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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...

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Detalles Bibliográficos
Autores principales: Kazakova, O. B., Giniyatullina, G. V., Tolstikov, G. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SP MAIK Nauka/Interperiodica 2011
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.
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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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