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Formation of β-Mannopyranosides of Primary Alcohols Using the Sulfoxide Method
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.198201553openalex-snapshot
Advances in Selective Chemical Syntheses of Complex Oligosaccharides
inferredcites →https://doi.org/10.1002/anie.198810861openalex-snapshot
β‐Mannosides from β‐Glucosides by Intramolecular Nucleophilic Substitution with Inversion of Configuration
inferredcites →https://doi.org/10.1002/anie.199008233openalex-snapshot
Syntheses, Conformations and X‐Ray Structure Analyses of the Saccharide Chains from the Core Regions of Glycoproteins
inferredcites →https://doi.org/10.1002/anie.199411021openalex-snapshot
Synthesis of a Biantennary Heptasaccharide by Regioselective Glycosylations
inferredcites →https://doi.org/10.1002/cber.19811140916openalex-snapshot
Bausteine von Oligosacchariden, XXX. Neue effektive β‐Glycosidsynthese für Mannose‐Glycoside Synthesen von Mannose‐haltigen Oligosacchariden
inferredcites →https://doi.org/10.1002/cber.19821150106openalex-snapshot
O‐Alkylierung am anomeren Zentrum, 4. 1‐O‐Alkylierung von D ‐Mannofuranose und D ‐Mannopyranose
inferredcites →https://doi.org/10.1016/0003-9861(90)90248-wopenalex-snapshot
Structural study of cell wall phosphomannan of Candida albicans NIH B-792 (serotype B) strain, with special reference to 1H and 13C NMR analyses of acid-labile oligomannosyl residues
inferredcites →https://doi.org/10.1016/0008-6215(89)80006-0openalex-snapshot
Structural analysis of phospho-d-mannan-protein complexes isolated from yeast and mold form cells of Candida albicans NIH A-207 serotype a strain
inferredcites →https://doi.org/10.1016/0008-6215(90)80154-uopenalex-snapshot
Identification of the lipopolysaccharide O-chain ofEscherichia hermannii (ATCC 33651) as ad-rhamnan
inferredcites →https://doi.org/10.1016/0040-4039(95)01604-xopenalex-snapshot
Stereocontrolled synthesis of the pentasaccharide core structure of asparagine-linked glycoprotein oligosaccharide based on a highly convergent strategy
inferredcites →https://doi.org/10.1016/s0008-6215(00)83543-0openalex-snapshot
The 13C-n.m.r. spectra of disaccharides of d-glucose, d-galactose, and l-rhamnose as models for immununological polysaccharides
inferredcites →https://doi.org/10.1016/s0021-9258(17)34824-xopenalex-snapshot
Soybean agglutinin–a plant glycoprotein. Structure of the carboxydrate unit.
inferredcites →https://doi.org/10.1016/s0021-9258(17)37814-6openalex-snapshot
Structural studies of the major high mannose oligosaccharide units from Chinese hamster ovary cell glycoproteins.
inferredcites →https://doi.org/10.1016/s0021-9258(18)43329-7openalex-snapshot
Primary structure of the carbohydrate chain of soybean agglutinin. A reinvestigation by high resolution 1H NMR spectroscopy.
inferredcites →https://doi.org/10.1016/s0021-9258(18)86956-3openalex-snapshot
Assignment of intrachain disulfide bonds and characterization of potential glycosylation sites of the type 1 recombinant human immunodeficiency virus envelope glycoprotein (gp120) expressed in Chinese hamster ovary cells.
inferredcites →https://doi.org/10.1016/s0021-9258(19)68543-1openalex-snapshot
Characterization of a novel glycosphingolipid, ceramide nonasaccharide, isolated from spermatozoa of the fresh water bivalve, Hyriopsis schlegelii.
inferredcites →https://doi.org/10.1016/s0040-4039(00)73450-2openalex-snapshot
Intramolecular hydrogen atom abstraction in carbohydrates and nucleosides: Inversion of an α- to β-mannopyranoside and generation of thymidine C-4′ radicals
inferredcites →https://doi.org/10.1016/s0040-4039(00)73451-4openalex-snapshot
Synthesis of β-mannopyranosides from α-epimers by radical inversion
inferredcites →https://doi.org/10.1016/s0040-4039(00)76728-1openalex-snapshot
Trimethylsilyl triflate mediated chemoselective condensation of arylsulfenyl glycosides
inferredcites →https://doi.org/10.1021/cr00020a006openalex-snapshot
Recent progress in O-glycosylation methods and its application to natural products synthesis
inferredcites →https://doi.org/10.1021/ja00024a057openalex-snapshot
Synthesis of .beta.-mannopyranosides by intramolecular aglycon delivery
inferredcites →https://doi.org/10.1021/ja00029a047openalex-snapshot
Stereocontrolled synthesis of disaccharides via the temporary silicon connection
inferredcites →https://doi.org/10.1021/ja00057a056openalex-snapshot
A one step synthesis of the ciclamycin trisaccharide
inferredcites →https://doi.org/10.1021/ja00070a048openalex-snapshot
A ready, convergent synthesis of the heptasaccharide GPI membrane anchor of rat brain Thy-1 glycoprotein
inferredcites →https://doi.org/10.1021/ja00084a018openalex-snapshot
Concise Synthesis of the Calicheamicin Oligosaccharide Using the Sulfoxide Glycosylation Method
inferredcites →https://doi.org/10.1021/ja00106a021openalex-snapshot
Regiospecific 4,6-Functionalization of Pyranosides via Dimethylboron Bromide-Mediated Cleavage of Phthalide Orthoesters
inferredcites →https://doi.org/10.1021/ja00199a081openalex-snapshot
Glycosylation of unreactive substrates
inferredcites →https://doi.org/10.1021/ja9532291openalex-snapshot
Stereoselective Synthesis of β-Mannopyranosides via the Temporary Silicon Connection Method
inferredcites →https://doi.org/10.1021/jm00160a025openalex-snapshot
Cardiac glycosides. 7. Sugar stereochemistry and cardiac glycoside activity
inferredcites →https://doi.org/10.1021/jo00101a035openalex-snapshot
3,4,6-Tri-O-benzyl-.alpha.-D-arabino-hexopyranos-2-ulosyl Bromide: A Versatile Glycosyl Donor for the Efficient Generation of .beta.-D-Mannopyranosidic Linkages
inferredcites →https://doi.org/10.1021/jo00101a036openalex-snapshot
Practical Synthesis of .beta.-D-Xyl-(1.fwdarw.2)-.beta.-D-Man-(1.fwdarw.4)-.alpha.-D-Glc-OMe, a Trisaccharide Component of the Hyriopsis schlegelii Glycosphingolipid
inferredcites →https://doi.org/10.1021/jo00120a002openalex-snapshot
A Convergent and Stereocontrolled Synthetic Route to the Core Pentasaccharide Structure of Asparagine-Linked Glycoproteins
inferredcites →https://doi.org/10.1021/jo951194hopenalex-snapshot
Chemistry of 1-Alkoxy-1-glycosyl Radicals: The Manno- and Rhamnopyranosyl Series. Inversion of α- to β-Pyranosides and the Fragmentation of Anomeric Radicals
inferredcites →https://doi.org/10.1055/s-1992-21485openalex-snapshot
Improved Synthesis of β-Mannopyranosides by Intramolecular Aglycon Delivery
inferredcites →https://doi.org/10.1055/s-1995-5291openalex-snapshot
p-Methoxybenzyl Ethers as Acid-Labile Protecting Groups in Oligosaccharide Synthesis
inferredcites →https://doi.org/10.1097/00002030-198912000-00003openalex-snapshot
Oligosaccharide-mediated interactions of the envelope glycoprotein gp120 of HIV-1 that are independent of CD4 recognition
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/10.1246/bcsj.67.1359openalex-snapshot
New Synthetic Methods and Reagents for Complex Carbohydrates. VIII. Stereoselective α- and β-Mannopyranoside Formation from Glycosyl Dimethylphosphinothioates with the C-2 Axial Benzyloxyl Group
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Synthesis of Glycosides
inferred← citeshttps://doi.org/10.1016/b978-012312085-4/50006-4openalex-snapshot
Synthesis and Activation of Carbohydrate Donors: Thioglycosides and Sulfoxides
inferred← citeshttps://doi.org/10.1016/b978-012312085-4/50010-6openalex-snapshot
The Stereoselective Synthesis of β-Mannosides
inferred← citeshttps://doi.org/10.1016/b978-044451967-2/00008-8openalex-snapshot
O-Glycosidation Methods
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.bmc.2010.04.013openalex-snapshot
Effects of frozen conditions on stereoselectivity and velocity of O-glycosylation reactions
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.12.052openalex-snapshot
Structure–activity relationship studies on acremomannolipin A, the potent calcium signal modulator with a novel glycolipid structure 2: Role of the alditol side chain stereochemistry
inferred← citeshttps://doi.org/10.1016/j.bmc.2015.03.079openalex-snapshot
Structure–activity relationship studies on acremomannolipin A, the potent calcium signal modulator with a novel glycolipid structure 3: Role of the length of alditol side chain
inferred← citeshttps://doi.org/10.1016/j.carres.2003.10.029openalex-snapshot
A convergent strategy for the preparation of N-glycan core di-, tri-, and pentasaccharide thioaldoses for the site-specific glycosylation of peptides and proteins bearing free cysteines
inferred← citeshttps://doi.org/10.1016/j.carres.2004.11.025openalex-snapshot
Environmentally benign β-stereoselective glycosidations of glycosyl phosphites using a reusable heterogeneous solid acid, montmorillonite K-10
inferred← citeshttps://doi.org/10.1016/j.carres.2006.03.012openalex-snapshot
Novel glycosylation methods and their application to natural products synthesis
inferred← citeshttps://doi.org/10.1016/j.carres.2006.09.002openalex-snapshot
The use of cyclic bifunctional protecting groups in oligosaccharide synthesis—an overview
inferred← citeshttps://doi.org/10.1016/j.carres.2007.11.018openalex-snapshot
Synthesis of trans-fused tetrahydrooxepins: stereoselective allylation of sulfur or fluoro-substituted tetrahydrooxepins
inferred← citeshttps://doi.org/10.1016/j.carres.2010.05.031openalex-snapshot
A highly α-selective glycosylation for the convenient synthesis of repeating α-(1→4)-linked N-acetyl-galactosamine units
inferred← citeshttps://doi.org/10.1016/j.carres.2010.06.004openalex-snapshot
Computational study of the influence of cyclic protecting groups in stereoselectivity of glycosylation reactions
inferred← citeshttps://doi.org/10.1016/j.carres.2012.05.025openalex-snapshot
Influence of protecting groups on the anomeric equilibrium; case of the 4,6-O-benzylidene acetal in the mannopyranose series
inferred← citeshttps://doi.org/10.1016/j.carres.2013.11.016openalex-snapshot
Is an acyl group at O-3 in glucosyl donors able to control α-stereoselectivity of glycosylation? The role of conformational mobility and the protecting group at O-6
inferred← citeshttps://doi.org/10.1016/j.carres.2014.07.004openalex-snapshot
Additive-controlled stereoselective glycosylations of 2,3-oxazolidinone protected glucosamine or galactosamine thioglycoside donors with phenols based on preactivation protocol
inferred← citeshttps://doi.org/10.1016/j.carres.2019.01.013openalex-snapshot
Stereoselective trimethylsilylation of α- and β-galactopyranoses
inferred← citeshttps://doi.org/10.1016/j.carres.2021.108421openalex-snapshot
2,3-Carbamate mannosamine glycosyl donors in glycosylation reactions of diacetone-d-glucose. An experimental and theoretical study
inferred← citeshttps://doi.org/10.1016/j.carres.2025.109396openalex-snapshot
Named reaction in carbohydrate chemistry: A review
inferred← citeshttps://doi.org/10.1016/j.cclet.2017.09.044openalex-snapshot
Approaches towards the core pentasaccharide in N- linked glycans
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.02.071openalex-snapshot
Catalytic and highly stereoselective β-mannopyranosylation using a 2,6-lactone-bridged mannopyranosyl ortho-hexynylbenzoate as donor
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.112235openalex-snapshot
Chemical strategies for the stereoselective construction of 1,2-cis-galacturonic and aminogalacturonic acid glycosides
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.05.034openalex-snapshot
Structure–activity relationship studies on acremomannolipin A, the potent calcium signal modulator with a novel glycolipid structure 4: Role of acyl side chains on d-mannose
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/10.1016/j.tet.2004.04.071openalex-snapshot
Stereocontrolled glycosidations using a heterogeneous solid acid, sulfated zirconia, for the direct syntheses of α- and β-manno- and 2-deoxyglucopyranosides
inferred← citeshttps://doi.org/10.1016/j.tet.2004.08.076openalex-snapshot
A highly stereoselective construction of 1,2-trans-β-glycosidic linkages capitalizing on 2-azido-2-deoxy-d-glycosyl diphenyl phosphates as glycosyl donors
inferred← citeshttps://doi.org/10.1016/j.tet.2005.01.070openalex-snapshot
Use of O-glycosylation in total synthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2005.08.090openalex-snapshot
Direct and stereoselective synthesis of β-d-mannosides using 4,6-O-benzylidene-protected mannosyl diethyl phosphite as a donor
inferred← citeshttps://doi.org/10.1016/j.tet.2008.05.051openalex-snapshot
Glycosulfoxides in carbohydrate chemistry
inferred← citeshttps://doi.org/10.1016/j.tet.2012.09.037openalex-snapshot
Syntheses of novel acarviosin analogs with anhydro or unsaturated sugar moieties
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.086openalex-snapshot
Stereoselective total synthesis of acremomannolipin A and its anomer, the potent calcium signal modulators with a novel glycolipid structure: role of the stereochemistry at the anomeric center on the activity
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.02.024openalex-snapshot
A unique approach to the synthesis of a dengue vaccine and the novel tetrasaccharide that results
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.07.128openalex-snapshot
A novel glycosidation of glycosyl fluoride using a designed ionic liquid and its effect on the stereoselectivity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.064openalex-snapshot
Direct glycosylation with anomeric hydroxy sugars by activation with 3-fluorophthalic anhydride and trifluoromethanesulfonic anhydride
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.04.060openalex-snapshot
A convenient synthesis of the core trisaccharide of the N-glycans
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.128openalex-snapshot
The first total synthesis of acremomannolipin A, the potential Ca2+ signal modulator with a characteristic glycolipid structure, isolated from the filamentous fungus Acremonium strictum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.066openalex-snapshot
2-Pyridyl glycoside: an alternative glycosyl donor in preactivation protocol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.045openalex-snapshot
A convenient preparation of glycosyl sulfoxides and its application to the synthesis of Salidroside epimer
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.04.049openalex-snapshot
Stereoselective β-mannosylation via anomeric O-alkylation: Formal synthesis of potent calcium signal modulator acremomannolipin A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.12.077openalex-snapshot
Recent topics in β-stereoselective mannosylation
inferred← citeshttps://doi.org/10.1016/s0008-6215(03)00234-9openalex-snapshot
Environmentally benign and stereoselective formation of β-mannosidic linkages utilizing 2,3-di-O-benzyl-4,6-O-benzylidene-protected mannopyranosyl phosphite and montmorillonite K-10
inferred← citeshttps://doi.org/10.1016/s0008-6215(97)00261-9openalex-snapshot
The chemoenzymatic synthesis of the core trisaccharide of N-linked oligosaccharides using a recombinant β-mannosyltransferase
inferred← citeshttps://doi.org/10.1016/s0008-6215(97)10040-4openalex-snapshot
Enzymatic synthesis of disaccharides using Agrobacterium sp. β-glucosidase
inferred← citeshttps://doi.org/10.1016/s0008-6215(99)00116-0openalex-snapshot
Chemoenzymatic synthesis of the Salmonella group E1 core trisaccharide using a recombinant β-(1→4)-mannosyltransferase
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)00093-4openalex-snapshot
Chemical Transformations Induced by Triflic Anhydride
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00760-8openalex-snapshot
Synthesis of disaccharides containing α-linked GlcNAc or β-linked ManNAc units
inferred← citeshttps://doi.org/10.1016/s0040-4020(96)00950-7openalex-snapshot
Synthesis of 2-hydroxy-6-{[(16R)-β-δ-mannopyransyloxy]heptadecyl}benzoic acid, a fungal metabolite with GABAA ion channel receptor inhibiting properties
inferred← citeshttps://doi.org/10.1016/s0040-4020(98)00426-8openalex-snapshot
Direct chemical synthesis of β-mannopyranosides and other glycosides via glycosyl triflates
inferred← citeshttps://doi.org/10.1016/s0040-4020(98)01202-2openalex-snapshot
Direct synthesis of β-mannosides. Synthesis of β-D-xyl-(1→2)-β-D-man-(1→4)-α-D-Glc-OMe: A trisaccharide component of the Hyriopsis schlegelii glycosphingolipid. Formation of an orthoester from a xylopyranosyl sulfoxide
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)01053-4openalex-snapshot
Synthesis of 4- O - d -Mannopyranosyl-α- d -glucopyranosides by Intramolecular Glycosylation of 6- O -Tethered Mannosyl Donors
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)00887-xopenalex-snapshot
Sulfur atom configuration of sulfinyl galactofuranosides determines different reactivities in glycosylation reactions
inferred← citeshttps://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?
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00674-8openalex-snapshot
Novel stereocontrolled α- and β-glycosidations of mannopyranosyl sulfoxides using environmentally benign heterogeneous solid acids
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)00965-4openalex-snapshot
Synthesis OF differentially protected phenyl d-thioglucopyranosides and 1-phenyl d-thioglucopyranosiduronic acids
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(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/s0957-4166(01)00437-2openalex-snapshot
Unexpected fluorous solvent effect on oxidation of 1-thioglycosides
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/10.1021/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.8b00066openalex-snapshot
Toward Automated Enzymatic Synthesis of Oligosaccharides
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.chemrev.8b00144openalex-snapshot
Catalytic Glycosylations in Oligosaccharide Synthesis
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.0c02370openalex-snapshot
Stereoselective Synthesis of 2-Azido-2-deoxy-β- d -mannosides via Cs2CO3-Mediated Anomeric O-Alkylation with Primary Triflates: Synthesis of a Tetrasaccharide Fragment of Micrococcus luteus Teichuronic Acid
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01009openalex-snapshot
Reinvestigation of N,N-Diacetylimido-Protected 2-Aminothioglycosides in O-Glycosylation: Intermolecular Hydrogen Bonds Contributing to 1,2-Orthoamide Formation
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.2c01475openalex-snapshot
α-Selective Glucosylation Can Be Achieved with 6-O-para-Nitrobenzoyl Protection
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02397openalex-snapshot
Exploring the Dual Functions of Distal Acyl Group Direction in Various Nucleophilic Environments
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02956openalex-snapshot
The Stereochemical Outcome of Galactosylations Is Influenced by Both the Position and Electron-Withdrawing Power of Distal Acyl Protecting Groups
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.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.7b00057openalex-snapshot
Synthesis of β-(1→2)-Linked 6-Deoxy- l -altropyranose Oligosaccharides via Gold(I)-Catalyzed Glycosylation of an ortho-Hexynylbenzoate Donor
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00470openalex-snapshot
Stereoselectivity of Conformationally Restricted Glucosazide Donors
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02394openalex-snapshot
Total Synthesis of the Trisaccharide Antigen of the Campylobacter jejuni RM1221 Capsular Polysaccharide via de Novo Synthesis of the 6-Deoxy- d -manno-heptose Building Blocks
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03056openalex-snapshot
Manual and Automated Syntheses of the N-Linked Glycoprotein Core Glycans
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00732openalex-snapshot
Stereoselective Phenylselenoglycosylation of Glycals Bearing a Fused Carbonate Moiety toward the Synthesis of 2-Deoxy-β-galactosides and β-Mannosides
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00969openalex-snapshot
Promoter-Assisted Stereoselective Synthesis of the 6-Deoxy-β- d -manno-heptopyranose Oligosaccharides
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02566openalex-snapshot
β- l -Rhamnosylation and β- d -Mannosylation Mediated by 4- O -Ester Groups in a Weakly Nucleophilic Environment
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04208openalex-snapshot
[Au]/[Ag]-Catalyzed Glycosidation of Ethynylcyclohexyl Glycosyl Carbonates Enables Direct Stereoselective Synthesis of 2-Azido-2-deoxy-β-mannopyranosides
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04838openalex-snapshot
2,2-Dichloro-1,3-benzodioxole as a Hydroxyl Protection Reagent for Carbohydrate Compounds
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02226openalex-snapshot
Achiral 2-Hydroxy Protecting Group for the Stereocontrolled Synthesis of 1,2-cis-α-Glycosides by Six-Ring Neighboring Group Participation
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/acs.orglett.8b01979openalex-snapshot
Stereodivergent Mannosylation Using 2-O-(ortho-Tosylamido)benzyl Group
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02669openalex-snapshot
Total Synthesis of Trisaccharide Repeating Unit of O-Specific Polysaccharide of Pseudomonas fluorescens BIM B-582
inferred← citeshttps://doi.org/10.1021/acscatal.0c05378openalex-snapshot
Facile Enzymatic Synthesis of Diverse Naturally-Occurring β- d -Mannopyranosides Catalyzed by Glycoside Phosphorylases
inferred← citeshttps://doi.org/10.1021/ar100035ropenalex-snapshot
Mechanism of a Chemical Glycosylation Reaction
inferred← citeshttps://doi.org/10.1021/ar5004362openalex-snapshot
The Logic of Automated Glycan Assembly
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
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