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https://doi.org/10.2139/ssrn.4659364
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470147306.ch2openalex-extracted
Anomeric Effect: Origin and Consequences
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Targeting Oligosaccharides and Glycoconjugates Using Superselective Binding Scaffolds
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Recent Developments in Stereoselective Chemical Glycosylation
inferredcites →https://doi.org/10.1002/ajoc.202000558openalex-extracted
Influence of Remote Picolinyl and Picoloyl Stereodirecting Groups for the Stereoselective Glycosylation
inferredcites →https://doi.org/10.1002/anie.198602871openalex-extracted
Solvent Polarity and the Anomeric Effect
inferredcites →https://doi.org/10.1002/anie.200453688openalex-extracted
Mechanism of 4,6‐O‐Benzylidene‐Directed β‐Mannosylation as Determined by α‐Deuterium Kinetic Isotope Effects
inferredcites →https://doi.org/10.1002/anie.201411185openalex-extracted
The Problem of Origins and Origins of the Problem: Influence of Language on Studies Concerning the Anomeric Effect
inferredcites →https://doi.org/10.1002/anie.201907001openalex-extracted
Structural and Computational Analysis of 2‐Halogeno‐Glycosyl Cations in the Presence of a Superacid: An Expansive Platform
inferredcites →https://doi.org/10.1002/cctc.202200290openalex-extracted
Catalytic Radical Reactions of Unsaturated Sugars
inferredcites →https://doi.org/10.1002/ejoc.201402260openalex-extracted
Neighbouring Group Participation During Glycosylation: Do 2‐Substituted Ethyl Ethers Participate?
inferredcites →https://doi.org/10.1002/jcc.22885openalex-extracted
Multiwfn: A multifunctional wavefunction analyzer
inferredcites →https://doi.org/10.1002/qua.24757openalex-extracted
Intrinsic reaction coordinate: Calculation, bifurcation, and automated search
inferredcites →https://doi.org/10.1007/978-1-4614-8268-0openalex-extracted
Electrostatic and Stereoelectronic Effects in Carbohydrate Chemistry
inferredcites →https://doi.org/10.1007/978-3-642-68676-4openalex-extracted
The Anomeric Effect and Related Stereoelectronic Effects at Oxygen
inferredcites →https://doi.org/10.1007/s00214-007-0310-xopenalex-extracted
The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals
inferredcites →https://doi.org/10.1007/s00214-010-0846-zopenalex-extracted
Minimally augmented Karlsruhe basis sets
inferredcites →https://doi.org/10.1016/bs.accb.2022.10.005openalex-extracted
Conformationally restricted donors for stereoselective glycosylation
inferredcites →https://doi.org/10.1016/j.carres.2012.03.040openalex-extracted
Plausible transition states for glycosylation reactions
inferredcites →https://doi.org/10.1016/j.carres.2014.06.020openalex-extracted
A propos of glycosyl cations and the mechanism of chemical glycosylation; the current state of the art
inferredcites →https://doi.org/10.1016/j.carres.2014.10.013openalex-extracted
Contact ion pairs and solvent-separated ion pairs from d-mannopyranosyl and d-glucopyranosyl triflates
inferredcites →https://doi.org/10.1016/j.carres.2020.108045openalex-extracted
Chiral auxiliaries: Usefullness in stereoselective glycosylation reactions and their synthetic applications
inferredcites →https://doi.org/10.1016/j.carres.2022.108677openalex-extracted
Recent development of stereoselective C-glycosylation via generation of glycosyl radical
inferredcites →https://doi.org/10.1016/j.tifs.2020.11.027openalex-extracted
Preparation and biological activities of chitosan oligosaccharides
inferredcites →https://doi.org/10.1016/s0008-6215(02)00043-5openalex-extracted
Can the stereochemical outcome of glycosylation reactions be controlled by the conformational preferences of the glycosyl donor?
inferredcites →https://doi.org/10.1016/s0065-2318(09)00004-3openalex-extracted
Chapter 4 Computational Studies of the Role of Glycopyranosyl Oxacarbenium Ions in Glycobiology and Glycochemistry
inferredcites →https://doi.org/10.1021/acs.accounts.1c00021openalex-extracted
Glycosyl Oxocarbenium Ions: Structure, Conformation, Reactivity, and Interactions
inferredcites →https://doi.org/10.1021/acs.accounts.2c00040openalex-extracted
Characterization of Elusive Reaction Intermediates Using Infrared Ion Spectroscopy: Application to the Experimental Characterization of Glycosyl Cations
inferredcites →https://doi.org/10.1021/acs.chemrev.0c01210openalex-extracted
Discovery of Semi- and Fully-Synthetic Carbohydrate Vaccines Against Bacterial Infections Using a Medicinal Chemistry Approach
inferredcites →https://doi.org/10.1021/acs.chemrev.1c01032openalex-extracted
Glycoconjugates: Synthesis, Functional Studies, and Therapeutic Developments
inferredcites →https://doi.org/10.1021/acs.chemrev.2c00021openalex-extracted
Synthetic Glycans to Improve Current Glycoconjugate Vaccines and Fight Antimicrobial Resistance
inferredcites →https://doi.org/10.1021/acs.chemrev.5b00533openalex-extracted
Dispersion-Corrected Mean-Field Electronic Structure Methods
inferredcites →https://doi.org/10.1021/acs.chemrev.8b00083openalex-extracted
The Experimental Evidence in Support of Glycosylation Mechanisms at the SN1–SN2 Interface
inferredcites →https://doi.org/10.1021/acs.joc.8b00707openalex-extracted
The Anomeric Effect: It’s Complicated
inferredcites →https://doi.org/10.1021/acs.orglett.1c01218openalex-extracted
Convergent Palladium-Catalyzed Stereospecific Arginine Glycosylation Using Glycals
inferredcites →https://doi.org/10.1021/acs.orglett.1c04008openalex-extracted
Bismuth-Catalyzed Stereoselective 2-Deoxyglycosylation of Disarmed/Armed Glycal Donors
inferredcites →https://doi.org/10.1021/acs.orglett.3c01430openalex-extracted
α-Stereoselective 3-Deoxy- d -manno-oct-2-ulosonoic Acid (Kdo) O-Glycosylation with a p-Toluenethioglycoside Donor by the (p-Tol)2SO/Tf2O Preactivation Strategy
inferredcites →https://doi.org/10.1021/acs.orglett.9b00220openalex-extracted
1,2-trans Glycosylation via Neighboring Group Participation of 2-O-Alkoxymethyl Groups: Application to One-Pot Oligosaccharide Synthesis
inferredcites →https://doi.org/10.1021/acscatal.2c06308openalex-extracted
Reversible-Hydrogen-Transfer-Mediated Anomerization of Azaheterocyclyl 2-Deoxy-C-glycosides and Mechanistic Studies
inferredcites →https://doi.org/10.1021/acscatal.7b01630openalex-extracted
Catalyst-Controlled Stereoselective O-Glycosylation: Pd(0) vs Pd(II)
inferredcites →https://doi.org/10.1021/acscatal.9b00336openalex-extracted
Palladium-Catalyzed Stereospecific C -Glycosylation of Glycals with Vinylogous Acceptors
inferredcites →https://doi.org/10.1021/acscentsci.9b00042openalex-extracted
Defining the SN1 Side of Glycosylation Reactions: Stereoselectivity of Glycopyranosyl Cations
inferredcites →https://doi.org/10.1021/ar050189popenalex-extracted
Stereoelectronic Substituent Effects
inferredcites →https://doi.org/10.1021/ar100035ropenalex-extracted
Mechanism of a Chemical Glycosylation Reaction
inferredcites →https://doi.org/10.1021/bk-1993-0539openalex-extracted
The Anomeric Effect and Associated Stereoelectronic Effects
inferredcites →https://doi.org/10.1021/ct1001347openalex-extracted
Theoretical Investigation of Solvent Effects on Glycosylation Reactions: Stereoselectivity Controlled by Preferential Conformations of the Intermediate Oxacarbenium-Counterion Complex
inferredcites →https://doi.org/10.1021/ct200106aopenalex-extracted
Perspectives on Basis Sets Beautiful: Seasonal Plantings of Diffuse Basis Functions
inferredcites →https://doi.org/10.1021/ja011406uopenalex-extracted
Solid-Phase Synthesis of β-Mannosides
inferredcites →https://doi.org/10.1021/ja072440xopenalex-extracted
Electrochemical Generation of Glycosyl Triflate Pools
inferredcites →https://doi.org/10.1021/ja307266nopenalex-extracted
Cation Clock Permits Distinction Between the Mechanisms of α- and β-O- and β-C-Glycosylation in the Mannopyranose Series: Evidence for the Existence of a Mannopyranosyl Oxocarbenium Ion
inferredcites →https://doi.org/10.1021/ja971239ropenalex-extracted
Are Glycosyl Triflates Intermediates in the Sulfoxide Glycosylation Method? A Chemical and 1H, 13C, and 19F NMR Spectroscopic Investigation
inferredcites →https://doi.org/10.1021/ja9734814openalex-extracted
Direct Formation of β-Mannopyranosides and Other Hindered Glycosides from Thioglycosides
inferredcites →https://doi.org/10.1021/ja981041mopenalex-extracted
Exploring the Mechanism of Neighboring Group Assisted Glycosylation Reactions
inferredcites →https://doi.org/10.1021/jacs.0c05525openalex-extracted
Dissecting the Essential Role of Anomeric β-Triflates in Glycosylation Reactions
inferredcites →https://doi.org/10.1021/jacs.0c11106openalex-extracted
En Route to the Transformation of Glycoscience: A Chemist’s Perspective on Internal and External Crossroads in Glycochemistry
inferredcites →https://doi.org/10.1021/jacs.2c13018openalex-extracted
ortho -Methoxycarbonylethynylphenyl Thioglycosides (MCEPTs): Versatile Glycosyl Donors Enabled by Electron-Withdrawing Substituents and Catalyzed by Gold(I) or Cu(II) Complexes
inferredcites →https://doi.org/10.1021/jacs.7b09461openalex-extracted
Stereodirecting Effect of C5-Carboxylate Substituents on the Glycosylation Stereochemistry of 3-Deoxy- d -manno-oct-2-ulosonic Acid (Kdo) Thioglycoside Donors: Stereoselective Synthesis of α- and β-Kdo Glycosides
inferredcites →https://doi.org/10.1021/jacs.8b04525openalex-extracted
An Empirical Understanding of the Glycosylation Reaction
inferredcites →https://doi.org/10.1021/jacs.8b11005openalex-extracted
Oligosaccharide Synthesis and Translational Innovation
inferredcites →https://doi.org/10.1021/jo501012sopenalex-extracted
Theoretical Foundation for the Presence of Oxacarbenium Ions in Chemical Glycoside Synthesis
inferredcites →https://doi.org/10.1021/jo9606517openalex-extracted
Formation of β-Mannopyranosides of Primary Alcohols Using the Sulfoxide Method
inferredcites →https://doi.org/10.1021/jo962345zopenalex-extracted
Direct Synthesis of β-Mannopyranosides by the Sulfoxide Method
inferredcites →https://doi.org/10.1021/jp810292nopenalex-extracted
Universal Solvation Model Based on Solute Electron Density and on a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface Tensions
inferredcites →https://doi.org/10.1038/nchem.2399openalex-extracted
Catching elusive glycosyl cations in a condensed phase with HF/SbF5 superacid
inferredcites →https://doi.org/10.1038/nchem.721openalex-extracted
Computational evidence that hyperconjugative interactions are not responsible for the anomeric effect
inferredcites →https://doi.org/10.1038/s41467-020-16362-xopenalex-extracted
Characterization of glycosyl dioxolenium ions and their role in glycosylation reactions
inferredcites →https://doi.org/10.1039/9781788013864-00093openalex-extracted
Hydrogen-bond-mediated aglycone delivery (HAD) and related methods in carbohydrate chemistry
inferredcites →https://doi.org/10.1039/b508541aopenalex-extracted
Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy
inferredcites →https://doi.org/10.1039/c2ob06696copenalex-extracted
On a so-called “kinetic anomeric effect” in chemical glycosylation
inferredcites →https://doi.org/10.1039/c2ob26818copenalex-extracted
The anomeric effect: the dominance of exchange effects in closed-shell systems
inferredcites →https://doi.org/10.1039/c5ob00585jopenalex-extracted
The origin of the anomeric effect: probing the impacts of stereoelectronic interactions
inferredcites →https://doi.org/10.1039/c7cp04913gopenalex-extracted
A look at the density functional theory zoo with the advanced GMTKN55 database for general main group thermochemistry, kinetics and noncovalent interactions
inferredcites →https://doi.org/10.1039/d0ob02373fopenalex-extracted
Computational evidence of glycosyl cations
inferredcites →https://doi.org/10.1039/d0ob02453hopenalex-extracted
Probing the anomeric effect and mechanism of isomerization of oxazinane rings by DFT methods
inferredcites →https://doi.org/10.1039/d3ob00929gopenalex-extracted
Stereoselective oxidative O -glycosylation of disarmed glycosyl iodides with alcohols using PIDA as the promoter
inferredcites →https://doi.org/10.1055/s-1990-21214openalex-extracted
Nitriles as Solvents in Glycosylation Reactions: Highly Selective β-Glycoside Synthesis 1
inferredcites →https://doi.org/10.1063/1.3382344openalex-extracted
A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu
inferredcites →https://doi.org/10.1063/1.454172openalex-extracted
On evaluating the reaction path Hamiltonian
inferredcites →https://doi.org/10.1063/1.459634openalex-extracted
Following steepest descent reaction paths. The use of higher energy derivatives with a b i n i t i o electronic structure methods
inferredcites →https://doi.org/10.1063/1.463096openalex-extracted
Fully optimized contracted Gaussian basis sets for atoms Li to Kr
inferredcites →https://doi.org/10.1080/14760584.2019.1657012openalex-extracted
Glycoconjugate vaccines: current approaches towards faster vaccine design
inferredcites →https://doi.org/10.1134/s1068162021010258openalex-extracted
Protecting Groups as a Factor of Stereocontrol in Glycosylation Reactions
inferredcites →https://doi.org/10.1139/cjc-2016-0417openalex-extracted
Controlling the stereoselectivity of glycosylation via solvent effects
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