Pyranoside-into-furanoside rearrangement of D-glucuronopyranoside derivatives

Pyranoside-into-furanoside rearrangement of D-glucuronopyranoside derivatives Full article

Journal

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

Output data

Year: 2016, Volume: 26, Number: 6, Pages: 483-484 Pages count : 2 DOI: 10.1016/j.mencom.2016.11.007

Authors

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

Affiliations

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

The pyranoside-into-furanoside (PIF) rearrangement of α and β-d-glucuronopyranosides under acid-promoted sulfation proceeded significantly faster than similar isomerization of β-d-glucopyranosides.

Krylov V.B. , Argunov D.A. , Nifantiev N.E.
Pyranoside-into-furanoside rearrangement of D-glucuronopyranoside derivatives
Mendeleev Communications. 2016. V.26. N6. P.483-484. DOI: 10.1016/j.mencom.2016.11.007 WOS Scopus OpenAlex

≡ Web of science:	WOS:000390515200007
≡ Scopus:	2-s2.0-84997218102
≡ OpenAlex:	W2553175593