Characterization of glycosyl dioxolenium ions and their role in glycosylation reactions
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Title
Characterization of glycosyl dioxolenium ions and their role in glycosylation reactions
Authors
Keywords
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Journal
Nature Communications
Volume 11, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-05-29
DOI
10.1038/s41467-020-16362-x
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Note: Only part of the references are listed.- Remote Participation during Glycosylation Reactions of Galactose Building Blocks: Direct Evidence from Cryogenic Vibrational Spectroscopy
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- Synthesis, Reactivity, and Stereoselectivity of 4-Thiofuranosides
- (2019) Jerre M. Madern et al. JOURNAL OF ORGANIC CHEMISTRY
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- (2019) Hidde Elferink et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Furanosyl Oxocarbenium Ion Conformational Energy Landscape Maps as a Tool to Study the Glycosylation Stereoselectivity of 2‐Azidofuranoses, 2‐Fluorofuranoses and Methyl Furanosyl Uronates
- (2019) Stefan van der Vorm et al. CHEMISTRY-A EUROPEAN JOURNAL
- Defining the SN1 Side of Glycosylation Reactions: Stereoselectivity of Glycopyranosyl Cations
- (2019) Thomas Hansen et al. ACS Central Science
- Structural and Computational Analysis of 2-Halogeno-Glycosyl Cations in Superacid: An extansive Platform
- (2019) Ludivine Lebedel et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Stereodirecting Effect of C3-Ester Groups on the Glycosylation Stereochemistry of L-Rhamnopyranose Thioglycoside Donors: Stereoselective Synthesis of α- and β-L-Rhamnopyranosides
- (2019) Jin-Cai Lei et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Establishment of Guidelines for the Control of Glycosylation Reactions and Intermediates by Quantitative Assessment of Reactivity
- (2019) Chun-Wei Chang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Dual-Participation Protecting Group Solves the Anomeric Stereocontrol Problems in Glycosylation Reactions
- (2019) Hui Liu et al. ORGANIC LETTERS
- Venturing beyond Donor-Controlled Glycosylation: New Perspectives toward Anomeric Selectivity
- (2018) Wei-Lin Leng et al. ACCOUNTS OF CHEMICAL RESEARCH
- Direct Experimental Characterization of Glycosyl Cations by Infrared Ion Spectroscopy
- (2018) Hidde Elferink et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Structural absorption by barbule microstructures of super black bird of paradise feathers
- (2018) Dakota E. McCoy et al. Nature Communications
- Mapping the Reactivity and Selectivity of 2-Azidofucosyl Donors for the Assembly of N-Acetylfucosamine-Containing Bacterial Oligosaccharides
- (2017) Bas Hagen et al. JOURNAL OF ORGANIC CHEMISTRY
- The influence of acceptor nucleophilicity on the glycosylation reaction mechanism
- (2017) S. van der Vorm et al. Chemical Science
- In situ click chemistry generation of cyclooxygenase-2 inhibitors
- (2017) Atul Bhardwaj et al. Nature Communications
- Infrared ion spectroscopy in a modified quadrupole ion trap mass spectrometer at the FELIX free electron laser laboratory
- (2016) Jonathan Martens et al. REVIEW OF SCIENTIFIC INSTRUMENTS
- A propos of glycosyl cations and the mechanism of chemical glycosylation; the current state of the art
- (2015) Luis Bohé et al. CARBOHYDRATE RESEARCH
- Mechanisms of Glycosylation Reactions Studied by Low-Temperature Nuclear Magnetic Resonance
- (2015) Tobias Gylling Frihed et al. CHEMICAL REVIEWS
- Catching elusive glycosyl cations in a condensed phase with HF/SbF5 superacid
- (2015) A. Martin et al. Nature Chemistry
- Directing effect by remote electron-withdrawing protecting groups at O-3 or O-4 position of donors in glucosylations and galactosylations
- (2015) Ju Yuel Baek et al. TETRAHEDRON
- Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry
- (2015) Swati S. Nigudkar et al. Chemical Science
- Furanosyl Oxocarbenium Ion Stability and Stereoselectivity
- (2014) Erwin R. van Rijssel et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Bringing the MMFF force field to the RDKit: implementation and validation
- (2014) Paolo Tosco et al. Journal of Cheminformatics
- Is an acyl group at O-3 in glucosyl donors able to control α-stereoselectivity of glycosylation? The role of conformational mobility and the protecting group at O-6
- (2013) Bozhena S. Komarova et al. CARBOHYDRATE RESEARCH
- Identification of 3,6-di-O-acetyl-1,2,4-O-orthoacetyl-α-d-glucopyranose as a direct evidence for the 4-O-acyl group participation in glycosylation
- (2011) Yuyong Ma et al. CHEMICAL COMMUNICATIONS
- Use of Solution-Phase Vibrational Frequencies in Continuum Models for the Free Energy of Solvation
- (2011) Raphael F. Ribeiro et al. JOURNAL OF PHYSICAL CHEMISTRY B
- New Principles for Glycoside-Bond Formation
- (2009) Xiangming Zhu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- β-Directing Effect of Electron-Withdrawing Groups atO-3,O-4, andO-6 Positions and α-Directing Effect by Remote Participation of 3-O-Acyl and 6-O-Acetyl Groups of Donors in Mannopyranosylations
- (2009) Ju Yuel Baek et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Does Neighboring Group Participation by Non-Vicinal Esters Play a Role in Glycosylation Reactions? Effective Probes for the Detection of Bridging Intermediates
- (2008) David Crich et al. JOURNAL OF ORGANIC CHEMISTRY
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