Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives

Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives Научная публикация

Журнал

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

Вых. Данные

Год: 2014, Том: 24, Номер: 6, Страницы: 336-337 Страниц : 2 DOI: 10.1016/j.mencom.2014.11.006

Авторы

Krylov Vadim B. ¹ , Argunov Dmitry A. ¹ , Nifantiev Nikolay E. ¹

Организации

1	N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991,Moscow, Russian Federation

Heating of trisodium salt of allyl 3-O-benzyl-2,5,6-tri-O-sulfonato-β-D-galactofuranoside with pyridinium chloride in dioxane affords 1,6-anhydro-3-O-benzyl-α-D-galactofuranose which was regioselectively acylated to give useful precursors for oligosaccharide synthesis.

Krylov V.B. , Argunov D.A. , Nifantiev N.E.
Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives
Mendeleev Communications. 2014. V.24. N6. P.336-337. DOI: 10.1016/j.mencom.2014.11.006 WOS Scopus OpenAlex

≡ Web of science:	WOS:000347139100006
≡ Scopus:	2-s2.0-84911935133
≡ OpenAlex:	W1996452709