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Catalyst-Controlled Stereoselective O-Glycosylation: Pd(0) vs Pd(II)

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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/anie.200802036openalex-snapshot
New Principles for Glycoside‐Bond Formation
inferredcites →https://doi.org/10.1002/anie.201100514openalex-snapshot
An Efficient Approach to the Synthesis of Nucleosides: Gold(I)‐Catalyzed N‐Glycosylation of Pyrimidines and Purines with Glycosyl ortho ‐Alkynyl Benzoates
inferredcites →https://doi.org/10.1002/anie.201103409openalex-snapshot
Characterization of the Isochromen‐4‐yl‐gold(I) Intermediate in the Gold(I)‐Catalyzed Glycosidation of Glycosyl ortho‐Alkynylbenzoates and Enhancement of the Catalytic Efficiency Thereof
inferredcites →https://doi.org/10.1002/anie.201210266openalex-snapshot
Stereoselective β‐C‐Glycosylation by a Palladium‐Catalyzed Decarboxylative Allylation: Formal Synthesis of Aspergillide A
inferredcites →https://doi.org/10.1002/anie.201403754openalex-snapshot
Palladium‐Catalyzed Decarboxylative Cycloaddition of Vinylethylene Carbonates with Formaldehyde: Enantioselective Construction of Tertiary Vinylglycols
inferredcites →https://doi.org/10.1002/anie.201407013openalex-snapshot
Palladium‐Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with Michael Acceptors: Construction of Vicinal Quaternary Stereocenters
inferredcites →https://doi.org/10.1002/anie.201408739openalex-snapshot
Reversing the Stereoselectivity of a Palladium‐Catalyzed O‐Glycosylation through an Inner‐Sphere or Outer‐Sphere Pathway
inferredcites →https://doi.org/10.1002/anie.201507861openalex-snapshot
Interrupted Pummerer Reaction in Latent‐Active Glycosylation: Glycosyl Donors with a Recyclable and Regenerative Leaving Group
inferredcites →https://doi.org/10.1002/anie.201600142openalex-snapshot
Stereoselective Koenigs–Knorr Glycosylation Catalyzed by Urea
inferredcites →https://doi.org/10.1002/anie.201612071openalex-snapshot
Palladium‐Catalyzed Direct Stereoselective Synthesis of Deoxyglycosides from Glycals
inferredcites →https://doi.org/10.1002/chem.200902548openalex-snapshot
Gold(I)‐Catalyzed Glycosylation with Glycosyl ortho ‐Alkynylbenzoates as Donors: General Scope and Application in the Synthesis of a Cyclic Triterpene Saponin
inferredcites →https://doi.org/10.1002/chem.201301871openalex-snapshot
Design of Glycosyltransferase Inhibitors: Pyridine as a Pyrophosphate Surrogate
inferredcites →https://doi.org/10.1002/chem.201303241openalex-snapshot
β‐Type Glycosidic Bond Formation by Palladium‐Catalyzed Decarboxylative Allylation
inferredcites →https://doi.org/10.1002/ejoc.201200242openalex-snapshot
Palladium‐Catalyzed Improved Regio‐ and Stereoselective O‐Glycosylation of D ‐Glucal‐Derived β‐ and α‐Vinyl Oxiranes
inferredcites →https://doi.org/10.1002/ejoc.201600484openalex-snapshot
Glycosylation via Transition‐Metal Catalysis: Challenges and Opportunities
inferredcites →https://doi.org/10.1021/acs.chemrev.5b00163openalex-snapshot
Computational Studies of Synthetically Relevant Homogeneous Organometallic Catalysis Involving Ni, Pd, Ir, and Rh: An Overview of Commonly Employed DFT Methods and Mechanistic Insights
inferredcites →https://doi.org/10.1021/cr1002744openalex-snapshot
Transition Metal-Catalyzed Decarboxylative Allylation and Benzylation Reactions
inferredcites →https://doi.org/10.1021/cr9409804openalex-snapshot
Asymmetric Transition Metal-Catalyzed Allylic Alkylations
inferredcites →https://doi.org/10.1021/cr9902704openalex-snapshot
Ligand Bite Angle Effects in Metal-catalyzed C−C Bond Formation
inferredcites →https://doi.org/10.1021/cr990307kopenalex-snapshot
Intramolecular O-Glycoside Bond Formation
inferredcites →https://doi.org/10.1021/cs3002513openalex-snapshot
Recent Advances in Transition Metal-Catalyzed Glycosylation
inferredcites →https://doi.org/10.1021/ja010086bopenalex-snapshot
Why Are the Hydroxy Groups of Partially Protected N-Acetylglucosamine Derivatives Such Poor Glycosyl Acceptors, and What Can Be Done about It? A Comparative Study of the Reactivity of N-Acetyl-, N-Phthalimido-, and 2-Azido-2-deoxy-glucosamine Derivatives in Glycosylation. 2-Picolinyl Ethers as…
inferredcites →https://doi.org/10.1021/ja0347538openalex-snapshot
De Novo Asymmetric Bio- and Chemocatalytic Synthesis of Saccharides − Stereoselective Formal O-Glycoside Bond Formation Using Palladium Catalysis
inferredcites →https://doi.org/10.1021/ja037097kopenalex-snapshot
A Palladium-Catalyzed Glycosylation Reaction: The de Novo Synthesis of Natural and Unnatural Glycosides
inferredcites →https://doi.org/10.1021/ja039400nopenalex-snapshot
De Novo Synthesis of Oligosaccharides Using a Palladium-Catalyzed Glycosylation Reaction
inferredcites →https://doi.org/10.1021/ja039746yopenalex-snapshot
Stereoselective Palladium-Catalyzed O-Glycosylation Using Glycals
inferredcites →https://doi.org/10.1021/ja052548hopenalex-snapshot
A General Strategy for Stereoselective Glycosylations
inferredcites →https://doi.org/10.1021/ja3018187openalex-snapshot
Stereoselective Assembly of Complex Oligosaccharides Using Anomeric Sulfonium Ions as Glycosyl Donors
inferredcites →https://doi.org/10.1021/ja307355nopenalex-snapshot
Effect of Remote Picolinyl and Picoloyl Substituents on the Stereoselectivity of Chemical Glycosylation
inferredcites →https://doi.org/10.1021/ja803378kopenalex-snapshot
Palladium(II)-Catalyzed Rearrangement of Glycal Trichloroacetimidates: Application to the Stereoselective Synthesis of Glycosyl Ureas
inferredcites →https://doi.org/10.1021/ja9053948openalex-snapshot
Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of Enol Carbonates
inferredcites →https://doi.org/10.1021/ja9828713openalex-snapshot
Regio- and Enantioselective Allylic Alkylation of an Unsymmetrical Substrate: A Working Model
inferredcites →https://doi.org/10.1021/jo702436popenalex-snapshot
Cationic Palladium(II)-Catalyzed Stereoselective Glycosylation with Glycosyl Trichloroacetimidates
inferredcites →https://doi.org/10.1021/ol0342305openalex-snapshot
Oxazolidinone Protection of N-Acetylglucosamine Confers High Reactivity on the 4-Hydroxy Group in Glycosylation
inferredcites →https://doi.org/10.1021/ol071268zopenalex-snapshot
Palladium-Catalyzed Stereoselective Formation of α-O-Glycosides
inferredcites →https://doi.org/10.1021/ol201231vopenalex-snapshot
Glycoside Bond Formation via Acid–Base Catalysis
inferredcites →https://doi.org/10.1021/ol401095kopenalex-snapshot
Selective Synthesis of 1,2-cis-α-Glycosides without Directing Groups. Application to Iterative Oligosaccharide Synthesis
inferredcites →https://doi.org/10.1021/ol402503zopenalex-snapshot
Regio- and Stereoselective Direct N-Alkenylation of Indoles via Pd-Catalyzed Aerobic Oxidation
inferredcites →https://doi.org/10.1038/ncomms11806openalex-snapshot
Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism
inferredcites →https://doi.org/10.1039/c1cc16011gopenalex-snapshot
Decarboxylative benzylation and arylation of nitriles
inferredcites →https://doi.org/10.1080/07328303.2012.683910openalex-snapshot
Recent Advances in Transition Metal–CatalyzedO-Glycosylations
inferredcites →https://doi.org/10.1126/science.aal1875openalex-snapshot
Macrocyclic bis-thioureas catalyze stereospecific glycosylation reactions

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4659364openalex-extracted
inferred← citeshttps://doi.org/10.1002/0471264180.or100.13openalex-snapshot
Catalyst‐Controlled Glycosylation
inferred← citeshttps://doi.org/10.1002/adsc.202300211openalex-snapshot
One‐Pot Stereoselective Synthesis of 2,3,4‐Unprotected β‐N‐Glycopyranosides from Glycals and Amines
inferred← citeshttps://doi.org/10.1002/advs.202519766openalex-snapshot
Stereoselective Ferrier‐Type O ‐Glycosylation Enabled by Difluoromethylated Glycal Donors
inferred← citeshttps://doi.org/10.1002/ange.201812222openalex-snapshot
A Convergent Synthetic Strategy towards Oligosaccharides containing 2,3,6‐Trideoxypyranoglycosides
inferred← citeshttps://doi.org/10.1002/ange.202302569openalex-snapshot
Ligand‐Controlled Stereoselective Synthesis and Biological Activity of 2‐Exomethylene Pseudo‐glycoconjugates: Discovery of Mincle‐Selective Ligands
inferred← citeshttps://doi.org/10.1002/anie.201812222openalex-snapshot
A Convergent Synthetic Strategy towards Oligosaccharides containing 2,3,6‐Trideoxypyranoglycosides
inferred← citeshttps://doi.org/10.1002/anie.202302569openalex-snapshot
Ligand‐Controlled Stereoselective Synthesis and Biological Activity of 2‐Exomethylene Pseudo‐glycoconjugates: Discovery of Mincle‐Selective Ligands
inferred← citeshttps://doi.org/10.1002/asia.202101156openalex-snapshot
o‐Cyanobenzoate: A Recyclable and Reusable Stereo‐directing Group for β‐O‐Glycosylation via Pd(0)‐catalyzed Ferrier Rearrangement
inferred← citeshttps://doi.org/10.1002/asia.202301013openalex-snapshot
An Open‐Air Palladium‐Catalyzed Stereoselective O‐Glycosylation of Glycals via in‐situ Generation of gem‐Disubstituted Methanols from p‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/asia.70583openalex-snapshot
Recent Advances in Palladium‐Catalyzed Functionalization of Carbohydrate Frameworks
inferred← citeshttps://doi.org/10.1002/cjoc.70692openalex-snapshot
Stereodivergent Access to N‐ Glycosyl Sulfonamides via Palladium‐Catalyzed N ‐Glycosylation of Pyranone Donors
inferred← citeshttps://doi.org/10.1002/ejoc.202501095openalex-snapshot
Design, Stereoselective Synthesis, and in Silico Evaluation of Novel Pyran‐Based C ‐Fucosides as Potential COX‐2 Inhibitors
inferred← citeshttps://doi.org/10.1002/tcr.202400067openalex-snapshot
Stereoselective Synthesis of Glycosides via Tsuji–Trost Type Glycosylation Using 3,4‐Carbonate Galactals
inferred← citeshttps://doi.org/10.1016/j.carres.2018.10.006openalex-snapshot
Recent advances in reagent-controlled stereoselective/stereospecific glycosylation
inferred← citeshttps://doi.org/10.1016/j.carres.2025.109596openalex-snapshot
Stereoselective synthesis of 2,3-unsaturated O-aryl glycosides from glycals using Tris(pentafluorophenyl)borane as catalyst
inferred← citeshttps://doi.org/10.1016/j.checat.2022.10.019openalex-snapshot
Recent advances in transition-metal-catalyzed glycosyl cross-coupling reactions
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/10.1021/acs.accounts.7b00449openalex-snapshot
Venturing beyond Donor-Controlled Glycosylation: New Perspectives toward Anomeric Selectivity
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00975openalex-snapshot
Direct N-Glycosylation of Amides/Amines with Glycal Donors
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01170openalex-snapshot
Selective Synthesis of Some Aminosugars via Catalytic Aminohydroxylation of Protected 2,3-Unsaturated d -Gluco- and d -Galacto-2-hexenopyranosides
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02832openalex-snapshot
Synthesis of the Tetrasaccharide Glycone Part of Tetrocarcin A
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01011openalex-snapshot
Stereoselective Synthesis of O -Glycosides with Borate Acceptors
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00554openalex-snapshot
Reaction Rate and Stereoselectivity Enhancement in Glycosidations with O-Glycosyl Trihaloacetimidate Donors due to Catalysis by a Lewis Acid–Nitrile Cooperative Effect
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00698openalex-snapshot
Stereoselective Synthesis of β- S -Glycosides via Palladium Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01218openalex-snapshot
Convergent Palladium-Catalyzed Stereospecific Arginine Glycosylation Using Glycals
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01404openalex-snapshot
Convergent Synthesis of Tetrasaccharide Fragment of Cervimycin K
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02060openalex-snapshot
Synthetic Study toward Saccharomicin Based upon Asymmetric Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04378openalex-snapshot
Stereoselective O-Glycosylation of Glycals with Arylboronic Acids Using Air as the Oxygen Source
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02881openalex-snapshot
β-C-Glycosylation with 2-Oxindole Acceptors via Palladium-Catalyzed Decarboxylative Reactions
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c04379openalex-snapshot
Stereoselective Synthesis of 2-Deoxy Glycosides via Iron Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01484openalex-snapshot
Stereospecific Palladium-Catalyzed Direct Glycosylation of Oximes: Access to N–O-Linked Glycosides
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01541openalex-snapshot
Synthesis of Sterically Hindered Dialkyl Ethers via Palladium-Catalyzed Fluoro-alkoxylation of gem-Difluoroalkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02466openalex-snapshot
Palladium-Catalyzed Regio- and Stereoselective Glycosylation of Azole Heterocycles Enables Access to Diverse Heterocyclic N-Glycosides
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04771openalex-snapshot
Palladium-Catalyzed Stereospecific Glycosylation Enables Divergent Synthesis of N–O-Linked Glycosides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00895openalex-snapshot
One-Pot Stereoselective Synthesis of C -Glycosyl Amino Acids with Vicinal Stereocenters
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03416openalex-snapshot
Stereoselective Synthesis of N–O-Linked α- N -Acetylgalactosaminoglycosides via Oxime O -Glycosylation with 2-Nitrogalactals
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04215openalex-snapshot
Silicon-Assisted Ferrier Rearrangement in Preparation of C3-Silyl Glycosides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04954openalex-snapshot
Strong Base-Promoted Pd-Catalyzed Asymmetric Hydroalkoxylation of Alkoxyallene
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c05313openalex-snapshot
Regio- and Stereoselective Synthesis of 1-/3-Sulfone Sugars Controlled by the Amount of SnCl 4
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01506openalex-snapshot
General Strategy for Stereoselective Synthesis of β-N-Glycosyl Sulfonamides via Palladium-Catalyzed Glycosylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04665openalex-snapshot
Open-Air Stereoselective Construction of C -Aryl Glycosides
inferred← citeshttps://doi.org/10.1021/acscatal.0c00753openalex-snapshot
Superbase-Catalyzed Stereo- and Regioselective Glycosylation with 2-Nitroglycals: Facile Access to 2-Amino-2-deoxy-O-glycosides
inferred← citeshttps://doi.org/10.1021/acscatal.1c00225openalex-snapshot
Catalyst-Controlled Regiodivergent Synthesis of 1- and 3-Thiosugars with High Stereoselectivity and Chemoselectivity
inferred← citeshttps://doi.org/10.1021/acscatal.9b00336openalex-snapshot
Palladium-Catalyzed Stereospecific C -Glycosylation of Glycals with Vinylogous Acceptors
inferred← citeshttps://doi.org/10.1039/9781788016575-00015openalex-snapshot
Methodologies in Chemical Syntheses of Carbohydrates
inferred← citeshttps://doi.org/10.1039/c9cc07194fopenalex-snapshot
2- O -Benzyloxycarbonyl protected glycosyl donors: a revival of carbonate-mediated anchimeric assistance for diastereoselective glycosylation
inferred← citeshttps://doi.org/10.1039/d0sc06529copenalex-snapshot
Iridium-promoted deoxyglycoside synthesis: stereoselectivity and mechanistic insight
inferred← citeshttps://doi.org/10.1039/d2qo01308hopenalex-snapshot
Palladium catalyzed decarboxylative β- C -glycosylation of glycals with oxazol-5-(4 H )-ones as acceptors
inferred← citeshttps://doi.org/10.1039/d3cc04063aopenalex-snapshot
Facile and stereospecific synthesis of diverse β- N -glycosyl sulfonamide scaffolds via palladium catalysis
inferred← citeshttps://doi.org/10.1039/d4qo00410hopenalex-snapshot
Stereoselective strain-release Ferrier rearrangement: the dual role of catalysts
inferred← citeshttps://doi.org/10.1039/d4qo01619jopenalex-snapshot
Synthesis of C -glycosides enabled by palladium-catalyzed glycosylation reactions
inferred← citeshttps://doi.org/10.1055/a-2348-2803openalex-snapshot
Highly Regio-/Stereoselective Synthesis of Carbohydrates with Unsaturated Glycosyl Donors under Mild Conditions
inferred← citeshttps://doi.org/10.2139/ssrn.5180060openalex-snapshot
Stereoselective Synthesis of 2,3-Unsaturated O-Aryl Glycosides from Glycals Using Tris(Pentafluorophenyl)Borane as Catalyst
inferred← citeshttps://doi.org/10.2174/1385272824666200130111142openalex-snapshot
Progress in the Synthesis of 2,3-unsaturated Glycosides
inferred← citeshttps://doi.org/10.2174/9789815322798125010005openalex-snapshot
Recent Advances in the Synthesis of O- and S-Glycosides from Glycals
inferred← citeshttps://doi.org/10.3389/fmolb.2022.896187openalex-snapshot
Recent Advances in Stereoselective Chemical O-Glycosylation Reactions
inferred← citeshttps://doi.org/10.3390/molecules27217234openalex-snapshot
Acid Catalyzed Stereocontrolled Ferrier-Type Glycosylation Assisted by Perfluorinated Solvent
inferred← citeshttps://doi.org/10.3390/molecules27227979openalex-snapshot
Stereoselective Synthesis of 2-Deoxythiosugars from Glycals
inferred← citeshttps://doi.org/10.6023/cjoc202202002openalex-snapshot
Open-Air Stereoselective Synthesis of C-Aryl Fucosides/Arabinosides
inferred← citeshttps://doi.org/10.6023/cjoc202204050openalex-snapshot
Research Advances in Functional Group-Directed Stereoselective Glycosylation
inferred← citeshttps://doi.org/10.6023/cjoc202303019openalex-snapshot
Pd-Catalyzed Stereoselective Synthesis of Nitroalkyl β-C-Glycosides
inferred← citeshttps://doi.org/10.6023/cjoc202307001openalex-snapshot
Regio- and Stereo-selective Synthesis of 1β-/3R-Aryl Thiosugar
inferred← citeshttps://doi.org/10.6023/cjoc202502005openalex-snapshot
Progress in the Construction of Functionalized Derivatives Based on Dihydropyran Skeleton Modification
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