Abstract:
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.
Document Type:
Article
Language: English
Citation:
V. B. Krylov, D. A. Argunov, N. E. Nifantiev, “Pyranoside-into-furanoside rearrangement of D-glucuronopyranoside derivatives”, Mendeleev Commun., 26:6 (2016), 483–484
Linking options:
https://www.mathnet.ru/eng/mendc2253
https://www.mathnet.ru/eng/mendc/v26/i6/p483
This publication is cited in the following 1 articles:
A. N. Vereshchagin, “Classical and interdisciplinary approaches to the design of organic and hybrid molecular systems”, Russ Chem Bull, 66:10 (2017), 1765
Contact us: