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Electrochemical Generation of Glycosyl Triflate Pools
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Basic Concepts of “Cation Pool” and “Cation Flow” Methods and Their Applications in Conventional and Combinatorial Organic Synthesis
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Chemoselective Iterative Dehydrative Glycosylation
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Electroauxiliary‐Assisted Sequential Introduction of Two Carbon Nucleophiles on the Same α‐Carbon of Nitrogen: Application to the Synthesis of Spiro Compounds.
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The methanolysis of some derivatives of 2,3,4-tri-O-benzyl-α-D-glucopyranosyl bromide in the presence and absence of silver salts
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00036openalex-snapshot
“One-Pot” Protection, Glycosylation, and Protection–Glycosylation Strategies of Carbohydrates
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.joc.0c00292openalex-snapshot
Unified Strategy toward Stereocontrolled Assembly of Various Glucans Based on Bimodal Glycosyl Donors
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01065openalex-snapshot
Tf2O-Promoted Regioselective Heteronucleophilic Ring-Opening Approaches of Tetrahydrofuran
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02207openalex-snapshot
Exploiting the Strained Ion-Pair Interactions of Sterically Hindered Pyridinium Salts Toward SN2 Glycosylation of Glycosyl Trichloroacetimidates
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01067openalex-snapshot
Triflic Anhydride-Mediated Approach to Furo[3,2-b]furans from Diacetonide Protected Furanoses
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01423openalex-snapshot
Triflic Anhydride-Mediated Unprecedented Reactivities of Diacetonide Endoglucofuranose and Ribose Tetracetate: Direct Access to γ-Butenolides and Oxazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00047openalex-snapshot
2-O-N-Benzylcarbamoyl as a Protecting Group To Promote β-Selective Glycosylation and Its Applications in the Stereoselective Synthesis of Oligosaccharides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00406openalex-snapshot
Automated Electrochemical Assembly of the Protected Potential TMG-chitotriomycin Precursor Based on Rational Optimization of the Carbohydrate Building Block
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02823openalex-snapshot
Photoinduced C–S Bond Cleavage of Thioglycosides and Glycosylation
inferred← citeshttps://doi.org/10.1021/acscatal.4c02322openalex-snapshot
Electrochemical Glycosylation via Halogen-Atom-Transfer for C -Glycoside Assembly
inferred← citeshttps://doi.org/10.1021/ar100035ropenalex-snapshot
Mechanism of a Chemical Glycosylation Reaction
inferred← citeshttps://doi.org/10.1021/cr0680843openalex-snapshot
Modern Strategies in Electroorganic Synthesis
inferred← citeshttps://doi.org/10.1021/cr500434xopenalex-snapshot
Mechanisms of Glycosylation Reactions Studied by Low-Temperature Nuclear Magnetic Resonance
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/ja306663gopenalex-snapshot
Polymer-Bound Pyrene-4,5,9,10-tetraone for Fast-Charge and -Discharge Lithium-Ion Batteries with High Capacity
inferred← citeshttps://doi.org/10.1021/ja905008popenalex-snapshot
Equatorial Anomeric Triflates from Mannuronic Acid Esters
inferred← citeshttps://doi.org/10.1021/ja907252uopenalex-snapshot
β-Directing Effect of Electron-Withdrawing Groups at O-3, O-4, and O-6 Positions and α-Directing Effect by Remote Participation of 3-O-Acyl and 6-O-Acetyl Groups of Donors in Mannopyranosylations
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.6b06943openalex-snapshot
Borinic Acid Catalyzed Stereo- and Regioselective Couplings of Glycosyl Methanesulfonates
inferred← citeshttps://doi.org/10.1021/jacs.6c00007openalex-snapshot
Stereo-Switchable Electrochemical Glycosylation
inferred← citeshttps://doi.org/10.1021/jo2017026openalex-snapshot
Methodology Development and Physical Organic Chemistry: A Powerful Combination for the Advancement of Glycochemistry
inferred← citeshttps://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?
inferred← citeshttps://doi.org/10.1021/jo500032kopenalex-snapshot
Glycosyl Dithiocarbamates: β-Selective Couplings without Auxiliary Groups
inferred← citeshttps://doi.org/10.1021/jo801462ropenalex-snapshot
Installation of Electron-Donating Protective Groups, a Strategy for Glycosylating Unreactive Thioglycosyl Acceptors using the Preactivation-Based Glycosylation Method
inferred← citeshttps://doi.org/10.1021/jo801551ropenalex-snapshot
How the Arming Participating Moieties can Broaden the Scope of Chemoselective Oligosaccharide Synthesis by Allowing the Inverse Armed−Disarmed Approach
inferred← citeshttps://doi.org/10.1021/jo8020192openalex-snapshot
The Stereodirecting Effect of the Glycosyl C5-Carboxylate Ester: Stereoselective Synthesis of β-Mannuronic Acid Alginates
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/ol200242uopenalex-snapshot
Glycosyl Sulfonium Ions as Storable Intermediates for Glycosylations
inferred← citeshttps://doi.org/10.1021/ol302941qopenalex-snapshot
Visible Light Mediated Activation and O-Glycosylation of Thioglycosides
inferred← citeshttps://doi.org/10.1021/ol402034gopenalex-snapshot
Automated Solution-Phase Synthesis of Oligosaccharides via Iterative Electrochemical Assembly of Thioglycosides
inferred← citeshttps://doi.org/10.1021/ol4026342openalex-snapshot
Development of Glycosylation Using the Glucopyranose 1,2-Orthobenzoate under Electrochemical Conditions
inferred← citeshttps://doi.org/10.1039/b813048eopenalex-snapshot
Thio-arylglycosides with various aglyconpara-substituents: a probe for studying chemical glycosylation reactions
inferred← citeshttps://doi.org/10.1039/bk9781837672844-00044openalex-snapshot
Enabling technologies applied to glycosylation
inferred← citeshttps://doi.org/10.1039/bk9781849733274-00072openalex-snapshot
Nucleophilic Substitution at the Anomeric Centre
inferred← citeshttps://doi.org/10.1039/c4ob01807aopenalex-snapshot
Strained olefin enables triflic anhydride mediated direct dehydrative glycosylation
inferred← citeshttps://doi.org/10.1039/c6sc00633gopenalex-snapshot
A versatile glycosylation strategy via Au( iii ) catalyzed activation of thioglycoside donors
inferred← citeshttps://doi.org/10.1039/d0ob00373eopenalex-snapshot
1,2- cis -Selective glucosylation enabled by halogenated benzyl protecting groups
inferred← citeshttps://doi.org/10.1039/d1ob02115jopenalex-snapshot
Electrocatalysis as a key strategy for the total synthesis of natural products
inferred← citeshttps://doi.org/10.1039/d2cc02344jopenalex-snapshot
Rapid access to organic triflates based on flash generation of unstable sulfonium triflates in flow
inferred← citeshttps://doi.org/10.1039/d4cc00142gopenalex-snapshot
Electrochemical desulfurative formation of C–N bonds through selective activation of inert C(sp 3 )–S bonds
inferred← citeshttps://doi.org/10.1039/d6cc05492gopenalex-snapshot
Electrochemical glycosylation using o -[1-( p -MeO-phenyl)vinyl]benzoates (PMPVB) as glycosylation donors
inferred← citeshttps://doi.org/10.1080/07328303.2010.508141openalex-snapshot
Neighboring Group Participation in Glycosylation Reactions by 2,6-Disubstituted 2- O -Benzoyl groups: A Mechanistic Investigation
inferred← citeshttps://doi.org/10.1139/v08-128openalex-snapshot
Synthesis and properties of end-capped bis(oligothienyl) sulfides
inferred← citeshttps://doi.org/10.1246/bcsj.20150100openalex-snapshot
Reaction Integration Using Electrogenerated Cationic Intermediates
inferred← citeshttps://doi.org/10.1246/cl.170126openalex-snapshot
Synthesis of a TMG-chitotriomycin Precursor Based on Electrolyte-free Electrochemical Glycosylation Using an Ionic Liquid Tag
inferred← citeshttps://doi.org/10.1246/cl.2008.942openalex-snapshot
Oligosaccharide Synthesis Based on a One-pot Electrochemical Glycosylation–Fmoc Deprotection Sequence
inferred← citeshttps://doi.org/10.1246/cl.2011.678openalex-snapshot
Electrochemically Generated ArS(ArSSAr)+B(C6F5)4− as an Activator of Thioglycosides for Glycosylation
inferred← citeshttps://doi.org/10.2147/roc.s32147openalex-snapshot
A study of silver (I) perchlorate as an effective promoter for chemical glycosylation with thioimidates and thioglycosides
inferred← citeshttps://doi.org/10.3390/molecules30183693openalex-snapshot
Microwave-Assisted Neutral Glycosylation Reactions in the Absence of Reagent Activators
inferred← citeshttps://doi.org/10.3762/bjoc.13.195openalex-snapshot
1,3-Dibromo-5,5-dimethylhydantoin as promoter for glycosylations using thioglycosides
inferred← citeshttps://doi.org/10.3762/bjoc.13.207openalex-snapshot
Preactivation-based chemoselective glycosylations: A powerful strategy for oligosaccharide assembly
inferred← citeshttps://doi.org/10.3762/bjoc.13.93openalex-snapshot
Total synthesis of TMG-chitotriomycin based on an automated electrochemical assembly of a disaccharide building block
inferred← citeshttps://doi.org/10.3762/bjoc.18.117openalex-snapshot
Synthesis of protected precursors of chitin oligosaccharides by electrochemical polyglycosylation of thioglycosides
inferred← citeshttps://doi.org/10.3762/bjoc.8.52openalex-snapshot
Electrochemical generation of 2,3-oxazolidinone glycosyl triflates as an intermediate for stereoselective glycosylation
inferred← citeshttps://doi.org/10.4052/tigg.20.175openalex-snapshot
Electrochemical Conversion of Thioglycosides to Glycosyl Triflates
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.71.1136openalex-snapshot
Recent Developments in the ^|^ldquo;Cation Pool^|^rdquo; Method
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.71.616openalex-snapshot
Unique Reactivity of Pyranosides with 2,3-trans Carbamate Group; Renaissance of Endocyclic Cleavage Reaction
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.72.797openalex-snapshot
Recent Progress of Chemical Glycosylations and Oligosaccharide Synthesis
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.79.839openalex-snapshot
Synthesis of Oligosaccharides of Glucosamine by Automated Electrochemical Assembly
inferred← citeshttps://doi.org/10.5796/electrochemistry.25-00104openalex-snapshot
New Concept of Capillary Covered Carbon Felt Electrodes. Application to Electro-organic Synthesis in Small Scale
inferred← citeshttps://doi.org/10.5796/electrochemistry.25-00142openalex-snapshot
Generation and Reaction of Benzyl Triflates by Anodic Oxidation of Toluenes
inferred← citeshttps://doi.org/10.58837/chula.the.2018.104openalex-snapshot
Glycosylation of Thioglycosides with Bromodiethylsulfonium bromopentachloroantimonate as novel activator
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