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Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids
New potentially biologically active sulfonamide derivatives of pentacyclic lupane-type triterpenoids, the sulfonamide group of which was bonded to C-17 of the triterpene skeleton through an amidoethane spacer, were synthesized via conjugation of 2-aminoethanesulfonamides to betulinic and betulonic a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275633/ https://www.ncbi.nlm.nih.gov/pubmed/34276060 http://dx.doi.org/10.1007/s10600-021-03455-2 |
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author | Komissarova, N. G. Dubovitskii, S. N. Shitikova, O. V. Orlov, A. V. |
author_facet | Komissarova, N. G. Dubovitskii, S. N. Shitikova, O. V. Orlov, A. V. |
author_sort | Komissarova, N. G. |
collection | PubMed |
description | New potentially biologically active sulfonamide derivatives of pentacyclic lupane-type triterpenoids, the sulfonamide group of which was bonded to C-17 of the triterpene skeleton through an amidoethane spacer, were synthesized via conjugation of 2-aminoethanesulfonamides to betulinic and betulonic acids in the presence of Mukaiyama reagent (2-bromo-1-methylpyridinium iodide). |
format | Online Article Text |
id | pubmed-8275633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-82756332021-07-14 Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids Komissarova, N. G. Dubovitskii, S. N. Shitikova, O. V. Orlov, A. V. Chem Nat Compd Article New potentially biologically active sulfonamide derivatives of pentacyclic lupane-type triterpenoids, the sulfonamide group of which was bonded to C-17 of the triterpene skeleton through an amidoethane spacer, were synthesized via conjugation of 2-aminoethanesulfonamides to betulinic and betulonic acids in the presence of Mukaiyama reagent (2-bromo-1-methylpyridinium iodide). Springer US 2021-07-13 2021 /pmc/articles/PMC8275633/ /pubmed/34276060 http://dx.doi.org/10.1007/s10600-021-03455-2 Text en © Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Komissarova, N. G. Dubovitskii, S. N. Shitikova, O. V. Orlov, A. V. Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids |
title | Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids |
title_full | Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids |
title_fullStr | Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids |
title_full_unstemmed | Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids |
title_short | Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids |
title_sort | synthesis of 2-aminoethanesulfonamides of betulinic and betulonic acids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275633/ https://www.ncbi.nlm.nih.gov/pubmed/34276060 http://dx.doi.org/10.1007/s10600-021-03455-2 |
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