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ortho -Methoxycarbonylethynylphenyl Thioglycosides (MCEPTs): Versatile Glycosyl Donors Enabled by Electron-Withdrawing Substituents and Catalyzed by Gold(I) or Cu(II) Complexes

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Carbohydrates in Chemistry and Biology

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Direct and Stereoselective Synthesis of 2‐Acetamido‐2‐deoxy‐β‐ D ‐glycopyranosides by Using the Phosphite Method

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Advances in Selective Chemical Syntheses of Complex Oligosaccharides

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New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]

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Protein Posttranslational Modifications: The Chemistry of Proteome Diversifications

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New Principles for Glycoside‐Bond Formation

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Chemical Synthesis and Antigenic Evaluation of Inner Core Oligosaccharides from Acinetobacter baumannii Lipopolysaccharide

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Gold(I)‐Catalyzed Glycosylation with Glycosyl ortho ‐Alkynylbenzoates as Donors: General Scope and Application in the Synthesis of a Cyclic Triterpene Saponin

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Uronic Acids in Oligosaccharide Synthesis

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Medical uses of gold compounds: Past, present and future

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Aromatic O-glycosylation

inferredcites →https://doi.org/10.1016/j.carres.2014.06.009openalex-snapshot

Thioglycosides in Carbohydrate Research

inferredcites →https://doi.org/10.1016/j.carres.2015.02.007openalex-snapshot

Common side reactions of the glycosyl donor in chemical glycosylation

inferredcites →https://doi.org/10.1016/j.carres.2015.10.001openalex-snapshot

Surface polysaccharides from Acinetobacter baumannii : Structures and syntheses

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ortho-Alkynylphenyl thioglycosides as a new type of glycosylation donors under the catalysis of Au(I) complexes

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“Active” and “latent” thioglycosyl donors in oligosaccharide synthesis. Application to the synthesis of α-sialosides

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Di-tert-butylsilylene (DTBS) group-directed α-selective galactosylation unaffected by C-2 participating functionalities

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Chapter 5 Oligosaccharide Synthesis: From Conventional Methods to Modern Expeditious Strategies

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Gold(I)-Catalyzed Glycosylation with Glycosyl o -Alkynylbenzoates as Donors

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Methods for 2-Deoxyglycoside Synthesis

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“One-Pot” Protection, Glycosylation, and Protection–Glycosylation Strategies of Carbohydrates

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Catalytic Glycosylations in Oligosaccharide Synthesis

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Chemoenzymatic Methods for the Synthesis of Glycoproteins

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Diversity-Oriented Synthesis of Steviol Glycosides

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8-(Methyltosylaminoethynyl)-1-naphthyl (MTAEN) Glycosides: Potent Donors in Glycosides Synthesis

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GeCl2·Dioxane–AgBF4 Catalyzed Activation of Glycosyl Fluorides for Glycosylation

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Gallium(III)-Promoted Halocyclizations of 1,6-Diynes

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A Highly Efficient Approach To Construct (epi)-Podophyllotoxin-4-O-glycosidic Linkages as well as Its Application in Concise Syntheses of Etoposide and Teniposide

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MPTGs: Thioglycoside Donors for Acid-Catalyzed O-Glycosylation and Latent-Active Synthetic Strategies

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Recent progress in O-glycosylation methods and its application to natural products synthesis

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Formation and Structure of Self-Assembled Monolayers

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Gold-Catalyzed Synthesis of 2-Deoxy Glycosides Using S -But-3-ynyl Thioglycoside Donors

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Efficient Stereoselective Synthesis of γ- N -Glycosyl Asparagines by N-Glycosylation of Primary Amide Groups

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Mechanistic Insights into the Gold(I)-Catalyzed Activation of Glycosyl ortho -Alkynylbenzoates for Glycosidation

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o -( p -Methoxyphenylethynyl)phenyl Glycosides: Versatile New Glycosylation Donors for the Highly Efficient Construction of Glycosidic Linkages

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Glycosylation with 3,5-Dimethyl-4-(2′-phenylethynylphenyl)phenyl (EPP) Glycosides via a Dearomative Activation Mechanism

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Palladium-Catalyzed Arylation of Enynes and Electron-Deficient Alkynes Using Diaryliodonium Salts

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Halogen-bond-assisted radical activation of glycosyl donors enables mild and stereoconvergent 1,2-cis-glycosylation

inferredcites →https://doi.org/10.1038/s44160-022-00171-9openalex-snapshot

Automated solution-phase multiplicative synthesis of complex glycans up to a 1,080-mer

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ortho-(Methyltosylaminoethynyl)benzyl glycosides as new glycosyl donors for latent-active glycosylation

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Glycosylation, an effective synthetic strategy to improve the bioavailability of therapeutic peptides

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Fluorine-directed 1,2-trans glycosylation of rare sugars

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Hydrogen bond activated glycosylation under mild conditions

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Transesterification of α-Amino Esters Catalyzed by a Tetranuclear Zinc Cluster: Zn4(OCOCF3)6O

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Acinetobacter baumannii : evolution of a global pathogen

inferredcites →https://doi.org/10.1134/s0006297909110170openalex-snapshot

Glycoscience. Chemistry and chemical biology

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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PIFA‐Mediated C─H Thiolation and Selenylation of Pseudo ‐Anomeric Position of Glycals with Disulfides or Diselenides at Room Temperature

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Stereoselective Synthesis of the O‐antigen of A. baumannii ATCC 17961 Using Long‐Range Levulinoyl Group Participation

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A Radical Activation Strategy for Versatile and Stereoselective N‐Glycosylation

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Stereoselective P(III)‐Glycosylation for the Preparation of Phosphinated Sugars

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Stereoselective Synthesis of the O‐antigen of A. baumannii ATCC 17961 Using Long‐Range Levulinoyl Group Participation

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A Radical Activation Strategy for Versatile and Stereoselective N‐Glycosylation

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Stereoselective P(III)‐Glycosylation for the Preparation of Phosphinated Sugars

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Radical Strategy Towards N ‐glycosides: Current Advances and Future Prospects

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1‐(2’‐Hydroxy‐2’‐Methylpropionyl)Glycoside as a Versatile Glycosyl Donor for O ‐/ C ‐Glycosylation

inferred← citeshttps://doi.org/10.1002/cjoc.202400121openalex-snapshot

Stereoselective α‐Glycosylation with GlcN3 Donors Enabled Collective Syntheses of Acinetobacter baumannii Capsular Polysaccharides K43 , K47 and K88 Repeating Units†

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Stereoselective Synthesis of 2‐Deoxy Glycosides via a Novel 2‐O‐Resided (o‐Alkynyl)benzoate‐Initiated 1,2‐Sulfur Migration/Glycosylation and Desulfurization Protocol as well as Mechanism Elucidation

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Recent Advances of Carbohydrate‐Based Vaccines Against Acinetobacter baumannii

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Trendbericht Organische Chemie 2024

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Chemical Synthesis of Complex Carbohydrates

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Synthesis of aryl thioglycosides by metal-free arylation of glycosyl thiols with diaryliodonium salts under basic conditions

inferred← citeshttps://doi.org/10.1016/j.carres.2025.109639openalex-snapshot

Synthesis of disaccharide and trisaccharide substructures of an A. baumannii lipooligosaccharide core

inferred← citeshttps://doi.org/10.1016/j.carres.2026.110125openalex-snapshot

Recent Advances in Anomeric C-S Bond Activation: Emerging Opportunities for Stereoselective Glycosides

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Catalytic ring-strain release toward a facial and efficient synthesis of versatile C-glycosides

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Unraveling chemical glycosylation: DFT insights into factors imparting stereoselectivity

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Stereoselective AromaticO-Glycosylation of Glycosyl Chloride with Arylboronic Acid under an Air Atmosphere

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Reaction Rate and Stereoselectivity Enhancement in Glycosidations with O-Glycosyl Trihaloacetimidate Donors due to Catalysis by a Lewis Acid–Nitrile Cooperative Effect

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Highly Reactive Glycosylation with 1-O-(Methylthio)thiocarbonyl Glycosyl Donors under Acidic to Neutral Reaction Conditions

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Insertion of Glycosylidene Carbenes into Phenolic O–H Bonds for the Synthesis of O -Aryl Glycosides

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Synthesis of Disarmed (Alkylthio)carbonyl Glycosyl Donors and Comparison of Their Glycosylation Reactions.

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Chemical Glycosylation with p -Methoxyphenyl (PMP) Glycosides via Oxidative Activation

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A Cu(OTf) 2 -Catalyzed Glycosylation with Glycosyl ortho - N -Phthalimidoylpropynyl Benzoates as Donors

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S - o -( p -Methoxyphenylethynyl)benzyl (SMPEB) Glycosides for Catalytic Glycosylation and Their Application in the Synthesis of Polyporus Umbellatus Polysaccharides

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Palladium-Catalyzed O -Glycosylation through π–π Interactions

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N -( para -Methoxyphenylpropargyl) Pyrrole-2-carboxylate (PPPC) Glycosides as Donors for Glycosylation

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Total Synthesis of Kasugamycin

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Copper-Catalyzed Glycosylation Protocol Based on 1,4-Naphthoquinone-Derived Thioglycosides

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Electrochemical 2-Deoxyglycosylation of N -Containing Molecules with β-Stereoselectivity

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Reactivity Tuning by Ring Size: A Glycosylation Protocol Using Thiophene-Scaffolded Glycosyl Donors

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NiCl 2 /Hdipm-Catalyzed 2-OH-Selective Alkylation of Glycoside trans -Diols

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A Photoacid-Assisted Ag(I)-Catalyzed Glycosylation Based on ortho -Methoxycarbonylethynylphenyl Thioglycosides

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Cellobiose-Derived β-Linked Disaccharide Donor Enables Convergent Syntheses of Acinetobacter baumannii K91 and K25 Capsular Trisaccharides

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Thiourea-Catalyzed, Hypervalent Iodine-Assisted Deoxygenative or Desulfurative Amidation of Alcohols

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2-Alkynyl-1-Naphthoate: A Reactive and Base-Tolerant Leaving Group for Gold(I)-Catalyzed Glycosylation

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Sterically Congested 2,2-Dimethylphenylacetate Glycosyl Donors for Versatile Protecting-Group Manipulations and Orthogonal Glycosylations

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Iridium Photoredox-Catalyzed Stereoselective C-Glycosylation with Tetrafluoropyridin-4-yl Thioglycosides: A Facile Synthesis of C-α/β-Glucogallins and Their Antioxidant Activity

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Site-Switchable Alkylation of Carbohydrates Controlled by Inexpensive Metal Ion Catalysts

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Copper-Catalyzed Photocatalyst-Free Radical N -Glycosylation

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Catalyst-free and wavelength-tuned glycosylation based on excited-state intramolecular proton transfer

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Thiourea-Cu(OTf) 2 /NIS-synergistically promoted stereoselective glycoside formation with 2-azidoselenoglycosides or thioglycosides as donors

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Nitrene-mediated glycosylation with thioglycoside donors under metal catalysis

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Para -(3-phenylpropiolamido)phenyl (PPAP) glycosides: Harnessing ipso -cyclization–driven glycosylation for strategic flexibility

inferred← citeshttps://doi.org/10.1126/science.adk1111openalex-snapshot

Palladium catalysis enables cross-coupling–like S N 2-glycosylation of phenols

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Catalytic Thioglycoside Activation with Diazo-Derived Copper Carbenes

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Regio- and Stereo-selective Synthesis of 1β-/3R-Aryl Thiosugar

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