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Stereoselective Synthesis of α- and β-Glycosylamide Derivatives from Glycopyranosyl Azides via Isoxazoline Intermediates
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0008-6215(90)80006-oopenalex-snapshot
Synthesis of the α and β anomer of an N-triglycosyl dipeptide
inferredcites →https://doi.org/10.1016/0008-6215(93)84082-hopenalex-snapshot
Syntheses of nephritogenoside and related compounds
inferredcites →https://doi.org/10.1016/s0008-6215(99)00284-0openalex-snapshot
Syntheses of amphiphilic glycosylamides from glycosyl azides without transient reduction to glycosylamines
inferredcites →https://doi.org/10.1016/s0040-4020(01)00380-5openalex-snapshot
An easy access to anomeric glycosyl amides and imines(Schiff bases) via transformation of glycopyranosyl trimethylphosphinimides
inferredcites →https://doi.org/10.1016/s0040-4039(00)74132-3openalex-snapshot
Total synthesis of nephritogenic glycopeptide, nephritogenoside
inferredcites →https://doi.org/10.1021/cr990308copenalex-snapshot
Synthesis of Glycopeptides Containing Carbohydrate and Peptide Recognition Motifs
inferredcites →https://doi.org/10.1021/ja00170a055openalex-snapshot
n-Pentenyl glycosides as efficient synthons for promoter-mediated assembly of n-.alpha.-linked glycoproteins
inferredcites →https://doi.org/10.1021/ja00170a056openalex-snapshot
Facile aerial oxidation of the DNA-base adduct N-(2'-deoxyguanosin-8-yl)-2-aminofluorene [dG(C8)AF]
inferredcites →https://doi.org/10.1023/a:1011006122704openalex-snapshot
A journey to the world of glycobiology
inferredcites →https://doi.org/10.1073/pnas.80.18.5470openalex-snapshot
Asparaginylglucose: Novel type of carbohydrate linkage
inferredcites →https://doi.org/10.1073/pnas.91.15.7114openalex-snapshot
Glycopeptide enkephalin analogues produce analgesia in mice: evidence for penetration of the blood-brain barrier.
inferredcites →https://doi.org/10.1093/glycob/3.2.97openalex-snapshot
Biological roles of oligosaccharides: all of the theories are correct
inferredcites →https://doi.org/10.1515/znc-1999-9-1013openalex-snapshot
α-Tocopherol Protection Against Drought-Induced Damage In Rosmarinus Officinalis L. And Melissa Officinalis L.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Stereoselective Synthesis of α- and β-Glycosylamide Derivatives from Glycopyranosyl Azides via Isoxazoline Intermediates.
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inferred← citeshttps://doi.org/10.1002/ejoc.201100124openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201600350openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201801693openalex-snapshot
Catalytic Enantioselective Synthesis of 3,4,5‐Trisubstituted Isoxazoline N‐Oxides and Regioselective Synthesis of 3,4,5‐Trisubstituted Isoxazoles
inferred← citeshttps://doi.org/10.1002/ejoc.202000155openalex-snapshot
Interfering with the Sugar Code: Ten Years Later
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inferred← citeshttps://doi.org/10.1002/jhet.1000openalex-snapshot
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Mechanism and Regioselectivity of 1,3‐Dipolar Cycloaddition of Nitrile Oxides to 3‐Methylene Oxindole: A Density Functional Theory Study
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α-Glucopyranoimidazolines as intermediate analogue inhibitors of family 20 β-N-acetylglucosaminidases
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inferred← citeshttps://doi.org/10.1016/j.carres.2006.02.001openalex-snapshot
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Stereoselective synthesis of glycosyl amides by traceless Staudinger ligation of unprotected glycosyl azides
inferred← citeshttps://doi.org/10.1016/j.carres.2010.03.012openalex-snapshot
Monovalent and bivalent N-fucosyl amides as high affinity ligands for Pseudomonas aeruginosa PA-IIL lectin
inferred← citeshttps://doi.org/10.1016/j.carres.2015.08.002openalex-snapshot
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Substitution of dichloromethane with greener solvents for the preparation of thioglycosides and glycosyl azides, and for a glycosylation reaction. Deacetylation in ethanol-ethyl acetate
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An attractive route to transamidation catalysis: Facile synthesis of new o-aryloxide-N-heterocyclic carbene ruthenium(II) complexes containing trans triphenylphosphine donors
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IMesCuCl/TBHP system for aqueous oxidative amidation: Synthesis of new amide derivatives as EGFR targeting anti-breast cancer agents and computational studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138200openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2015.11.063openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.12.159openalex-snapshot
Selective synthesis of anomeric α-glycosyl acetamides via intramolecular Staudinger ligation of the α-azides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.05.066openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.048openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.018openalex-snapshot
nBu4NI-catalyzed oxidative amidation of aldehydes with tertiary amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.07.083openalex-snapshot
Oxidative synthesis of benzamides from toluenes and DMF
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.113openalex-snapshot
Copper-catalyzed oxidative amidation between aldehydes and arylamines under mild conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.08.066openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0065-2318(06)60004-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c01373openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.5b02385openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03334openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsanm.2c00859openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsomega.5c04718openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsomega.8b00732openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cc100122nopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/co5001844openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr5006974openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja0294919openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja049293copenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja056399eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja064315bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo0354948openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo060409sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo061703nopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo062419zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo200284aopenalex-snapshot
Iron(II)-Catalyzed Amidation of Aldehydes with Iminoiodinanes at Room Temperature and under Microwave-Assisted Conditions
inferred← citeshttps://doi.org/10.1021/jo400797topenalex-snapshot
HMDO-Promoted Peptide and Protein Synthesis in Ionic Liquids
inferred← citeshttps://doi.org/10.1021/jo500292mopenalex-snapshot
Ethyl 2-Cyano-2-(2-nitrobenzenesulfonyloxyimino)acetate (o-NosylOXY): A Recyclable Coupling Reagent for Racemization-Free Synthesis of Peptide, Amide, Hydroxamate, and Ester
inferred← citeshttps://doi.org/10.1021/la062678jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol048271sopenalex-snapshot
Stereoselective N-Glycosylation by Staudinger Ligation
inferred← citeshttps://doi.org/10.1021/ol102181ropenalex-snapshot
Catalytic Asymmetric Formal [4 + 1] Annulation Leading to Optically Active cis -Isoxazoline N -Oxides
inferred← citeshttps://doi.org/10.1021/ol203211kopenalex-snapshot
Peroxide-Mediated Transition-Metal-Free Direct Amidation of Alcohols with Nitroarenes
inferred← citeshttps://doi.org/10.1021/ol3012315openalex-snapshot
Diacetoxyiodobenzene Mediated One-Pot Synthesis of Diverse Carboxamides from Aldehydes
inferred← citeshttps://doi.org/10.1021/ol302175vopenalex-snapshot
One-Pot Synthesis of Amides from Aldehydes and Amines via C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/ol302961sopenalex-snapshot
Rapid Formation of N-Glycopeptides via Cu(II)-Promoted Glycosylative Ligation
inferred← citeshttps://doi.org/10.1021/ol701778zopenalex-snapshot
Palladium-Catalyzed Glycal Imidate Rearrangement: Formation of α- and β-N-Glycosyl Trichloroacetamides
inferred← citeshttps://doi.org/10.1021/ol901125nopenalex-snapshot
Generalized Anomeric Effect in gem-Diamines: Stereoselective Synthesis of α-N-Linked Disaccharide Mimics
inferred← citeshttps://doi.org/10.1039/b700157fopenalex-snapshot
Cyclic, modified and conjugated peptides
inferred← citeshttps://doi.org/10.1039/b716468hopenalex-snapshot
Highly enantioselective synthesis of isoxazoline N-oxides
inferred← citeshttps://doi.org/10.1039/c0ob00342eopenalex-snapshot
Oxidative amide synthesis directly from alcohols with amines
inferred← citeshttps://doi.org/10.1039/c1cc12327kopenalex-snapshot
Facile synthesis of carbohydrate-integrated isoxazolines through tandem [4+1] cycloaddition and rearrangement of 2-nitroglycals
inferred← citeshttps://doi.org/10.1039/c1gc15401jopenalex-snapshot
Metal-free direct amidation of peptidyl thiol esters with α-amino acid esters
inferred← citeshttps://doi.org/10.1039/c2jm34652dopenalex-snapshot
MnO2/graphene oxide: a highly active catalyst for amide synthesis from alcohols and ammonia in aqueous media
inferred← citeshttps://doi.org/10.1039/c2ob25793aopenalex-snapshot
Stereoselective synthesis of protected 3-amino-3,6-dideoxyaminosugars
inferred← citeshttps://doi.org/10.1039/c2ob26165kopenalex-snapshot
Asymmetric catalytic [4 + 1] annulations catalyzed by quinidine: enantioselective synthesis of multi-functionalized isoxazoline N-oxides
inferred← citeshttps://doi.org/10.1039/c3ob40170gopenalex-snapshot
Iron-catalysed oxidative amidation of alcohols with amines
inferred← citeshttps://doi.org/10.1039/c3ob41218kopenalex-snapshot
DDQ-promoted direct transformation of benzyl hydrocarbons to amides via tandem reaction of the CDC reaction and Beckmann rearrangement
inferred← citeshttps://doi.org/10.1039/c3ob41392fopenalex-snapshot
The direct amidation of α-diketones with amines via TBHP-promoted oxidative cleavage of C(sp2)–C(sp2) bonds
inferred← citeshttps://doi.org/10.1039/c4cc00621fopenalex-snapshot
Oxidative coupling of methylamine with an aminyl radical: direct amidation catalyzed by I 2 /TBHP with HCl
inferred← citeshttps://doi.org/10.1039/c4ra07658copenalex-snapshot
Synthesis of amides through an oxidative amidation of tetrazoles with aldehydes under transition-metal-free conditions
inferred← citeshttps://doi.org/10.1039/c4ra14856hopenalex-snapshot
Imidazolium salt-supported Mukaiyama reagent: an efficient condensation reagent for amide bond formation
inferred← citeshttps://doi.org/10.1039/c4sc00697fopenalex-snapshot
Selective radical amination of aldehydic C(sp 2 )–H bonds with fluoroaryl azides via Co( ii )-based metalloradical catalysis: synthesis of N-fluoroaryl amides from aldehydes under neutral and nonoxidative conditions
inferred← citeshttps://doi.org/10.1039/c5ob02376aopenalex-snapshot
Direct oxidative amidation of aldehydes with amines catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions via a dual-catalysis process
inferred← citeshttps://doi.org/10.1039/c5qo00125kopenalex-snapshot
Metal free access to amide compounds via peroxide-mediated NN double bond cleavage of azobenzenes
inferred← citeshttps://doi.org/10.1039/c5ra27826kopenalex-snapshot
Palladium nanoparticles immobilized on an amine-functionalized MIL-101(Cr) as a highly active catalyst for oxidative amination of aldehydes
inferred← citeshttps://doi.org/10.1039/c6ra20902eopenalex-snapshot
Green synthesis of primary, secondary, and tertiary amides through oxidative amidation of methyl groups with amine hydrochlorides over recyclable CoFe 2 O 4 NPs
inferred← citeshttps://doi.org/10.1039/c7nj01965copenalex-snapshot
An efficient catalyst-free one-pot synthesis of primary amides from the aldehydes of the Baylis–Hillman reaction
inferred← citeshttps://doi.org/10.1039/c7nj02257copenalex-snapshot
Copper-amino group complexes supported on silica-coated magnetite nanoparticles: efficient catalyst for oxidative amidation of methyl arenes
inferred← citeshttps://doi.org/10.1039/c7ra02942jopenalex-snapshot
Copper-catalyzed one-pot oxidative amidation between methylarenes and amines
inferred← citeshttps://doi.org/10.1039/c8gc00630jopenalex-snapshot
Iron( iii )-catalyzed selective N–O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N -vinyl-α,β-unsaturated ketonitrones
inferred← citeshttps://doi.org/10.1039/c9dt03440dopenalex-snapshot
CuI incorporated cobalt ferrite nanoparticles as a magnetically separable catalyst for oxidative amidation reaction
inferred← citeshttps://doi.org/10.1039/c9ra04216dopenalex-snapshot
One-pot synthesis of amides via the oxidative amidation of aldehydes and amines catalyzed by a copper-MOF
inferred← citeshttps://doi.org/10.1039/d0ob01601bopenalex-snapshot
Copper-catalyzed aerobic oxidative C–C bond cleavage of simple ketones for the synthesis of amides
inferred← citeshttps://doi.org/10.1039/d0ob02477eopenalex-snapshot
One step stereoselective synthesis of oxazoline-fused saccharides and their conversion into the corresponding 1,2- cis glycosylamines bearing various protected groups
inferred← citeshttps://doi.org/10.1039/d1nj00591jopenalex-snapshot
N -Heterocyclic carbene (NHC) catalyzed amidation of aldehydes with amines via the tandem N -hydroxysuccinimide ester formation
inferred← citeshttps://doi.org/10.1039/d3gc02526hopenalex-snapshot
Organophotocatalytic dehydrogenative preparation of amides directly from alcohols
inferred← citeshttps://doi.org/10.1039/d3ra07763bopenalex-snapshot
Synthesis of N -glycosyl amides: conformational analysis and evaluation as inhibitors of β-galactosidase from E. coli
inferred← citeshttps://doi.org/10.1055/s-0039-1690815openalex-snapshot
Reactions Catalyzed by 2-Halogenated Azolium Salts: From Halogen-Bond Donors to Brønsted-Acidic Salts
inferred← citeshttps://doi.org/10.1055/sos-sd-130-00001openalex-snapshot
30.1.3 Carbohydrate Derivatives (Including Nucleosides)
inferred← citeshttps://doi.org/10.1080/00304940509354969openalex-snapshot
SYNTHETIC GLYCODIVERSIFICATION. FROM AMINOSUGARS TO AMINOGLYCOSIDE ANTIBIOTICS. A REVIEW
inferred← citeshttps://doi.org/10.1080/00304948.2025.2550320openalex-snapshot
A Convenient Conversion of Pyrazole-4-carbaldehydes to Pyrazole-4-carboxamides
inferred← citeshttps://doi.org/10.1080/00397910600943709openalex-snapshot
Efficient Approach for the Synthesis of Novel Functionalized Isoxazolines from Limonene
inferred← citeshttps://doi.org/10.1134/s1068162021020278openalex-snapshot
Synthesis of New Substituted Diamides. Investigation of Their Antioxidant and Antibacterial Properties
inferred← citeshttps://doi.org/10.1155/2009/982658openalex-snapshot
Covalent Attachment of Carbohydrate Derivatives to an Evanescent Wave Fiber Bragg Grating Biosensor
inferred← citeshttps://doi.org/10.1248/cpb.c18-00255openalex-snapshot
Organocatalytic Direct α-Selective N-Glycosylation of Amide with Glycosyl Trichloroacetimidate
inferred← citeshttps://doi.org/10.1248/yakushi.126.1319openalex-snapshot
Development of Efficient Methods for Synthesis of Nitrogen-containing Compounds Using Carbamates, Acylhydrazines, and Ammonia
inferred← citeshttps://doi.org/10.14302/issn.2377-2549.jndc-23-4740openalex-snapshot
Stereoselective Synthesis of N-Glycosyl Oxazolines and Evaluation of Their Antiproliferative Activity
inferred← citeshttps://doi.org/10.18596/jotcsa.338218openalex-snapshot
Synthesis of New N-Phthalimide Substituted Tricyclic Imide Containing Isoxazoline and Bispiro Functional Group as Possible Anti-cancer Agents
inferred← citeshttps://doi.org/10.18596/jotcsa.627805openalex-snapshot
Synthesis of trans-diamide derivatives from fumaryl chloride and determination of DPPH scavenging activity of synthesized molecules
inferred← citeshttps://doi.org/10.3762/bjoc.11.249openalex-snapshot
Synthesis of D-fructose-derived spirocyclic 2-substituted-2-oxazoline ribosides
inferred← citeshttps://doi.org/10.7282/t3b27vndopenalex-snapshot
Novel peptidylaminoarylmethyl phosphoramide mustards for activation by prostate-specific antigen
inferred← citeshttps://doi.org/10.7282/t3wh2pxgopenalex-snapshot
Synthesis and evaluation of phosphoramide mustard prodrugs for site-specific activation
inferred← citeshttps://doi.org/10.7598/cst2014.727openalex-snapshot
Development of New Methodology for the Synthesis of Substituted Aromatic Amides
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