On the public citation graph
Stereoelectronic Substituent Effects
0 signed · 170 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.199215413openalex-snapshot
Emil Fischer's Proof of the Configuration of Sugars: A Centennial Tribute
inferredcites →https://doi.org/10.1016/0160-9327(93)90217-qopenalex-snapshot
Advanced organic chemistry
inferredcites →https://doi.org/10.1016/j.tet.2004.10.039openalex-snapshot
Stereochemical substituent effects: investigation of the cyano, amide and carboxylate group
inferredcites →https://doi.org/10.1021/ja00004a066openalex-snapshot
Torsional effects in glycoside reactivity: saccharide couplings mediated by acetal protecting groups
inferredcites →https://doi.org/10.1021/ja00004a067openalex-snapshot
Reactions of phenylfluorocarbene with lithium salts. Absolute kinetics of carbenoid formation
inferredcites →https://doi.org/10.1021/ja00061a055openalex-snapshot
Protonated 3-fluoropiperidines: an unusual fluoro directing effect and a test for quantitative theories of solvation
inferredcites →https://doi.org/10.1021/ja002038hopenalex-snapshot
Synthesis and Conformational Analysis of a Sulfonium-Ion Analogue of the Glycosidase Inhibitor Castanospermine
inferredcites →https://doi.org/10.1021/ja047476topenalex-snapshot
Conformational Effects on Glycoside Reactivity: Study of the High Reactive Conformer of Glucose
inferredcites →https://doi.org/10.1021/ja992044hopenalex-snapshot
The Role of Sugar Substituents in Glycoside Hydrolysis
inferredcites →https://doi.org/10.1021/jo0205356openalex-snapshot
Equatorial Contra Axial Polar Substituents. The Relation of a Chemical Reaction to Stereochemical Substituent Constants
inferredcites →https://doi.org/10.1021/jo970677dopenalex-snapshot
Experimental and Theoretical Evidence of Through-Space Electrostatic Stabilization of the Incipient Oxocarbenium Ion by an Axially Oriented Electronegative Substituent During Glycopyranoside Acetolysis
inferredcites →https://doi.org/10.1039/b419154dopenalex-snapshot
On the electronic effects of OH groups. Synthesis and investigation of tetrahydroxylated azabicycloheptanes
inferredcites →https://doi.org/10.1039/qr9641800295openalex-snapshot
Prediction of the strengths of organic bases
inferredcites →https://doi.org/10.1063/1.1750303openalex-snapshot
The Electrostatic Influence of Substituents on the Dissociation Constants of Organic Acids. II
inferredcites →https://doi.org/10.1093/oso/9780199638079.001.0001openalex-snapshot
Molecular and Cellular Glycobiology
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9783527696239.ch6openalex-snapshot
Glycosylation with Glycosyl Sulfonates
inferred← citeshttps://doi.org/10.1002/adsc.200900662openalex-snapshot
Iron Chloride/4‐Acetamido‐TEMPO/Sodium Nitrite‐Catalyzed Aerobic Oxidation of Primary Alcohols to the Aldehydes
inferred← citeshttps://doi.org/10.1002/ange.200802036openalex-snapshot
Neue Prinzipien für die Bildung von glycosidischen Bindungen
inferred← citeshttps://doi.org/10.1002/ange.201409797openalex-snapshot
The Isothiocyanato Moiety: An Ideal Protecting Group for the Stereoselective Synthesis of Sialic Acid Glycosides and Subsequent Diversification
inferred← citeshttps://doi.org/10.1002/anie.200802036openalex-snapshot
New Principles for Glycoside‐Bond Formation
inferred← citeshttps://doi.org/10.1002/anie.201409797openalex-snapshot
The Isothiocyanato Moiety: An Ideal Protecting Group for the Stereoselective Synthesis of Sialic Acid Glycosides and Subsequent Diversification
inferred← citeshttps://doi.org/10.1002/cbic.201700080openalex-snapshot
Conformational Behaviour of Azasugars Based on Mannuronic Acid
inferred← citeshttps://doi.org/10.1002/chem.200601111openalex-snapshot
Glycosidation–Anomerisation Reactions of 6,1‐Anhydroglucopyranuronic Acid and Anomerisation of β‐ D ‐Glucopyranosiduronic Acids Promoted by SnCl4
inferred← citeshttps://doi.org/10.1002/chem.200700947openalex-snapshot
Going to Extremes: “Super” Armed Glycosyl Donors in Glycosylation Chemistry
inferred← citeshttps://doi.org/10.1002/chem.200701818openalex-snapshot
TEMPO/HCl/NaNO 2 Catalyst: A Transition‐Metal‐Free Approach to Efficient Aerobic Oxidation of Alcohols to Aldehydes and Ketones Under Mild Conditions
inferred← citeshttps://doi.org/10.1002/chem.200800960openalex-snapshot
Stereoselective Synthesis of L ‐Guluronic Acid Alginates
inferred← citeshttps://doi.org/10.1002/chem.201002313openalex-snapshot
Quantifying Electronic Effects of Common Carbohydrate Protecting Groups in a Piperidine Model System
inferred← citeshttps://doi.org/10.1002/chem.201003251openalex-snapshot
Direct Experimental Evidence for the High Chemical Reactivity of α‐ and β‐Xylopyranosides Adopting a 2,5B Conformation in Glycosyl Transfer
inferred← citeshttps://doi.org/10.1002/chem.201100020openalex-snapshot
Quantifying the Electronic Effects of Carbohydrate Hydroxy Groups by Using Aminosugar Models
inferred← citeshttps://doi.org/10.1002/chem.201505019openalex-snapshot
Determination of the Influence of Side‐Chain Conformation on Glycosylation Selectivity using Conformationally Restricted Donors
inferred← citeshttps://doi.org/10.1002/chem.201900651openalex-snapshot
Furanosyl Oxocarbenium Ion Conformational Energy Landscape Maps as a Tool to Study the Glycosylation Stereoselectivity of 2‐Azidofuranoses, 2‐Fluorofuranoses and Methyl Furanosyl Uronates
inferred← citeshttps://doi.org/10.1002/chem.202003480openalex-snapshot
Exploratory N‐Protecting Group Manipulation for the Total Synthesis of Zwitterionic Shigella sonnei Oligosaccharides
inferred← citeshttps://doi.org/10.1002/chin.200629263openalex-snapshot
Stereoelectronic Substituent Effects
inferred← citeshttps://doi.org/10.1002/cmdc.201200582openalex-snapshot
Benzenesulfonamides: A Unique Class of Chemokine Receptor Type 4 Inhibitors
inferred← citeshttps://doi.org/10.1002/cphc.202400972openalex-snapshot
Proton Changes the Rules of the Game: Insight into the Nature of “Proton Sponges”
inferred← citeshttps://doi.org/10.1002/ejoc.200800696openalex-snapshot
Acetolysis of 6‐Deoxysugar Disaccharide Building Blocks: exo versus endo Activation
inferred← citeshttps://doi.org/10.1002/ejoc.201101385openalex-snapshot
pKa‐Determination and Conformational Studies by NMR Spectroscopy of D ‐Altrose‐Containing and other Pseudodisaccharides as Glycosidase Inhibitor Candidates
inferred← citeshttps://doi.org/10.1002/ejoc.201101708openalex-snapshot
Hydroxy Group Acidities of Partially Protected Glycopyranosides
inferred← citeshttps://doi.org/10.1002/ejoc.201501037openalex-snapshot
Total Syntheses of Laevigatins A and E
inferred← citeshttps://doi.org/10.1002/ejoc.201601355openalex-snapshot
l ‐Rhamnosylation: The Solvent is the Solution
inferred← citeshttps://doi.org/10.1002/ejoc.202001130openalex-snapshot
Conformational Lock of Glycosyl Donors Using Cyclic Carbamates
inferred← citeshttps://doi.org/10.1002/macp.201700119openalex-snapshot
Influence of Stereochemistry on Relative Reactivities of Glucosyl and Mannosyl Residues in Konjac Glucomannan (KGM)
inferred← citeshttps://doi.org/10.1002/slct.202200963openalex-snapshot
Stereoselective Synthesis of α ‐ʟ‐Rhamnopyranosides from ʟ‐Rhamnal Employing Ruthenium‐Catalysis
inferred← citeshttps://doi.org/10.1007/128_2010_106openalex-snapshot
Superarmed and Superdisarmed Building Blocks in Expeditious Oligosaccharide Synthesis
inferred← citeshttps://doi.org/10.1007/978-1-4614-8268-0_4openalex-snapshot
Conformations and Chemistry of Oxocarbenium Ion
inferred← citeshttps://doi.org/10.1007/978-1-4614-8268-0_5openalex-snapshot
Armed-Disarmed Concept in the Synthesis of Glycosidic Bond
inferred← citeshttps://doi.org/10.1007/978-3-540-30429-6_1openalex-snapshot
Structure and Conformation of Carbohydrates
inferred← citeshttps://doi.org/10.1007/s10570-016-1131-7openalex-snapshot
Substituent effects on the kinetics of acid-catalyzed hydrolysis of methyl cellulose
inferred← citeshttps://doi.org/10.1007/s10570-025-06424-yopenalex-snapshot
On the structure, conformation and reactivity of β-1,4-linked plant cell wall glycans: why are xylan polysaccharides or furanosyl substituents easier to hydrolyze than cellulose?
inferred← citeshttps://doi.org/10.1007/s40203-025-00544-wopenalex-snapshot
Targeting Alzheimer’s diseases via nitro-substituted Schiff base derivatives: synthesis, DFT, and molecular dynamics studies
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00602-9openalex-snapshot
6.01 Synthesis of Glycosides
inferred← citeshttps://doi.org/10.1016/b978-0-12-385464-3.00001-7openalex-snapshot
The Literature of Heterocyclic Chemistry, Part X, 2005–2007
inferred← citeshttps://doi.org/10.1016/b978-0-12-819475-1.00073-0openalex-snapshot
Stereoelectronic Effects in Glycosylation Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-819475-1.00074-2openalex-snapshot
The Oxocarbenium Ion Intermediate
inferred← citeshttps://doi.org/10.1016/b978-044451967-2/00011-8openalex-snapshot
Strategies in Oligosaccharide Synthesis
inferred← citeshttps://doi.org/10.1016/j.apenergy.2017.09.023openalex-snapshot
Characterisation and kinetic study of carbon dioxide absorption by an aqueous diamine solution
inferred← citeshttps://doi.org/10.1016/j.biortech.2018.11.039openalex-snapshot
Quantitation of fast hydrolysis of cellulose catalyzed by its substituents for potential biomass conversion
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.09.034openalex-snapshot
γ-Hydroxyethyl piperidine iminosugar and N-alkylated derivatives: A study of their activity as glycosidase inhibitors and as immunosuppressive agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2017.07.026openalex-snapshot
α-Geminal disubstituted pyrrolidine iminosugars and their C-4-fluoro analogues: Synthesis, glycosidase inhibition and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.carres.2009.08.037openalex-snapshot
The role of sugar configuration in the acetolysis of 6-deoxyhexose methyl glycosides
inferred← citeshttps://doi.org/10.1016/j.carres.2010.02.027openalex-snapshot
The impact of oxacarbenium ion conformers on the stereochemical outcome of glycosylations
inferred← citeshttps://doi.org/10.1016/j.carres.2012.01.026openalex-snapshot
Synthesis of a tetrasaccharide analog corresponding to the repeating unit of the O-polysaccharide of Salmonella enterica O59: unexpected stereo outcome in glycosylation
inferred← citeshttps://doi.org/10.1016/j.carres.2014.06.020openalex-snapshot
A propos of glycosyl cations and the mechanism of chemical glycosylation; the current state of the art
inferred← citeshttps://doi.org/10.1016/j.carres.2015.02.007openalex-snapshot
Common side reactions of the glycosyl donor in chemical glycosylation
inferred← citeshttps://doi.org/10.1016/j.carres.2015.03.004openalex-snapshot
Synthesis, conformational study, glycosidase inhibitory activity and molecular docking studies of dihydroxylated 4- and 5-amino-iminosugars
inferred← citeshttps://doi.org/10.1016/j.carres.2025.109527openalex-snapshot
Bi(OTf)3-promoted direct activation of formidable per-O-acetylated ʟ-rhamnose Donor: Stereoselective access to α-ʟ-rhamnopyranosides
inferred← citeshttps://doi.org/10.1016/j.ccr.2023.215392openalex-snapshot
Advances in membrane-based chiral separation
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.217350openalex-snapshot
Stereoelectronic effects: From molecules to single-molecule devices
inferred← citeshttps://doi.org/10.1016/j.crci.2010.03.030openalex-snapshot
Glycosyl donors in “unusual” conformations – influence on reactivity and selectivity
inferred← citeshttps://doi.org/10.1016/j.crci.2010.05.010openalex-snapshot
Novel protecting groups in carbohydrate chemistry
inferred← citeshttps://doi.org/10.1016/j.crci.2010.05.016openalex-snapshot
Concise synthesis of 1,3-di-O-substituted tetrahydropyran derivatives as conformationally stable pyranose mimetics
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.03.004openalex-snapshot
Unraveling chemical glycosylation: DFT insights into factors imparting stereoselectivity
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2011.05.031openalex-snapshot
Synthesis of monofluorinated isofagomine analogues and evaluation as glycosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144188openalex-snapshot
Exploring density functional theory to gain insight into the enolimine-ketoenamine tautomerism of dihydroxyl Schiff bases derived from 4-(diethylamino)salicylaldehyde and investigating their use as antidiabetes and antioxidant agents
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144582openalex-snapshot
Influence of mono- and di-bromo substitution on the structure conformation and supramolecular assembly of schiff base derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2009.01.019openalex-snapshot
A 2,4-O-[(Z)-2-butenylene]-bridged glucopyranose: efficient construction of the bicyclic skeleton and its axial-rich twist-boat conformation
inferred← citeshttps://doi.org/10.1016/j.tet.2009.02.067openalex-snapshot
Stereoselectivity of glycosylations of conformationally restricted mannuronate esters
inferred← citeshttps://doi.org/10.1016/j.tet.2009.02.079openalex-snapshot
Synthesis and biological evaluation of potent glycosidase inhibitors: 4-deoxy-4,4-difluoroisofagomine and analogues
inferred← citeshttps://doi.org/10.1016/j.tet.2012.06.068openalex-snapshot
Influence of bromide ions on the synthesis of anomeric thiocyanates
inferred← citeshttps://doi.org/10.1016/j.tet.2016.07.081openalex-snapshot
A mild method for regioselective de-O-methylation of saccharides by Co2(CO)8/Et3SiH/CO system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.024openalex-snapshot
A potential glucuronate glycosyl donor with 2-O-acyl-6,3-lactone structure: efficient synthesis of glycosaminoglycan disaccharides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.11.052openalex-snapshot
Super arming of a glycosyl donor using a molecular lever
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.07.078openalex-snapshot
Hydroxylated oxanes as xyloside analogs for determination of the minimal binding requirements of β4GalT7
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00243openalex-snapshot
Mechanisms of Stereodirecting Participation and Ester Migration from Near and Far in Glycosylation and Related Reactions
inferred← citeshttps://doi.org/10.1021/acs.chemrev.2c00029openalex-snapshot
Synthesis and Glycosidation of Anomeric Halides: Evolution from Early Studies to Modern Methods of the 21st Century
inferred← citeshttps://doi.org/10.1021/acs.chemrev.2c00086openalex-snapshot
The Synthesis and Glycoside Formation of Polyfluorinated Carbohydrates
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5c00638openalex-snapshot
Chemical Glycosylations in Water and Aqueous Media
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00051openalex-snapshot
Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00083openalex-snapshot
The Experimental Evidence in Support of Glycosylation Mechanisms at the SN1–SN2 Interface
inferred← citeshttps://doi.org/10.1021/acs.joc.0c03015openalex-snapshot
Development of α-Selective Glycosylation for the Synthesis of Deoxyfluorinated TN Antigen Analogues
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02207openalex-snapshot
Rationalizing the Stereoelectronic Influence of Interglycosidic Bond Conformations on the Reactivity of 1,4-O-Linked Disaccharide Donors
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01496openalex-snapshot
Stereodirecting Effect of Esters at the 4-Position of Galacto- and Glucopyranosyl Donors: Effect of 4-C-Methylation on Side-Chain Conformation and Donor Reactivity, and Influence of Concentration and Stoichiometry on Distal Group Participation
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02956openalex-snapshot
The Stereochemical Outcome of Galactosylations Is Influenced by Both the Position and Electron-Withdrawing Power of Distal Acyl Protecting Groups
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02203openalex-snapshot
Absence of Stereodirecting Participation by 2‑ O ‑Alkoxycarbonylmethyl Ethers in 4,6‑ O ‑Benzylidene-Directed Mannosylation
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00814openalex-snapshot
Substituent Effects on NMR Chemical Shifts and Cyclic Hydrogen Bonding in 2-Pyridone Dimers: An Accurate Approach to Hammett Constant Determination Linking Structure, Energetics, and Electron Distribution
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00528openalex-snapshot
Remote Electronic Effects by Ether Protecting Groups Fine-Tune Glycosyl Donor Reactivity
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01685openalex-snapshot
The Origin of High Stereoselectivity in Di-tert-butylsilylene-Directed α-Galactosylation
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02221openalex-snapshot
Stereoselective Synthesis of 5-epi-α-Sialosides Related to the Pseudaminic Acid Glycosides. Reassessment of the Stereoselectivity of the 5-Azido-5-deacetamidosialyl Thioglycosides and Use of Triflate as Nucleophile in the Zbiral Deamination of Sialic Acids
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02809openalex-snapshot
Synthesis of Double-Modified Xyloside Analogues for Probing the β4GalT7 Active Site
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02891openalex-snapshot
Synthesis of Conformationally-Locked cis- and trans-Bicyclo[4.4.0] Mono-, Di-, and Trioxadecane Modifications of Galacto- and Glucopyranose; Experimental Limiting 3JH,H Coupling Constants for the Estimation of Carbohydrate Side Chain Populations and Beyond
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01459openalex-snapshot
Interplay of Protecting Groups and Side Chain Conformation in Glycopyranosides. Modulation of the Influence of Remote Substituents on Glycosylation?
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00830openalex-snapshot
Conformationally Switchable Glycosyl Donors
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00078openalex-snapshot
Synthesis of Glycosyl Chlorides and Bromides by Chelation Assisted Activation of Picolinic Esters under Mild Neutral Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01430openalex-snapshot
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
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02724openalex-snapshot
Influence of C-4 Axial/Equatorial Configuration and Neighboring Group/Remote Group Participation (NGP/RGP) Driven Conformational Evidence in Chemoselective Activation of Glycals
inferred← citeshttps://doi.org/10.1021/acscatal.1c00896openalex-snapshot
Side Chain Conformation Restriction in the Catalysis of Glycosidic Bond Formation by Leloir Glycosyltransferases, Glycoside Phosphorylases, and Transglycosidases
inferred← citeshttps://doi.org/10.1021/acscatal.1c02750openalex-snapshot
GH47 and Other Glycoside Hydrolases Catalyze Glycosidic Bond Cleavage with the Assistance of Substrate Super-Arming at the Transition State
inferred← citeshttps://doi.org/10.1021/acscatal.8b02440openalex-snapshot
Biomimetic Glycoside Hydrolysis by a Microgel Templated with a Competitive Glycosidase Inhibitor
inferred← citeshttps://doi.org/10.1021/acscentsci.9b00042openalex-snapshot
Defining the SN1 Side of Glycosylation Reactions: Stereoselectivity of Glycopyranosyl Cations
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/ja071955lopenalex-snapshot
“Super Armed” Glycosyl Donors: Conformational Arming of Thioglycosides by Silylation
inferred← citeshttps://doi.org/10.1021/ja110332ropenalex-snapshot
Borinic Acid-Catalyzed Regioselective Acylation of Carbohydrate Derivatives
inferred← citeshttps://doi.org/10.1021/ja301480gopenalex-snapshot
Completely β-Selective Glycosylation Using 3,6-O-(o-Xylylene)-Bridged Axial-Rich Glucosyl Fluoride
inferred← citeshttps://doi.org/10.1021/ja307355nopenalex-snapshot
Effect of Remote Picolinyl and Picoloyl Substituents on the Stereoselectivity of Chemical Glycosylation
inferred← citeshttps://doi.org/10.1021/ja405588xopenalex-snapshot
Probing the Influence of a 4,6-O-Acetal on the Reactivity of Galactopyranosyl Donors: Verification of the Disarming Influence of thetrans–gaucheConformation of C5–C6 Bonds
inferred← citeshttps://doi.org/10.1021/ja410683yopenalex-snapshot
Influence of Side Chain Conformation and Configuration on Glycosyl Donor Reactivity and Selectivity as Illustrated by Sialic Acid Donors Epimeric at the 7-Position
inferred← citeshttps://doi.org/10.1021/ja8052706openalex-snapshot
Remarkable Oxidation Stability of Glycals: Excellent Substrates for Cerium(IV)-Mediated Radical Reactions
inferred← citeshttps://doi.org/10.1021/jacs.0c05525openalex-snapshot
Dissecting the Essential Role of Anomeric β-Triflates in Glycosylation Reactions
inferred← citeshttps://doi.org/10.1021/jacs.5b06126openalex-snapshot
Cation Clock Reactions for the Determination of Relative Reaction Kinetics in Glycosylation Reactions: Applications to Gluco- and Mannopyranosyl Sulfoxide and Trichloroacetimidate Type Donors
inferred← citeshttps://doi.org/10.1021/jacs.5c03519openalex-snapshot
Elucidating the Curtin–Hammett Principle in Glycosylation Reactions: The Decisive Role of Equatorial Glycosyl Triflates
inferred← citeshttps://doi.org/10.1021/jacs.8b09654openalex-snapshot
Synthesis and Stereocontrolled Equatorially Selective Glycosylation Reactions of a Pseudaminic Acid Donor: Importance of the Side-Chain Conformation and Regioselective Reduction of Azide Protecting Groups
inferred← citeshttps://doi.org/10.1021/jm701239aopenalex-snapshot
Potent Non-Nucleoside Inhibitors of the Measles Virus RNA-Dependent RNA Polymerase Complex
inferred← citeshttps://doi.org/10.1021/jo062411popenalex-snapshot
Facile Oxidative Cleavage of 4-O-Benzyl Ethers with Dichlorodicyanoquinone in Rhamno- and Mannopyranosides
inferred← citeshttps://doi.org/10.1021/jo100366vopenalex-snapshot
One-Pot Syntheses of Immunostimulatory Glycolipids
inferred← citeshttps://doi.org/10.1021/jo101090fopenalex-snapshot
SnCl 4 - and TiCl 4 -Catalyzed Anomerization of Acylated O - and S -Glycosides: Analysis of Factors That Lead to Higher α:β Anomer Ratios and Reaction Rates
inferred← citeshttps://doi.org/10.1021/jo2019174openalex-snapshot
Glycosidation of Thioglycosides in the Presence of Bromine: Mechanism, Reactivity, and Stereoselectivity
inferred← citeshttps://doi.org/10.1021/jo3011655openalex-snapshot
Stereoselective C-Glycoside Formation with 2-O-Benzyl-4,6-O-benzylidene Protected 3-Deoxy Gluco- and Mannopyranoside Donors: Comparison with O-Glycoside Formation
inferred← citeshttps://doi.org/10.1021/jo3020243openalex-snapshot
Hyperconjugation Involving Strained Carbon–Carbon Bonds. Structural Analysis of Ester and Ether Derivatives and One-Bond13C–13C Coupling Constants of α- and β-Nopinol
inferred← citeshttps://doi.org/10.1021/jo4012464openalex-snapshot
Conformationally Armed 3,6-Tethered Glycosyl Donors: Synthesis, Conformation, Reactivity, and Selectivity
inferred← citeshttps://doi.org/10.1021/jo801028yopenalex-snapshot
The Naturally Occurring Ketene Acetal Benesudon: Total Synthesis and Assignment of Relative and Absolute Stereochemistry
inferred← citeshttps://doi.org/10.1021/jo801630mopenalex-snapshot
Does Neighboring Group Participation by Non-Vicinal Esters Play a Role in Glycosylation Reactions? Effective Probes for the Detection of Bridging Intermediates
inferred← citeshttps://doi.org/10.1021/jo8017846openalex-snapshot
The Effect of Electrostatic Interactions on Conformational Equilibria of Multiply Substituted Tetrahydropyran Oxocarbenium Ions
inferred← citeshttps://doi.org/10.1021/jo901639bopenalex-snapshot
Correlations Between Nucleophilicities and Selectivities in the Substitutions of Tetrahydropyran Acetals
inferred← citeshttps://doi.org/10.1021/ol070427bopenalex-snapshot
Highly β-Selective O-Glucosidation Due to the Restricted Twist-Boat Conformation
inferred← citeshttps://doi.org/10.1021/ol2016862openalex-snapshot
Mannopyranosyl Uronic Acid Donor Reactivity
inferred← citeshttps://doi.org/10.1021/ol402371bopenalex-snapshot
Superarming of Glycosyl Donors by Combined Neighboring and Conformational Effects
inferred← citeshttps://doi.org/10.1021/ol403722fopenalex-snapshot
β-Selective Mannosylation with a 4,6-Silylene-Tethered Thiomannosyl Donor
inferred← citeshttps://doi.org/10.1021/ol702509aopenalex-snapshot
Oxidative Decarboxylation as a Route to Ketene Acetals: Assignment of Relative and Absolute Stereochemistry to the Fungal Metabolite Benesudon by Total Synthesis
inferred← citeshttps://doi.org/10.1038/nchem.399openalex-snapshot
Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research
inferred← citeshttps://doi.org/10.1038/s41429-019-0165-0openalex-snapshot
Step-economy synthesis of β-steryl sialosides using a sialyl iodide donor
inferred← citeshttps://doi.org/10.1039/b801305eopenalex-snapshot
Conformationally armed glycosyl donors: reactivity quantification, new donors and one pot reactions
inferred← citeshttps://doi.org/10.1039/b807064dopenalex-snapshot
Direct formation of β-glycosides of N-acetyl glycosamines mediated by rare earth metal triflates
inferred← citeshttps://doi.org/10.1039/b916088dopenalex-snapshot
Mechanism of chemical O-glycosylation: from early studies to recent discoveries
inferred← citeshttps://doi.org/10.1039/bk9781849733274-00001openalex-snapshot
Structures of Open-chain Forms of Reducing Sugars and Related Molecules. Mechanistic Probes of Sugar Carbonyl Group Additions
inferred← citeshttps://doi.org/10.1039/bk9781849733274-00072openalex-snapshot
Nucleophilic Substitution at the Anomeric Centre
inferred← citeshttps://doi.org/10.1039/bk9781849733274-00415openalex-snapshot
Heterolytic Reactions of OH Groups
inferred← citeshttps://doi.org/10.1039/c2cc17623hopenalex-snapshot
β-Rhamnosides from 6-thio mannosides
inferred← citeshttps://doi.org/10.1039/c3cs35457aopenalex-snapshot
Design of chemical glycosyl donors: does changing ring conformation influence selectivity/reactivity?
inferred← citeshttps://doi.org/10.1039/c4md00072bopenalex-snapshot
Synthesis of 4′-deoxy-4′-fluoro neamine and 4′-deoxy-4′-fluoro 4′- epi neamine
inferred← citeshttps://doi.org/10.1039/c6cc10076gopenalex-snapshot
Catalytic stereospecific O -glycosylation
inferred← citeshttps://doi.org/10.1039/c6ob02427kopenalex-snapshot
On the nature of the electronic effect of multiple hydroxyl groups in the 6-membered ring – the effects are additive but steric hindrance plays a role too
inferred← citeshttps://doi.org/10.1039/c7ob02966gopenalex-snapshot
On the generality of the superarmament of glycosyl donors
inferred← citeshttps://doi.org/10.1039/c8sc02788aopenalex-snapshot
Stereoselective organocatalyzed glycosylations – thiouracil, thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadings
inferred← citeshttps://doi.org/10.1039/d4qo02329copenalex-snapshot
Investigating the stereo-directing effect of remote participating groups on selectivity in the 2-deoxyglycosylation of galactal
inferred← citeshttps://doi.org/10.1042/bj20141412openalex-snapshot
Glycosynthesis in a waterworld: new insight into the molecular basis of transglycosylation in retaining glycoside hydrolases
inferred← citeshttps://doi.org/10.1055/s-0040-1719854openalex-snapshot
Silylated Sugars – Synthesis and Properties
inferred← citeshttps://doi.org/10.1080/07328303.2012.749264openalex-snapshot
Mechanism of Chemical Glycosylation: Focus on the Mode of Activation and Departure of Anomeric Leaving Groups
inferred← citeshttps://doi.org/10.1080/07328303.2018.1462372openalex-snapshot
Immobilization of glycans on solid surfaces for application in glycomics
inferred← citeshttps://doi.org/10.1515/pac-2019-0306openalex-snapshot
One-pot oligosaccharide synthesis: latent-active method of glycosylations and radical halogenation activation of allyl glycosides
inferred← citeshttps://doi.org/10.2139/ssrn.5388406openalex-snapshot
Influence of Mono- and Di-Bromo Substitution on the Structure Conformation and Supramolecular Assembly of Schiff Base Derivatives
inferred← citeshttps://doi.org/10.3390/biom16050680openalex-snapshot
Targeting Selectivity: Improving Golgi α-Mannosidase II (GMII) Inhibitors Through In Silico Studies
inferred← citeshttps://doi.org/10.3390/ijms221910357openalex-snapshot
How Substitution Combines with Non-Covalent Interactions to Modulate 1,4-Naphthoquinone and Its Derivatives Molecular Features—Multifactor Studies
inferred← citeshttps://doi.org/10.3390/molecules30081675openalex-snapshot
Antifungal and Antioxidant Activity of Thiourea Derivatives Against Nosocomial Candida auris Strains Isolated in Romania
inferred← citeshttps://doi.org/10.3762/bjoc.12.227openalex-snapshot
Useful access to enantiomerically pure protected inositols from carbohydrates: the aldohexos-5-uloses route
inferred← citeshttps://doi.org/10.3762/bjoc.13.12openalex-snapshot
Silyl-protective groups influencing the reactivity and selectivity in glycosylations
inferred← citeshttps://doi.org/10.70675/5d559c45z8e35z48d4z8d10zd21d2d56a2b6openalex-snapshot
Préparation et applications de nouveaux xylosides comportant des aglycones fonctionnalisés pour la synthèse organique et la catalyse homogène
inferred← citeshttps://doi.org/10.70675/90e72228z707fz4f01z88d6z19cef2e17425openalex-snapshot
Exploiter des superacides pour générer et caractériser des espèces ioniques clés dans le domaine des glycosciences
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.