Acetylenic derivatives of betulonic acid amide as a new type of compounds possessing spasmolytic activity Full article
Journal |
Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171 |
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Output data | Year: 2015, Volume: 64, Number: 6, Pages: 1327-1334 Pages count : DOI: 10.1007/s11172-015-1013-4 | ||||||||
Tags | triterpenoids; betulonic acid; acetylenes; azides; Mannich bases; 1,3-dipolar cycloadditions; anti-inflammatory activity; hepatoprotective activity; spasmolytic activity | ||||||||
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Abstract:
Efficient and versatile synthetic procedures towards novel derivatives of betulonic acid via Mannich reaction, Sonogashira cross-coupling, and copper(i)-catalyzed 1,3-dipolar cyclo-additions were developed. Introduction of secondary amines (Mannich reaction) into betulonic acid amides led to derivatives possessing marked spasmolytic activity, which is not characteristic of the triterpene fragment.
Cite:
Govdi A.I.
, Sorokina I.V.
, Baev D.S.
, Bryzgalov A.O.
, Tolstikova T.G.
, Tolstikov G.A.
, Vasilevsky S.F.
Acetylenic derivatives of betulonic acid amide as a new type of compounds possessing spasmolytic activity
Russian Chemical Bulletin. 2015. V.64. N6. P.1327-1334. DOI: 10.1007/s11172-015-1013-4 WOS Scopus РИНЦ
Acetylenic derivatives of betulonic acid amide as a new type of compounds possessing spasmolytic activity
Russian Chemical Bulletin. 2015. V.64. N6. P.1327-1334. DOI: 10.1007/s11172-015-1013-4 WOS Scopus РИНЦ
ArticleLinkType.TRANSLATED_TO_ORIGINAL:
Говди А.И.
, Сорокина И.В.
, Баев Д.С.
, Брызгалов А.О.
, Толстикова Т.Г.
, Толстиков Г.А.
, Василевский С.Ф.
Ацетиленовые производные амида бетулоновой кислоты - новая группа соединений, обладающих спазмолитической активностью
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2015. №6. С.1327. РИНЦ
Ацетиленовые производные амида бетулоновой кислоты - новая группа соединений, обладающих спазмолитической активностью
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2015. №6. С.1327. РИНЦ
Dates:
Published print: | Jun 1, 2015 |
Published online: | Feb 27, 2016 |
Identifiers:
Web of science | WOS:000371313900010 |
Scopus | 2-s2.0-84959375742 |
Elibrary | 26972304 |
OpenAlex | W2341307749 |