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Solid-Phase Synthesis of β-Mannosides
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527618255openalex-snapshot
Carbohydrates in Chemistry and Biology
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Isomeric Lactam Catenanes and the Mechanism of their Formation
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Monitoring the Progress of Solid‐Phase Oligosaccharide Synthesis by High‐Resolution Magic Angle Spinning NMR: Observations of Enhanced Selectivity for β‐Glycoside Formation from α‐1,2‐Anhydrosugar Donors in Solid‐Phase Couplings
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Synthesis of 4- O - d -Mannopyranosyl-α- d -glucopyranosides by Intramolecular Glycosylation of 6- O -Tethered Mannosyl Donors
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An unusual example of steric buttressing in glycosylation
inferredcites →https://doi.org/10.1016/s0040-4039(00)01497-0openalex-snapshot
Can preferential β-mannopyranoside formation with 4,6-O-benzylidene protected mannopyranosyl sulfoxides be reached with trichloroacetimidates?
inferredcites →https://doi.org/10.1016/s0300-9084(97)83520-1openalex-snapshot
Modern methods in carbohydrate synthesis
inferredcites →https://doi.org/10.1021/ar9600648openalex-snapshot
Solid-Phase Synthesis of Oligosaccharides and Glycoconjugates by the Glycal Assembly Method: A Five Year Retrospective
inferredcites →https://doi.org/10.1021/cr9903104openalex-snapshot
Solid-Phase Oligosaccharide Synthesis and Combinatorial Carbohydrate Libraries
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/ja00199a081openalex-snapshot
Glycosylation of unreactive substrates
inferredcites →https://doi.org/10.1021/ja964021yopenalex-snapshot
A Fundamentally New, Simple, Stereospecific Synthesis of Oligosaccharides Containing the β-Mannopyranosyl and β-Rhamnopyranosyl Linkage
inferredcites →https://doi.org/10.1021/jo9601223openalex-snapshot
A Solvation-Assisted Model for Estimating Anomeric Reactivity. Predicted versus Observed Trends in Hydrolysis of n-Pentenyl Glycosides1
inferredcites →https://doi.org/10.1126/science.1057324openalex-snapshot
Automated Solid-Phase Synthesis of Oligosaccharides
inferredcites →https://doi.org/10.1126/science.1057594openalex-snapshot
Redox State of Mars' Upper Mantle and Crust from Eu Anomalies in Shergottite Pyroxenes
inferredcites →https://doi.org/10.1126/science.274.5292.1520openalex-snapshot
Parallel Synthesis and Screening of a Solid Phase Carbohydrate Library
inferredcites →https://doi.org/10.1139/v94-181openalex-snapshot
The synthesis of β-mannopyranosides by intramolecular aglycon delivery: scope and limitations of the existing methodology
inferredcites →https://doi.org/10.4052/tigg.5.121openalex-snapshot
2-Oxo- and 2-Oximinoglycosyl Halides: Versatile Glycosyl Donors for the Construction of .BETA.-D-Mannose and .BETA.-D-Mannosamine-containing Oligosaccharides.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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1-Benzenesulfinyl Piperidine
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Trifluoromethanesulfonic Anhydride
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Trifluoromethanesulfonic Anhydride
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Trifluoromethanesulfonic Anhydride
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Glycosylation with Sulfoxides and Sulfinates as Donors or Promoters
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Synthetic Approaches to Bioactive Carbohydrates
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Glycoside Synthesis from 1‐Sulfur/Selenium‐Substituted Derivatives: Sections 4.1 and 4.2
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Glycosylation with Glycosyl Sulfonates
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Preactivation: An Alternative Strategy in Stereoselective Glycosylation and Oligosaccharide Synthesis
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Neue Prinzipien für die Bildung von glycosidischen Bindungen
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Automated Solid‐Phase Synthesis of β‐Mannuronic Acid Alginates
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New Principles for Glycoside‐Bond Formation
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Automated Solid‐Phase Synthesis of β‐Mannuronic Acid Alginates
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Synthesis of Bradyrhizose Oligosaccharides Relevant to the Bradyrhizobium O‐Antigen
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Chemical Synthesis Elucidates the Key Antigenic Epitope of the Autism‐Related Bacterium Clostridium bolteae Capsular Octadecasaccharide
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Rate‐Dependent Inverse‐Addition β‐Selective Mannosylation and Contiguous Sequential Glycosylation Involving β‐Mannosidic Bond Formation
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Automated Solid‐Phase Synthesis of Protected Oligosaccharides Containing β‐Mannosidic Linkages
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Strong Aphicidal Activity of GlcNAc(β1→4)Glc Disaccharides: Synthesis, Physiological Effects, and Chitinase Inhibition
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Highly Stereoselective β‐Mannopyranosylation via the 1‐α‐Glycosyloxy‐isochromenylium‐4‐gold(I) Intermediates
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Photoswitchable Carbohydrate‐Based Macrocyclic Azobenzene: Synthesis, Chiroptical Switching, and Multistimuli‐Responsive Self‐Assembly
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Donor Preactivation‐Based Glycosylation: An Efficient Strategy for Glycan Synthesis
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Remote Participation‐Assisted Synthesis of β‐Mannosides
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Glycosylations Directed by the Armed‐Disarmed Effect with Acceptors Containing a Single Ester Group
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Self‐Immolative Reduction of Trifluoromethyl Sulfoxides Promoted by Trifluoromethanesulfonic Anhydride
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Advances in Organoboron‐Catalyzed Regio‐ and Stereoselective Glycosylation
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Chemical O‐Glycosylations: An Overview
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Borylated Polyolefins and their Applications
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One-pot strategy: A highly economical tool in organic synthesis and medicinal chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-12-819475-1.00016-xopenalex-snapshot
1,2-cis O-Glycosylation Methods
inferred← citeshttps://doi.org/10.1016/b978-0-240-52118-3.00005-3openalex-snapshot
Oligosaccharide Synthesis
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Recent advances of the stereoselective bimodal glycosylations for the synthesis of various glucans
inferred← citeshttps://doi.org/10.1016/bs.accb.2022.10.005openalex-snapshot
Conformationally restricted donors for stereoselective glycosylation
inferred← citeshttps://doi.org/10.1016/j.carres.2013.09.001openalex-snapshot
Applications of organoboron compounds in carbohydrate chemistry and glycobiology: analysis, separation, protection, and activation
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Novel 1,2- cis -stereoselective glycosylations utilizing organoboron reagents and their application to natural products and complex oligosaccharide synthesis
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Lewis acidic organoboron polymers
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.03.004openalex-snapshot
Unraveling chemical glycosylation: DFT insights into factors imparting stereoselectivity
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Direct and stereoselective synthesis of β-d-mannosides using 4,6-O-benzylidene-protected mannosyl diethyl phosphite as a donor
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Synthesis of the pentasaccharide repeating unit of the O-antigenic polysaccharide of enteroaggregative Escherichia coli O44:H18 strain
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Synthesis of the pentasaccharide repeating unit corresponding to the cell wall O-antigen of Shigella boydii type 16
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Synthesis of the β-d-mannose containing tetrasaccharide repeating unit corresponding to the O-specific polysaccharide of Salmonella cerro O:18
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Disarming, non-participating 2-O-protecting groups in manno- and rhamnopyranosylation: scope and limitations of sulfonates, vinylogous esters, phosphates, cyanates, and nitrates
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Synthesis of a tetrasaccharide repeating unit of O-antigenic polysaccharide of Salmonella enteritidis by use of unique and odorless dodecyl thioglycosyl donors
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Straightforward stereoselective synthesis of 1-thio-β-d-mannosides and 1-thio-β-l-rhamnosides
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Chapter 5 Oligosaccharide Synthesis: From Conventional Methods to Modern Expeditious Strategies
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“One-Pot” Protection, Glycosylation, and Protection–Glycosylation Strategies of Carbohydrates
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Site-Selective Functionalization of Hydroxyl Groups in Carbohydrate Derivatives
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Chemical Synthesis of Residue-Selectively 13C and 2H Double-Isotope-Labeled Oligosaccharides as Chemical Probes for the NMR-Based Conformational Analysis of Oligosaccharides
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Conformationally Constrained Glycosyl Donors as Tools to Control Glycosylation Outcomes
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Boronic Acid-Catalyzed Regioselective Koenigs–Knorr-Type Glycosylation
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Zinc(II) Iodide-Directed β-Mannosylation: Reaction Selectivity, Mode, and Application
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Sequential Functionalizations of Carbohydrates Enabled by Boronic Esters as Switchable Protective/Activating Groups
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Stereoselective Phenylselenoglycosylation of Glycals Bearing a Fused Carbonate Moiety toward the Synthesis of 2-Deoxy-β-galactosides and β-Mannosides
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Stereodivergent Mannosylation Using 2-O-(ortho-Tosylamido)benzyl Group
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Boronic Acid Catalysis for Diol Activation under Lewis Base Promotion: Site-Selective Propargylation of Carbohydrates
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Mechanism of a Chemical Glycosylation Reaction
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Advances in Synthetic Approaches towards Glycoantigens
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2-Oxoglycosyl (“Ulosyl”) and 2-Oximinoglycosyl Bromides: Versatile Donors for the Expedient Assembly of Oligosaccharides with β- d -Mannose, β- l -Rhamnose, N -Acetyl-β- d -mannosamine, and N -Acetyl-β- d -mannosaminuronic Acid Units
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Electrochemical Generation of Glycosyl Triflate Pools
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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
inferred← citeshttps://doi.org/10.1021/jo0526789openalex-snapshot
Enhanced Diastereoselectivity in β-Mannopyranosylation through the Use of Sterically Minimal Propargyl Ether Protecting Groups
inferred← citeshttps://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
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On the Use of 3,5- O -Benzylidene and 3,5- O -(Di- tert -butylsilylene)-2- O -benzylarabinothiofuranosides and Their Sulfoxides as Glycosyl Donors for the Synthesis of β-Arabinofuranosides: Importance of the Activation Method
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Methodology Development and Physical Organic Chemistry: A Powerful Combination for the Advancement of Glycochemistry
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Influence of O6 in Mannosylations Using Benzylidene Protected Donors: Stereoelectronic or Conformational Effects?
inferred← citeshttps://doi.org/10.1021/jo8022439openalex-snapshot
Stereocontrolled Synthesis of d - and l -β-Rhamnopyranosides with 4- O -6- S -α-Cyanobenzylidene-Protected 6-Thiorhamnopyranosyl Thioglycosides
inferred← citeshttps://doi.org/10.1021/ol0340890openalex-snapshot
Direct Synthesis of the β- l -Rhamnopyranosides
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Oxazolidinone Protection of N-Acetylglucosamine Confers High Reactivity on the 4-Hydroxy Group in Glycosylation
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The 4,6-O-[α-(2-(2- Iodophenyl)ethylthiocarbonyl)benzylidene] Protecting Group: Stereoselective Glycosylation, Reductive Radical Fragmentation, and Synthesis of β- d -Rhamnopyranosides and Other Deoxy Sugars
inferred← citeshttps://doi.org/10.1021/ol051038popenalex-snapshot
Efficient Installation of β-Mannosides Using a Dehydrative Coupling Strategy
inferred← citeshttps://doi.org/10.1021/ol301105yopenalex-snapshot
HPLC-Assisted Automated Oligosaccharide Synthesis
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Stereoselective tris-glycosylation to introduce β-(1→3)-branches into gentiotetraose for the concise synthesis of phytoalexin-elicitor heptaglucoside
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A novel liquid-phase strategy for organic synthesis using organic ions as soluble supports
inferred← citeshttps://doi.org/10.1039/c2ob06883dopenalex-snapshot
Direct O-glycosidation of resin bound thioglycosides
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Dehydrative glycosylation with cyclic phosphonium anhydrides
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The influence of acceptor nucleophilicity on the glycosylation reaction mechanism
inferred← citeshttps://doi.org/10.1039/c7cc00269fopenalex-snapshot
Regio- and stereoselective β-mannosylation using a boronic acid catalyst and its application in the synthesis of a tetrasaccharide repeating unit of lipopolysaccharide derived from E. coli O75
inferred← citeshttps://doi.org/10.1039/c8cs00905hopenalex-snapshot
Stereo- and regioselective glycosylation with protection-less sugar derivatives: an alluring strategy to access glycans and natural products
inferred← citeshttps://doi.org/10.1039/c9ob00670bopenalex-snapshot
Influence of remote functional groups towards the formation of 1,2- cis glycosides: special emphasis on β-mannosylation
inferred← citeshttps://doi.org/10.1039/d0ob01048kopenalex-snapshot
Synthesis of hyaluronic acid oligosaccharides with a GlcNAc–GlcA repeating pattern and their binding affinity with CD44
inferred← citeshttps://doi.org/10.1080/07328303.2017.1390579openalex-snapshot
Stereoselective β-mannosylation via anomeric O-Alkylation: Concise synthesis of β-D-Xyl-(l→2)-β-D-Man-(1→4)-α-D-Glc-OMe, a trisaccharide oligomer of the hyriopsis schlegelii glycosphingolipid
inferred← citeshttps://doi.org/10.1246/bcsj.77.169openalex-snapshot
6-Nitro-2-benzothiazolyl α-Glucoside and α-Mannoside in β-Selective Glycosylations
inferred← citeshttps://doi.org/10.1246/bcsj.79.479openalex-snapshot
6-Nitro-2-benzothiazolyl α-Mannoside: A Highly Efficient Mannosyl Donor in Constructing β-Man(1→4)GlcN Linkage and Its Application to the Synthesis of the Pentasaccharide Core of N-Glycans
inferred← citeshttps://doi.org/10.1246/cl.2003.442openalex-snapshot
Catalytic and β-Stereoselective Mannosylation of Several Glycosyl Acceptors with Mannosyl 6-Nitro-2-benzothiazoate
inferred← citeshttps://doi.org/10.2174/1385272822666181026115752openalex-snapshot
Recent Application of Polystyrene-supported Triphenylphosphine in Solid-Phase Organic Synthesis
inferred← citeshttps://doi.org/10.2174/138527282306190625103634openalex-snapshot
Recent Advances in Solid Phase Organic Synthesis (SPOS)
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inferred← citeshttps://doi.org/10.3390/m1111openalex-snapshot
Synthesis and Isolation of Diastereomeric Anomeric Sulfoxides from a d-Mannuronate Thioglycoside Building Block
inferred← citeshttps://doi.org/10.3390/molecules28155644openalex-snapshot
Recent Progress in 1,2-cis glycosylation for Glucan Synthesis
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