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Journal Abstract Search


153 related items for PubMed ID: 37871478

  • 1. 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; 534():108976. PubMed ID: 37871478
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  • 2. Synthesis of glycosyl chlorides using catalytic Appel conditions.
    Pongener I, Nikitin K, McGarrigle EM.
    Org Biomol Chem; 2019 Aug 28; 17(32):7531-7535. PubMed ID: 31369028
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  • 3. Solvent-free, under air selective synthesis of α-glycosides adopting glycosyl chlorides as donors.
    Traboni S, Vessella G, Bedini E, Iadonisi A.
    Org Biomol Chem; 2020 Jul 15; 18(27):5157-5163. PubMed ID: 32583825
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  • 8. Nickel-catalyzed stereoselective glycosylation with C(2)-N-substituted benzylidene D-glucosamine and galactosamine trichloroacetimidates for the formation of 1,2-cis-2-amino glycosides. Applications to the synthesis of heparin disaccharides, GPI anchor pseudodisaccharides, and α-GalNAc.
    Mensah EA, Yu F, Nguyen HM.
    J Am Chem Soc; 2010 Oct 13; 132(40):14288-302. PubMed ID: 20860359
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  • 9. 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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  • 12. Iron(III) chloride as an efficient catalyst for stereoselective synthesis of glycosyl azides and a cocatalyst with Cu(0) for the subsequent click chemistry.
    Salunke SB, Babu NS, Chen CT.
    Chem Commun (Camb); 2011 Oct 07; 47(37):10440-2. PubMed ID: 21842053
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  • 13. 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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  • 18. Iron(iii) chloride-catalyzed activation of glycosyl chlorides.
    Geringer SA, Demchenko AV.
    Org Biomol Chem; 2018 Dec 05; 16(47):9133-9137. PubMed ID: 30430182
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