Synthesis of (1S,2S,3R,4R,5S)-methyl-3,5-di-O-benzyl-2-O-benzoyl-α-L-talofuranoside
- 作者: Khalikova M.J.1, Roziqov U.A.1, Skrylkova A.S.2, Egorov D.M.2, Safarov S.S.1
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隶属关系:
- V. I. Nikitin Institute of Chemistry, National Academy of Sciences of Tajikistan
- St. Petersburg State Institute of Technology (Technical University)
- 期: 卷 60, 编号 4 (2024)
- 页面: 516-522
- 栏目: Articles
- URL: https://ter-arkhiv.ru/0514-7492/article/view/672180
- DOI: https://doi.org/10.31857/S0514749224040137
- EDN: https://elibrary.ru/RYNANK
- ID: 672180
如何引用文章
详细
The article presents a method for the preparation of (1S,2S,3R,4R,5S)-methyl-3,5-di-O-benzyl-2-O-benzoyl-α-L-talofuranoside from (1S,2S,3R,4R,5S)-methyl-3,5-di-O-benzyl-1,2-O-isopropylidene-α-L-talofuranoside by successive treatment of the latter with a 20% solution of hydrochloric acid in aqueous methanol, followed by treatment with benzoyl chloride in dry pyridine. A promising use of methyl (1S,2S,3R,4R,5S)-3,5-di-O-benzyl-2-O-benzoyl-α-L-talofuranoside for the synthesis of new modified nucleosides after its acetylation has also been shown.
作者简介
M. Khalikova
V. I. Nikitin Institute of Chemistry, National Academy of Sciences of Tajikistan
Email: diavoly@mail.ru
塔吉克斯坦, ul. Ayni, 299/2, Dushanbe, 734063
U. Roziqov
V. I. Nikitin Institute of Chemistry, National Academy of Sciences of Tajikistan
Email: diavoly@mail.ru
塔吉克斯坦, ul. Ayni, 299/2, Dushanbe, 734063
A. Skrylkova
St. Petersburg State Institute of Technology (Technical University)
Email: diavoly@mail.ru
俄罗斯联邦, Moskovskii prosp., 26, St. Petersburg, 190013
D. Egorov
St. Petersburg State Institute of Technology (Technical University)
编辑信件的主要联系方式.
Email: diavoly@mail.ru
ORCID iD: 0000-0003-3744-9306
俄罗斯联邦, Moskovskii prosp., 26, St. Petersburg, 190013
S. Safarov
V. I. Nikitin Institute of Chemistry, National Academy of Sciences of Tajikistan
Email: diavoly@mail.ru
ORCID iD: 0000-0002-7193-6135
塔吉克斯坦, ul. Ayni, 299/2, Dushanbe, 734063
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