Driving Force of the Pyranoside-into-Furanoside Rearrangement-Reference-Cited by-同舟云学术

Driving Force of the Pyranoside-into-Furanoside Rearrangement

Published:2019-01-14 Issue:1 Volume:4 Page:1139-1143
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Gerbst Alexey G.¹,Krylov Vadim B.¹,Argunov Dmitry A.¹,Dmitrenok Andrey S.¹,Nifantiev Nikolay E.¹^ORCID

Affiliation:

1. Laboratory of Glycoconjugate Chemistry, N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect 47, 119991 Moscow, Russia

Funder

Russian Science Foundation

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.8b03274

Reference24 articles.

1. PYRANOSE–FURANOSE AND ANOMERIC EQUILIBRIA: INFLUENCE OF SOLVENT AND OF PARTIAL METHYLATION

2. Glycosidation of sugars. IV. Methanolysis of D-glucose, D-galactose, and D-mannose

3. GLYCOSIDATION OF SUGARS: I. FORMATION OF METHYL-D-XYLOSIDES

4. Synthesis of 6′-Aminohexyl 2-Acetamido-2-deoxy-D-galactoside Isomers and a Unique Isomerization Catalyzed by Ion Exchange Resin

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Acid-Catalyzed Transformation of Pyranosides into Furanosides as a Tool for Preparation of Furanoside Synthetic Blocks;Organic Letters;2024-09-13

2. Unveiling the role of the ring size in the sugar-based tensides surfactancy by interfacial studies and molecular dynamics;Journal of Molecular Liquids;2024-08

3. Synthesis and ab initio conformational investigation of a series of model sulfated α-L-iduronopyranosides;Carbohydrate Research;2024-04

4. Computational and NMR Conformational Analysis of Galactofuranoside Cycles Presented in Bacterial and Fungal Polysaccharide Antigens;Frontiers in Molecular Biosciences;2021-08-25

5. A Rapid and Mild Sulfation Strategy Reveals Conformational Preferences in Therapeutically Relevant Sulfated Xylooligosaccharides;Chemistry – A European Journal;2021-05-28