Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides

Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides Научная публикация

Журнал

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Вых. Данные

Год: 1998, Том: 8, Номер: 1, Страницы: 9-11 Страниц : 3 DOI: 10.1070/mc1998v008n01abeh000887

Авторы

Sherman Andrei A. ¹ , Kononov Leonid O. ¹ , Shashkov Alexander S. ¹ , Zatonsky Georgij V. ¹ , Nifant’ev Nikolay E. ¹

Организации

1	N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow, Russian Federation

Protected 3-aminopropyl spacer-armed glycosides that can be further used for the preparation of neoglycoconjugates have been prepared from allyl glycosides using azidophenylselenylation of the double bond as a key step.

Sherman A.A. , Kononov L.O. , Shashkov A.S. , Zatonsky G.V. , Nifant’ev N.E.
Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides
Mendeleev Communications. 1998. V.8. N1. P.9-11. DOI: 10.1070/mc1998v008n01abeh000887 Scopus OpenAlex

Scopus:	2-s2.0-26144458392
OpenAlex:	W2042702775

БД	Цитирований
OpenAlex	9
Scopus	11