The synthesis of thioglucoside and their tetracyclic conjugate based on 6-bromo-1,4-naphthoquinone
- Authors: Polonik S.G1, Popov R.S1, Makhankov V.V1, Sabutskii Y.E1
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Affiliations:
- G.B. Elyakov Pacific Insitute Bioorganic Chemistry Far East Branch Russian Academy of Sciences
- Issue: Vol 59, No 4 (2023)
- Pages: 444-453
- Section: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/144748
- DOI: https://doi.org/10.31857/S0514749223040031
- EDN: https://elibrary.ru/AQWZMD
- ID: 144748
Cite item
Abstract
A bromine-containing naphthoquinone-carbohydrate conjugate was obtained for the first time by intramolecular condensation of 3-acetylthioglucoside of 6-bromo-2-methoxy-1,4-naphthoquinone under sodium methoxide/ methanol treatment. It has been established that the heterocyclization reaction is accompanied by the substitution of the thioglucoside substituent by the methoxyl group and the formation of an isomeric conjugate.
About the authors
S. G Polonik
G.B. Elyakov Pacific Insitute Bioorganic Chemistry Far East Branch Russian Academy of Sciences
Email: sergpol@piboc.dvo.ru
R. S Popov
G.B. Elyakov Pacific Insitute Bioorganic Chemistry Far East Branch Russian Academy of Sciences
Email: sergpol@piboc.dvo.ru
V. V Makhankov
G.B. Elyakov Pacific Insitute Bioorganic Chemistry Far East Branch Russian Academy of Sciences
Email: sergpol@piboc.dvo.ru
Y. E Sabutskii
G.B. Elyakov Pacific Insitute Bioorganic Chemistry Far East Branch Russian Academy of Sciences
Email: sergpol@piboc.dvo.ru
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