Sciact
  • EN
  • RU

Smiles rearrangements in a series of berberine analogues containing a secondary acetamide fragment Full article

Journal Tetrahedron Letters
ISSN: 0040-4039
Output data Year: 2014, Volume: 55, Number: 44, Pages: 6125-6127 Pages count : DOI: 10.1016/j.tetlet.2014.09.059
Tags Smiles rearrangement; Berberine; Berberrubine; Secondary amides; Isoquinoline alkaloids
Authors Nechepurenko Ivan V. 1 , Komarova Nina I. 1 , Shernyukov Andrey V. 1 , Vasiliev Vladimir G. 1 , Salakhutdinov Nariman F. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, NN Vorozhtzov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: Smiles rearrangements occurring in the derivatives of the isoquinoline alkaloid, berberine, containing an oxyacetic acid fragment at C-9 are described. Methyl-2-(9-demethoxyberberinebromide-9-yl)oxyacetate reacts with an excess of propylamine followed by sequential aminolysis and Smiles rearrangement leading to 2-hydroxy-N-(berbero-9-yl)-N-propylacetamide in 80% yield. Reactions of berberrubine with secondary amides of bromoacetic acid via Smiles rearrangement give N-substituted 2-hydroxy-N-(berbero-9-yl)acetamides (yields 20-36%). In some cases, the intermediate secondary amides were isolated. (C) 2014 Elsevier Ltd. All rights reserved.
Cite: Nechepurenko I.V. , Komarova N.I. , Shernyukov A.V. , Vasiliev V.G. , Salakhutdinov N.F.
Smiles rearrangements in a series of berberine analogues containing a secondary acetamide fragment
Tetrahedron Letters. 2014. V.55. N44. P.6125-6127. DOI: 10.1016/j.tetlet.2014.09.059 WOS Scopus OpenAlex
Dates:
Published print: Oct 1, 2014
Identifiers:
Web of science: WOS:000343625300026
Scopus: 2-s2.0-84949143646
OpenAlex: W2086439094
Citing:
DB Citing
Web of science 5
Scopus 7
OpenAlex 7
Altmetrics: