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Journal Abstract Search

195 related items for PubMed ID: 36000552

  • 1.
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  • 3. AuCl3-AgOTf promoted O-glycosylation using anomeric sulfoxides as glycosyl donors at room temperature.
    Palanivel A, Chennaiah A, Dubbu S, Mallick A, Vankar YD.
    Carbohydr Res; 2017 Jan 02; 437():43-49. PubMed ID: 27912141
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  • 4. Highly Reactive Glycosylation with 1-O-(Methylthio)thiocarbonyl Glycosyl Donors under Acidic to Neutral Reaction Conditions.
    Luo T, Zhang GH, Guo YF, Dong H.
    J Org Chem; 2024 Oct 04; 89(19):14315-14327. PubMed ID: 39268645
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  • 5. o-(p-Methoxyphenylethynyl)phenyl Glycosides: Versatile New Glycosylation Donors for the Highly Efficient Construction of Glycosidic Linkages.
    Hu Y, Yu K, Shi LL, Liu L, Sui JJ, Liu DY, Xiong B, Sun JS.
    J Am Chem Soc; 2017 Sep 13; 139(36):12736-12744. PubMed ID: 28835100
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  • 6. Fe(III)-catalyzed stereoselective synthesis of deoxyglycosides using stable bifunctional deoxy-phenylpropiolate glycoside donors.
    Aghi A, Sau S, Kumar A.
    Carbohydr Res; 2024 Feb 13; 536():109051. PubMed ID: 38325069
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  • 7. Activation of glycosyl methylpropiolates by TfOH.
    Walke G, Kasdekar N, Pati S, Taillefer M, Jaroschik F, Hotha S.
    Carbohydr Res; 2024 May 13; 539():109106. PubMed ID: 38640704
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  • 9. Stereodirecting Effect of C5-Carboxylate Substituents on the Glycosylation Stereochemistry of 3-Deoxy-d- manno-oct-2-ulosonic Acid (Kdo) Thioglycoside Donors: Stereoselective Synthesis of α- and β-Kdo Glycosides.
    Huang W, Zhou YY, Pan XL, Zhou XY, Lei JC, Liu DM, Chu Y, Yang JS.
    J Am Chem Soc; 2018 Mar 14; 140(10):3574-3582. PubMed ID: 29481074
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  • 13. Glycosyl trichloroacetylcarbamate: a new glycosyl donor for O-glycosylation.
    Jayakanthan K, Vankar YD.
    Carbohydr Res; 2005 Dec 12; 340(17):2688-92. PubMed ID: 16212950
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  • 14. Gold(I)-Catalyzed Glycosylation with Glycosyl o-Alkynylbenzoates as Donors.
    Yu B.
    Acc Chem Res; 2018 Feb 20; 51(2):507-516. PubMed ID: 29297680
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  • 15. Electron-deficient pyridinium salts/thiourea cooperative catalyzed O-glycosylation via activation of O-glycosyl trichloroacetimidate donors.
    Shaw M, Kumar Y, Thakur R, Kumar A.
    Beilstein J Org Chem; 2017 Feb 20; 13():2385-2395. PubMed ID: 29181119
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  • 16. Glycosyl 3-Phenyl-4-pentenoates as Versatile Glycosyl Donors: Reactivity and Their Application in One-Pot Oligosaccharide Assemblies.
    Javed, Khanam A, Mandal PK.
    J Org Chem; 2022 May 20; 87(10):6710-6729. PubMed ID: 35522927
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  • 17. Mild method for the synthesis of α-glycosyl chlorides: A convenient protocol for quick one-pot glycosylation.
    Khanam A, Dubey S, Mandal PK.
    Carbohydr Res; 2023 Dec 20; 534():108976. PubMed ID: 37871478
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  • 18. Synthesis of disaccharide nucleosides by the O-glycosylation of natural nucleosides with thioglycoside donors.
    Aoki S, Fukumoto T, Itoh T, Kurihara M, Saito S, Komabiki SY.
    Chem Asian J; 2015 Mar 20; 10(3):740-51. PubMed ID: 25677492
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  • 19. Pyranosides with 2,3-trans carbamate groups: exocyclic or endocyclic cleavage reaction?
    Manabe S, Ito Y.
    Chem Rec; 2014 Jun 20; 14(3):502-15. PubMed ID: 24914008
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  • 20. Gold(I)-catalyzed glycosylation with glycosyl ortho-alkynylbenzoates as donors: general scope and application in the synthesis of a cyclic triterpene saponin.
    Li Y, Yang X, Liu Y, Zhu C, Yang Y, Yu B.
    Chemistry; 2010 Feb 08; 16(6):1871-82. PubMed ID: 20039348
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