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Synthesis of berberine bromide analogs containing tertiary amides of acetic acid in the 9-O-position Full article

Journal Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388
Output data Year: 2013, Volume: 48, Number: 6, Pages: 1047-1053 Pages count : DOI: 10.1007/s10600-013-0461-z
Tags berberine; berberine chloride; berberrubine; tertiary amides; isoquinoline alkaloids; hypocholesterolemic activity
Authors Nechepurenko I. V. 1 , Komarova N. I. 1 , Vasil'ev V. G. 1 , Salakhutdinov N. F. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, N N Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: 9-O-Acetamide analogs of berberine bromide were prepared in 20-87% yields via reaction of the isoquinoline alkaloid berberrubine with tertiary amides of bromoacetic acid. Aminolysis did not occur during reaction of methyl-2-(9-demethoxyberberine bromide-9-yl)hydroxyacetate with secondary amines. The corresponding acid or its ethyl ester was isolated.
Cite: Nechepurenko I.V. , Komarova N.I. , Vasil'ev V.G. , Salakhutdinov N.F.
Synthesis of berberine bromide analogs containing tertiary amides of acetic acid in the 9-O-position
Chemistry of Natural Compounds. 2013. V.48. N6. P.1047-1053. DOI: 10.1007/s10600-013-0461-z WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Jan 1, 2013
Published online: Feb 22, 2013
Identifiers:
Web of science: WOS:000315417600033
Scopus: 2-s2.0-84874403842
Elibrary: 24941697
OpenAlex: W1967868005
Citing:
DB Citing
Web of science 8
Scopus 9
Elibrary 8
OpenAlex 9
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