia Zaki, Alshimaa Ibrahim Somsák, László |
author_sort | Bokor, Éva |
collection | PubMed |
description | C-glycopyranosyl derivatives of six-membered heterocycles are scarcely represented in the chemical literature and the title 3-glycopyranosyl-1,2,4-triazines are completely unknown. In this paper, the first synthesis of this compound class is accomplished by the cyclocondensation of C-glycosyl formamidrazones and 1,2-dicarbonyl derivatives. In addition, the synthesis of C-glycopyranosyl 1,2,4-triazin-5(4H)-ones was also carried out by the transformation of the above formamidrazones with α-keto-carboxylic esters. Inverse electron demand Diels–Alder reactions of 3-glycopyranosyl-1,2,4-triazines with a bicyclononyne derivative yielded the corresponding annulated 2-glycopyranosyl pyridines. |
format | Online Article Text |
id | pubmed-9692545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96925452022-11-26 First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof Bokor, Éva Ferenczi, Attila Hashimov, Mahir Juhász-Tóth, Éva Götz, Zsófia Zaki, Alshimaa Ibrahim Somsák, László Molecules Article C-glycopyranosyl derivatives of six-membered heterocycles are scarcely represented in the chemical literature and the title 3-glycopyranosyl-1,2,4-triazines are completely unknown. In this paper, the first synthesis of this compound class is accomplished by the cyclocondensation of C-glycosyl formamidrazones and 1,2-dicarbonyl derivatives. In addition, the synthesis of C-glycopyranosyl 1,2,4-triazin-5(4H)-ones was also carried out by the transformation of the above formamidrazones with α-keto-carboxylic esters. Inverse electron demand Diels–Alder reactions of 3-glycopyranosyl-1,2,4-triazines with a bicyclononyne derivative yielded the corresponding annulated 2-glycopyranosyl pyridines. MDPI 2022-11-12 /pmc/articles/PMC9692545/ /pubmed/36431902 http://dx.doi.org/10.3390/molecules27227801 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bokor, Éva Ferenczi, Attila Hashimov, Mahir Juhász-Tóth, Éva Götz, Zsófia Zaki, Alshimaa Ibrahim Somsák, László First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof |
title | First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof |
title_full | First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof |
title_fullStr | First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof |
title_full_unstemmed | First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof |
title_short | First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions Thereof |
title_sort | first synthesis of 3-glycopyranosyl-1,2,4-triazines and some cycloadditions thereof |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692545/ https://www.ncbi.nlm.nih.gov/pubmed/36431902 http://dx.doi.org/10.3390/molecules27227801 |
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