Synthesis of (1S,2S,3R,4R,5S)-methyl-3,5-di-O-benzyl-2-O-benzoyl-α-L-talofuranoside
- Autores: Khalikova M.J.1, Roziqov U.A.1, Skrylkova A.S.2, Egorov D.M.2, Safarov S.S.1
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Afiliações:
- V. I. Nikitin Institute of Chemistry, National Academy of Sciences of Tajikistan
- St. Petersburg State Institute of Technology (Technical University)
- Edição: Volume 60, Nº 4 (2024)
- Páginas: 516-522
- Seção: Articles
- URL: https://transsyst.ru/0514-7492/article/view/672180
- DOI: https://doi.org/10.31857/S0514749224040137
- EDN: https://elibrary.ru/RYNANK
- ID: 672180
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Resumo
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.
Sobre autores
M. Khalikova
V. I. Nikitin Institute of Chemistry, National Academy of Sciences of Tajikistan
Email: diavoly@mail.ru
Tajiquistão, ul. Ayni, 299/2, Dushanbe, 734063
U. Roziqov
V. I. Nikitin Institute of Chemistry, National Academy of Sciences of Tajikistan
Email: diavoly@mail.ru
Tajiquistão, ul. Ayni, 299/2, Dushanbe, 734063
A. Skrylkova
St. Petersburg State Institute of Technology (Technical University)
Email: diavoly@mail.ru
Rússia, Moskovskii prosp., 26, St. Petersburg, 190013
D. Egorov
St. Petersburg State Institute of Technology (Technical University)
Autor responsável pela correspondência
Email: diavoly@mail.ru
ORCID ID: 0000-0003-3744-9306
Rússia, 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
Tajiquistão, ul. Ayni, 299/2, Dushanbe, 734063
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