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Theoretical Foundation for the Presence of Oxacarbenium Ions in Chemical Glycoside Synthesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200802036openalex-snapshot
New Principles for Glycoside‐Bond Formation
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Ueber einige Derivate des Traubenzuckers und der Galactose
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Anomeric distinction and oxonium ion formation in acetylated glycosides
inferredcites →https://doi.org/10.1002/jms.880openalex-snapshot
Formation and stability of oxocarbenium ions from glycosides
inferredcites →https://doi.org/10.1007/s00214-007-0310-xopenalex-snapshot
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/10.1016/j.carres.2004.12.021openalex-snapshot
The two-conformer hypothesis: 2,3,4,6-tetra-O-methyl-mannopyranosyl and -glucopyranosyl oxacarbenium ions
inferredcites →https://doi.org/10.1016/j.carres.2006.09.027openalex-snapshot
Investigations into the role of oxacarbenium ions in glycosylation reactions by ab initio molecular dynamics
inferredcites →https://doi.org/10.1016/j.carres.2007.05.012openalex-snapshot
DFT studies of the ionization of alpha and beta glycopyranosyl donors
inferredcites →https://doi.org/10.1016/j.carres.2007.09.007openalex-snapshot
O-2 Substituted pyranosyl oxacarbenium ions are C-2–O-2 2-fold rotors with a strong syn preference
inferredcites →https://doi.org/10.1016/j.carres.2010.02.027openalex-snapshot
The impact of oxacarbenium ion conformers on the stereochemical outcome of glycosylations
inferredcites →https://doi.org/10.1016/j.carres.2010.06.004openalex-snapshot
Computational study of the influence of cyclic protecting groups in stereoselectivity of glycosylation reactions
inferredcites →https://doi.org/10.1016/j.carres.2012.03.040openalex-snapshot
Plausible transition states for glycosylation reactions
inferredcites →https://doi.org/10.1016/j.carres.2012.04.001openalex-snapshot
Complications of modeling glycosylation reactions: can the anomeric conformation of a donor determine the glycopyranosyl oxacarbenium ring conformation?
inferredcites →https://doi.org/10.1016/s0008-6215(02)00043-5openalex-snapshot
Can the stereochemical outcome of glycosylation reactions be controlled by the conformational preferences of the glycosyl donor?
inferredcites →https://doi.org/10.1021/ar100035ropenalex-snapshot
Mechanism of a Chemical Glycosylation Reaction
inferredcites →https://doi.org/10.1021/ct1001347openalex-snapshot
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/ct800568mopenalex-snapshot
The DBH24/08 Database and Its Use to Assess Electronic Structure Model Chemistries for Chemical Reaction Barrier Heights
inferredcites →https://doi.org/10.1021/ja00839a011openalex-snapshot
General definition of ring puckering coordinates
inferredcites →https://doi.org/10.1021/ja00847a032openalex-snapshot
Halide ion catalyzed glycosidation reactions. Syntheses of .alpha.-linked disaccharides
inferredcites →https://doi.org/10.1021/ja0349610openalex-snapshot
2,3-Anhydrosugars in Glycoside Bond Synthesis. NMR and Computational Investigations into the Mechanism of Glycosylations with 2,3-Anhydrofuranosyl Glycosyl Sulfoxides
inferredcites →https://doi.org/10.1021/ja047578jopenalex-snapshot
The Disarming Effect of the 4,6-Acetal Group on Glycoside Reactivity: Torsional or Electronic?
inferredcites →https://doi.org/10.1021/ja068411oopenalex-snapshot
The Conformational Free Energy Landscape of β- d -Glucopyranose. Implications for Substrate Preactivation in β-Glucoside Hydrolases
inferredcites →https://doi.org/10.1021/ja307266nopenalex-snapshot
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/ja9029945openalex-snapshot
2,3-Anhydrosugars in Glycoside Bond Synthesis: Mechanism of 2-Deoxy-2-thioaryl Glycoside Formation
inferredcites →https://doi.org/10.1021/ja971239ropenalex-snapshot
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/jo0349882openalex-snapshot
Influence of the 4,6-O-Benzylidene, 4,6-O-Phenylboronate, and 4,6-O-Polystyrylboronate Protecting Groups on the Stereochemical Outcome of Thioglycoside-Based Glycosylations Mediated by 1-Benzenesulfinyl Piperidine/Triflic Anhydride and N-Iodosuccinimide/Trimethylsilyl Triflate
inferredcites →https://doi.org/10.1021/jo061417bopenalex-snapshot
On the Influence of the C2−O2 and C3−O3 Bonds in 4,6-O-Benzylidene-Directed β-Mannopyranosylation and α-Glucopyranosylation
inferredcites →https://doi.org/10.1021/jo2017026openalex-snapshot
Methodology Development and Physical Organic Chemistry: A Powerful Combination for the Advancement of Glycochemistry
inferredcites →https://doi.org/10.1021/jo202563fopenalex-snapshot
Could Diastereoselectivity in the Presence of O-2 Chiral Nonparticipating Groups Be an Indicator of Glycopyranosyl Oxacarbenium Ions in Glycosylation Reactions?
inferredcites →https://doi.org/10.1021/jo900662vopenalex-snapshot
Stereodirecting Effect of the Pyranosyl C-5 Substituent in Glycosylation Reactions
inferredcites →https://doi.org/10.1021/jo901639bopenalex-snapshot
Correlations Between Nucleophilicities and Selectivities in the Substitutions of Tetrahydropyran Acetals
inferredcites →https://doi.org/10.1021/jo902222aopenalex-snapshot
Erosion of Stereochemical Control with Increasing Nucleophilicity: O -Glycosylation at the Diffusion Limit
inferredcites →https://doi.org/10.1021/jo970944fopenalex-snapshot
Estimating the Entropic Cost of Self-Assembly of Multiparticle Hydrogen-Bonded Aggregates Based on the Cyanuric Acid·Melamine Lattice
inferredcites →https://doi.org/10.1021/ol8019956openalex-snapshot
Continuum of Mechanisms for Nucleophilic Substitutions of Cyclic Acetals
inferredcites →https://doi.org/10.1038/nchem.1404openalex-snapshot
Dissecting the mechanisms of a class of chemical glycosylation using primary 13C kinetic isotope effects
inferredcites →https://doi.org/10.1039/c2sc21610hopenalex-snapshot
On the reactivity and selectivity of donor glycosides in glycochemistry and glycobiology: trapped covalent intermediates
inferredcites →https://doi.org/10.1039/c3ob26994aopenalex-snapshot
Study of the stereoselectivity of 2-azido-2-deoxyglucosyl donors: protecting group effects
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1063/1.475428openalex-snapshot
Exchange functionals with improved long-range behavior and adiabatic connection methods without adjustable parameters: The mPW and mPW1PW models
inferredcites →https://doi.org/10.1063/1.478522openalex-snapshot
Toward reliable density functional methods without adjustable parameters: The PBE0 model
inferredcites →https://doi.org/10.1073/pnas.191362798openalex-snapshot
Solvent interactions determine carbohydrate conformation
inferredcites →https://doi.org/10.1080/00268970010018431openalex-snapshot
Left-right correlation energy
inferredcites →https://doi.org/10.1103/physreva.38.3098openalex-snapshot
Density-functional exchange-energy approximation with correct asymptotic behavior
inferredcites →https://doi.org/10.1103/physrevb.37.785openalex-snapshot
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
inferredcites →https://doi.org/10.1103/physrevb.46.6671openalex-snapshot
Atoms, molecules, solids, and surfaces: Applications of the generalized gradient approximation for exchange and correlation
inferredcites →https://doi.org/10.1103/physrevb.48.4978.2openalex-snapshot
Erratum: Atoms, molecules, solids, and surfaces: Applications of the generalized gradient approximation for exchange and correlation
inferredcites →https://doi.org/10.1103/physrevb.54.16533openalex-snapshot
Generalized gradient approximation for the exchange-correlation hole of a many-electron system
inferredcites →https://doi.org/10.1103/physrevlett.77.3865openalex-snapshot
Generalized Gradient Approximation Made Simple
inferredcites →https://doi.org/10.1103/physrevlett.78.1396openalex-snapshot
Generalized Gradient Approximation Made Simple [Phys. Rev. Lett. 77, 3865 (1996)]
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