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Traceless Staudinger Ligation of Glycosyl Azides with Triaryl Phosphines: Stereoselective Synthesis of Glycosyl Amides
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Neo-glycoconjugates: stereoselective synthesis of α-glycosyl amides via Staudinger ligation reactions
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Unprotected sugar phosphinimines: A facile route to cyclic carbamates of amino sugars
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Syntheses of amphiphilic glycosylamides from glycosyl azides without transient reduction to glycosylamines
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An easy access to anomeric glycosyl amides and imines(Schiff bases) via transformation of glycopyranosyl trimethylphosphinimides
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Synthesis of Glycopeptides Containing Carbohydrate and Peptide Recognition Motifs
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Stabilization of RN:NN:PR3. Preparation and structural characterization of stable tetraarylphosphazide complexes containing molybdenum and tungsten
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Reactions of ethylenediamine-N,N'-diacetatodiaquo complexes of cobalt(III). 3. A kinetic study of the .beta.-cis-Co(EDDA)(OH2)2+ .dblharw. .alpha.-cis-Co(EDDA)(OH2)2+ isomerization reaction
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Stereoselective Synthesis of α- and β-Glycosylamide Derivatives from Glycopyranosyl Azides via Isoxazoline Intermediates
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The Reaction of Thio Acids with Azides: A New Mechanism and New Synthetic Applications
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Effects of Glycosylation on Peptide Conformation: A Synergistic Experimental and Computational Study
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Synthesis of C-Terminal Glycopeptides from Resin-Bound Glycosyl Azides via a Modified Staudinger Reaction
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Selective Reduction of Anomeric Azides to Amines with Tetrathiomolybdate: Synthesis of β- d -Glycosylamines
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On the Preparation of Carbohydrate−Protein Conjugates Using the Traceless Staudinger Ligation
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A “Traceless” Staudinger Ligation for the Chemoselective Synthesis of Amide Bonds
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Synthesis, Structure and Reactions of Glycosyl Azides
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Reaction of 3-azidopropanol with tris(dimethylamido)phosphorus and structure of the phosphazide reaction product
inferredcites →https://doi.org/10.1126/science.287.5460.2007openalex-snapshot
Cell Surface Engineering by a Modified Staudinger Reaction
inferredcites →https://doi.org/10.1126/science.287.5460.2010openalex-snapshot
A Fossil Snake with Limbs
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inferred← citeshttps://doi.org/10.21205/deufmd.2019216228openalex-snapshot
β-L-Arabinokloraloz’un Mono- ve Di-Sülfonat Esterleri; 3-O-Korunmuş-5-Azido ve 5-O-Alkil Türevleri
inferred← citeshttps://doi.org/10.2174/0113852728283109240216051223openalex-snapshot
Synthesis of Novel Propynyl Monoterpene Analogues and their Conjugates with β-DGlucopyranosides
inferred← citeshttps://doi.org/10.3390/molecules18088779openalex-snapshot
A Facile Synthesis of α-N-Ribosyl-Asparagine and α-N-Ribosyl-Glutamine Building Blocks
inferred← citeshttps://doi.org/10.3762/bjoc.14.56openalex-snapshot
AuBr3-catalyzed azidation of per-O-acetylated and per-O-benzoylated sugars
inferred← citeshttps://doi.org/10.5582/ddt.2012.v6.1.9openalex-snapshot
Synthesis of solasodine glycoside derivatives and evaluation of their cytotoxic effects on human cancer cells
inferred← citeshttps://doi.org/10.70675/03ff1123ze99dz4c60z8dc3z268abd7e91d4openalex-snapshot
Développement de nouvelles sondes photoactivables pour la caractérisation des cibles cellulaires du glutathion
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