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Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids
Development of the functionalization of triterpenoids to A-secoamidoximes, A-secomethylenamines, and branched 3-(3-aminopropylamino)-3-(3-aminopropoxy)amidoximes is illustrated by the betulonic acid ketoxime. An effective way to get of the derivatives of 20,29-dihydrolupanes using diborane is sugges...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SP MAIK Nauka/Interperiodica
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088524/ https://www.ncbi.nlm.nih.gov/pubmed/22332366 http://dx.doi.org/10.1134/S1068162011050086 |
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author | Kazakova, O. B. Giniyatullina, G. V. Tolstikov, G. A. |
author_facet | Kazakova, O. B. Giniyatullina, G. V. Tolstikov, G. A. |
author_sort | Kazakova, O. B. |
collection | PubMed |
description | Development of the functionalization of triterpenoids to A-secoamidoximes, A-secomethylenamines, and branched 3-(3-aminopropylamino)-3-(3-aminopropoxy)amidoximes is illustrated by the betulonic acid ketoxime. An effective way to get of the derivatives of 20,29-dihydrolupanes using diborane is suggested. The antiviral and antituberculosis activity data of some compounds are presented. |
format | Online Article Text |
id | pubmed-7088524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | SP MAIK Nauka/Interperiodica |
record_format | MEDLINE/PubMed |
spelling | pubmed-70885242020-03-23 Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids Kazakova, O. B. Giniyatullina, G. V. Tolstikov, G. A. Russ J Bioorgan Chem Article Development of the functionalization of triterpenoids to A-secoamidoximes, A-secomethylenamines, and branched 3-(3-aminopropylamino)-3-(3-aminopropoxy)amidoximes is illustrated by the betulonic acid ketoxime. An effective way to get of the derivatives of 20,29-dihydrolupanes using diborane is suggested. The antiviral and antituberculosis activity data of some compounds are presented. SP MAIK Nauka/Interperiodica 2011-10-01 2011 /pmc/articles/PMC7088524/ /pubmed/22332366 http://dx.doi.org/10.1134/S1068162011050086 Text en © Pleiades Publishing, Ltd. 2011 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 Kazakova, O. B. Giniyatullina, G. V. Tolstikov, G. A. Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids |
title | Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids |
title_full | Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids |
title_fullStr | Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids |
title_full_unstemmed | Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids |
title_short | Synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids |
title_sort | synthesis of a-secomethylenamino- and substituted amidoximotriterpenoids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088524/ https://www.ncbi.nlm.nih.gov/pubmed/22332366 http://dx.doi.org/10.1134/S1068162011050086 |
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