Sciact
  • EN
  • RU

Synthesis of hexaarabinofuranoside bearing the 4-(3-azidopropoxy)phenyl aglycone related to the terminal fragment of polysaccharides of mycobacteria Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2024, Том: 73, Номер: 5, Страницы: 1417-1425 Страниц : 9 DOI: 10.1007/s11172-024-4260-4
Авторы Abronina P.I. 1 , Malysheva N.N. 1 , Zinin A.I. 1 , Kolotyrkina N.G. 1 , Kononov L.O. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

Реферат: A convergent synthesis α-(1→3)-, α-(1→5), β-(1→2)-linked hexaarabinofuranoside related to the terminal fragment of lipoarabinomannan (LAM) and arabinogalactan of mycobacteria as a glycoside with 4-(3-azidopropoxy)phenyl aglycone was accomplished. 4-(3-Azidopropoxy)phenyl aglycone belongs to the class of Janus aglycones, which can be used as both a temporary protective group for the anomeric position of the carbohydrate and a (pre)spacer for the synthesis of neoglycoconjugates. The key step of the synthesis is the formation of 1,2-trans glycosidic linkage with the use of Ara-β-(1→2)-Ara p-tolylthioarabinofuranoside bearing five triisopropylsilyl groups.
Библиографическая ссылка: Abronina P.I. , Malysheva N.N. , Zinin A.I. , Kolotyrkina N.G. , Kononov L.O.
Synthesis of hexaarabinofuranoside bearing the 4-(3-azidopropoxy)phenyl aglycone related to the terminal fragment of polysaccharides of mycobacteria
Russian Chemical Bulletin. 2024. V.73. N5. P.1417-1425. DOI: 10.1007/s11172-024-4260-4 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001252371600005
Scopus: 2-s2.0-85196618127
OpenAlex: W4399899308
Цитирование в БД:
БД Цитирований
OpenAlex 4
Scopus 4
Web of science 4
Альметрики: