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Direct Synthesis of β-Mannopyranosides by the Sulfoxide Method
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Outgoing claims: the papers this work cites, builds on, or argues with.
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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On the Stereochemistry of Tethered Intermediates inp-Methoxybenzyl-Assisted β-Mannosylation
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inferred← citeshttps://doi.org/10.1016/s0040-4020(98)01202-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(99)01053-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00101-1openalex-snapshot
A concise route to the core pentasaccharide of N-linked glycoproteins
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)00124-5openalex-snapshot
Direct synthesis of β-d-Xyl-(1→2)-β-d-Man-(1→4)-α-d-Glc-OME: a trisaccharide component of the Hyriopsis schlegelii glycosphingolipid
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01163-0openalex-snapshot
A practical synthesis of β-d-mannopyranosides
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02159-5openalex-snapshot
Convergent, stereoselective synthesis of the caloporoside disaccharide
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)02209-1openalex-snapshot
Novel carbohydrate scaffolds. Assembly of a uridine–mannose scaffold based on tunicamycin
inferred← citeshttps://doi.org/10.1016/s0065-2318(04)59003-0openalex-snapshot
SYNTHESIS AND REACTIONS OF GLYCOSIDES
inferred← citeshttps://doi.org/10.1016/s0065-2318(09)00006-7openalex-snapshot
Chapter 6 Stereocontrolled Synthesis of Mannans and Rhamnans
inferred← citeshttps://doi.org/10.1016/s0304-4165(01)00164-7openalex-snapshot
A novel disaccharide substrate having 1,2-oxazoline moiety for detection of transglycosylating activity of endoglycosidases
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00487-5openalex-snapshot
A new glycosylation strategy for the synthesis of mannopyranosides
inferred← citeshttps://doi.org/10.1016/s0968-0896(97)00170-3openalex-snapshot
Synthesis of pavoninin-1, a shark repellent substance, and its structural analogues toward mechanistic studies on their membrane perturbation
inferred← citeshttps://doi.org/10.1016/s1874-5296(00)80015-7openalex-snapshot
Iodine, a versatile reagent in carbohydrate chemistry
inferred← citeshttps://doi.org/10.1021/acs.accounts.6b00164openalex-snapshot
Twenty Years of Mycobacterial Glycans: Furanosides and Beyond
inferred← citeshttps://doi.org/10.1021/acs.chemrev.2c00892openalex-snapshot
Catalytic Approaches to Chemo- and Site-Selective Transformation 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.chemrev.8b00083openalex-snapshot
The Experimental Evidence in Support of Glycosylation Mechanisms at the SN1–SN2 Interface
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00402openalex-snapshot
Total Synthesis of Phospholipomannan of Candida albicans
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01834openalex-snapshot
Synthetic Carbohydrate Chemistry and Translational Medicine
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02045openalex-snapshot
Conformationally Constrained Glycosyl Donors as Tools to Control Glycosylation Outcomes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01535openalex-snapshot
Influence of Configuration at the 4- and 6-Positions on the Conformation and Anomeric Reactivity and Selectivity of 7-Deoxyheptopyranosyl Donors: Discovery of a Highly Equatorially Selective l -glycero- d -gluco-Heptopyranosyl Donor
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00140openalex-snapshot
Construction of β-Mannosidic Bonds via Gold(I)-Catalyzed Glycosylations with Mannopyranosyl ortho-Hexynylbenzoates and Its Application in Synthesis of Acremomannolipin A
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01978openalex-snapshot
Mechanism of 3-O-Acyl-Directed α-Mannopyranosylation and Rationalization of the Contrasting Behavior of 3-O-Acyl Glucopyranosyl Donors
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02106openalex-snapshot
Chemical Synthesis of a Complex-Type N-Glycan Containing a Core Fucose
inferred← citeshttps://doi.org/10.1021/acs.joc.6b03017openalex-snapshot
Deactivating Influence of 3-O-Glycosyl Substituent on Anomeric Reactivity of Thiomannoside Observed in Oligomannoside Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00101openalex-snapshot
Total Synthesis of Tiacumicin A. Total Synthesis, Relay Synthesis, and Degradation Studies of Fidaxomicin (Tiacumicin B, Lipiarmycin A3)
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04363openalex-snapshot
Direct β-Mannosylation of Primary Alcohol Acceptors: Trisaccharide Iteration Assembly of β-1,6-Oligomannosides Corresponding to Kakelokelose
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03256openalex-snapshot
ZnI 2 -Mediated β-Galactosylation of C2-Ether-Type Donor
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01602openalex-snapshot
Total Synthesis of the Glycosylated Macrolide Antibiotic Fidaxomicin
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00926openalex-snapshot
Glycosyl-Acceptor-Derived Borinic Ester-Promoted Direct and β-Stereoselective Mannosylation with a 1,2-Anhydromannose Donor
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/acscentsci.3c00896openalex-snapshot
Phosphates as Assisting Groups in Glycan Synthesis
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.8b00413openalex-snapshot
Synthesis of 12-O-Mono- and Diglycosyl-oxystearates, a New Class of Agonists for the C-type Lectin Receptor Mincle
inferred← citeshttps://doi.org/10.1021/ar100035ropenalex-snapshot
Mechanism of a Chemical Glycosylation Reaction
inferred← citeshttps://doi.org/10.1021/bk-2012-1102.ch010openalex-snapshot
Systematic Synthesis of Aminosugars and Their Stereoselective Glycosylation
inferred← citeshttps://doi.org/10.1021/cr100444bopenalex-snapshot
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
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/ja029302mopenalex-snapshot
2,3-Anhydro Sugars in Glycoside Bond Synthesis. Highly Stereoselective Syntheses of Oligosaccharides Containing α- and β-Arabinofuranosyl Linkages
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/ja4056678openalex-snapshot
‘Naked’ and Hydrated Conformers of the Conserved Core Pentasaccharide of N-linked Glycoproteins and Its Building Blocks
inferred← citeshttps://doi.org/10.1021/ja405990zopenalex-snapshot
Chemical Synthesis of Highly Congested gp120 V1V2 N-Glycopeptide Antigens for Potential HIV-1-Directed Vaccines
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/ja710935zopenalex-snapshot
Stereoselective Direct Glycosylation with Anomeric Hydroxy Sugars by Activation with Phthalic Anhydride and Trifluoromethanesulfonic Anhydride Involving Glycosyl Phthalate Intermediates
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/ja980827hopenalex-snapshot
Sulfenate Intermediates in the Sulfoxide Glycosylation Reaction
inferred← citeshttps://doi.org/10.1021/jacs.0c03215openalex-snapshot
Stereocontrolled Synthesis of the Equatorial Glycosides of 3-Deoxy- d -manno-oct-2-ulosonic Acid: Role of Side Chain Conformation
inferred← citeshttps://doi.org/10.1021/jacs.0c04255openalex-snapshot
Highly Selective β-Mannosylations and β-Rhamnosylations Catalyzed by Bis-thiourea
inferred← citeshttps://doi.org/10.1021/jacs.0c05592openalex-snapshot
Glycoside Hydrolases Restrict the Side Chain Conformation of Their Substrates To Gain Additional Transition State Stabilization
inferred← citeshttps://doi.org/10.1021/jacs.5b12528openalex-snapshot
Studies of the Mechanism and Origins of Enantioselectivity for the Chiral Phosphoric Acid-Catalyzed Stereoselective Spiroketalization Reactions
inferred← citeshttps://doi.org/10.1021/jacs.6b08874openalex-snapshot
β-Stereoselective Mannosylation Using 2,6-Lactones
inferred← citeshttps://doi.org/10.1021/jacs.7b03198openalex-snapshot
Regiodivergent Glycosylations of 6-Deoxy-erythronolide B and Oleandomycin-Derived Macrolactones Enabled by Chiral Acid Catalysis
inferred← citeshttps://doi.org/10.1021/jacsau.5c01069openalex-snapshot
Commonality of Mechanism in Glycoside Hydrolases, Nucleoside Hydrolases, and Phosphorylases: Importance of Side-Chain Conformation Preorganization
inferred← citeshttps://doi.org/10.1021/jo0005870openalex-snapshot
A Highly Stereoselective Construction of β-Glycosyl Linkages by Reductive Cleavage of Cyclic Sugar Ortho Esters
inferred← citeshttps://doi.org/10.1021/jo0108818openalex-snapshot
Synthesis of the Salmonella Type E1 Core Trisaccharide as a Probe for the Generality of 1-(Benzenesulfinyl)piperidine/Triflic Anhydride Combination for Glycosidic Bond Formation from Thioglycosides
inferred← citeshttps://doi.org/10.1021/jo010910eopenalex-snapshot
Arabinofuranosides from Mycobacteria: Synthesis of a Highly Branched Hexasaccharide and Related Fragments Containing β-Arabinofuranosyl Residues
inferred← citeshttps://doi.org/10.1021/jo026519qopenalex-snapshot
Highly Diastereoselective Oxidation of 2-Amino-2-deoxy-1-thio-β- d -glucopyranosides: Synthesis of Imino Sulfinylglycosides
inferred← citeshttps://doi.org/10.1021/jo035698oopenalex-snapshot
Selective Oxidation of Glycosyl Sulfides to Sulfoxides Using Magnesium Monoperoxyphthalate and Microwave Irradiation
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/jo302455dopenalex-snapshot
Influence of O6 in Mannosylations Using Benzylidene Protected Donors: Stereoelectronic or Conformational Effects?
inferred← citeshttps://doi.org/10.1021/jo801414copenalex-snapshot
Block Synthesis of Tetra- and Hexasaccharides (β- d -Glycero- d -manno-Hepp-(1→4)-[α- l -Rhap-(1→3)-β- d -glycero- d -manno-Hepp-(1→4)]n-α- l -Rhap-OMe (n = 1 and 2)) Corresponding to Multiple Repeat Units of the Glycan from the Surface-Layer Glycoprotein from Bacillus thermoaerophilus
inferred← citeshttps://doi.org/10.1021/jo8019835openalex-snapshot
Sonication-Assisted Oligomannoside Synthesis
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/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/jo900026eopenalex-snapshot
The 4-(tert-Butyldiphenylsiloxy)-3-fluorobenzyl Group: A New Alcohol Protecting Group, Fully Orthogonal with the p-Methoxybenzyl Group and Removable under Desilylation Conditions
inferred← citeshttps://doi.org/10.1021/jo900662vopenalex-snapshot
Stereodirecting Effect of the Pyranosyl C-5 Substituent in Glycosylation Reactions
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/jo971778eopenalex-snapshot
Glycosylation Reactions with a (4-Alkoxypentadienyl)oxy Leaving Group Linking the Glycosyl Donor and the Acceptor Moiety
inferred← citeshttps://doi.org/10.1021/jo971934hopenalex-snapshot
Novel Bicylic Donors for the Synthesis of 2-Deoxy-β-Glycosides
inferred← citeshttps://doi.org/10.1021/jo990243dopenalex-snapshot
Chemistry of 4,6-O-Benzylidene- d -glycopyranosyl Triflates: Contrasting Behavior between the Gluco and Manno Series
inferred← citeshttps://doi.org/10.1021/jo9910482openalex-snapshot
Highly Diastereoselective α-Mannopyranosylation in the Absence of Participating Protecting Groups
inferred← citeshttps://doi.org/10.1021/jo9914667openalex-snapshot
Direct Stereoselective Synthesis of β-Thiomannosides
inferred← citeshttps://doi.org/10.1021/ol026629jopenalex-snapshot
Synthesis of α-Glucuronic Acid and Amide Derivatives in the Presence of a Participating 2-Acyl Protecting Group
inferred← citeshttps://doi.org/10.1021/ol300634xopenalex-snapshot
Strict Stereocontrol by 2,4-O-Di-tert-butylsilylene Group on β-Glucuronylations
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/ol801190copenalex-snapshot
Highly Direct α-Selective Glycosylations of 3,4-O-Carbonate-Protected 2-Deoxy- and 2,6-Dideoxythioglycosides by Preactivation Protocol
inferred← citeshttps://doi.org/10.1021/ol801710sopenalex-snapshot
Studies on the Stereoselective Synthesis of C-Allyl Glycosides
inferred← citeshttps://doi.org/10.1021/op900084fopenalex-snapshot
Renaissance of Traditional Organic Reactions under Microfluidic Conditions: A New Paradigm for Natural Products Synthesis
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