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Journal Abstract Search

388 related items for PubMed ID: 27912141

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Cationic gold(I)-catalyzed glycosylation with glycosyl N-1,1-dimethylpropargyl carbamate donors.
    Gurung PB, Thapa P, Hettiarachchi IL, Zhu J.
    Org Biomol Chem; 2022 Sep 14; 20(35):7006-7010. PubMed ID: 36000552
    [Abstract] [Full Text] [Related]

  • 3. Bromodimethylsulfonium bromide/silver triflate-promoted glycosylations using glycosyl allenoates as donors.
    Zhang Y, Wang P, Song N, Li M.
    Carbohydr Res; 2013 Nov 15; 381():101-11. PubMed ID: 24095942
    [Abstract] [Full Text] [Related]

  • 4. Development of the Pictet-Spengler reaction catalyzed by AuCl3/AgOTf.
    Youn SW.
    J Org Chem; 2006 Mar 17; 71(6):2521-3. PubMed ID: 16526809
    [Abstract] [Full Text] [Related]

  • 5. An unusual glycosylation product from a partially protected fucosyl donor under silver triflate activation conditions.
    Daly R, Scanlan EM.
    Org Biomol Chem; 2013 Dec 28; 11(48):8452-7. PubMed ID: 24201894
    [Abstract] [Full Text] [Related]

  • 6. Synthesis of 2,3,6-trideoxysugar-containing disaccharides by cyclization and glycosidation through the sequential activation of sulfoxide and methylsulfanyl groups in a one-pot procedure.
    Amaya T, Takahashi D, Tanaka H, Takahashi T.
    Angew Chem Int Ed Engl; 2003 Apr 25; 42(16):1833-6. PubMed ID: 12722074
    [No Abstract] [Full Text] [Related]

  • 7. A glycosylation protocol based on activation of glycosyl 2-pyridyl sulfones with samarium triflate.
    Chang GX, Lowary TL.
    Org Lett; 2000 Jun 01; 2(11):1505-8. PubMed ID: 10841465
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  • 11. Evaluation of thioglycosides of Kdo as glycosyl donors.
    Mannerstedt K, Ekelöf K, Oscarson S.
    Carbohydr Res; 2007 Feb 26; 342(3-4):631-7. PubMed ID: 17027943
    [Abstract] [Full Text] [Related]

  • 12. Revisit of the phenol O-glycosylation with glycosyl imidates, BF₃·OEt₂ is a better catalyst than TMSOTf.
    Li Y, Mo H, Lian G, Yu B.
    Carbohydr Res; 2012 Dec 01; 363():14-22. PubMed ID: 23103509
    [Abstract] [Full Text] [Related]

  • 13. An efficient and selective method for preparing glycosyl sulfoxides by oxidizing glycosyl sulfides with OXONE or t-BuOOH on SiO2.
    Chen MY, Patkar LN, Chen HT, Lin CC.
    Carbohydr Res; 2003 Jun 16; 338(12):1327-32. PubMed ID: 12791287
    [Abstract] [Full Text] [Related]

  • 14. 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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  • 16. Highly stereoselective glycosyl-chloride-mediated synthesis of 2-deoxyglucosides.
    Verma VP, Wang CC.
    Chemistry; 2013 Jan 14; 19(3):846-51. PubMed ID: 23233443
    [Abstract] [Full Text] [Related]

  • 17. Conformationally armed 3,6-tethered glycosyl donors: synthesis, conformation, reactivity, and selectivity.
    Heuckendorff M, Pedersen CM, Bols M.
    J Org Chem; 2013 Jul 19; 78(14):7234-48. PubMed ID: 23786671
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. ortho-(Methyltosylaminoethynyl)benzyl glycosides as new glycosyl donors for latent-active glycosylation.
    Chen X, Shen D, Wang Q, Yang Y, Yu B.
    Chem Commun (Camb); 2015 Sep 21; 51(73):13957-60. PubMed ID: 26243539
    [Abstract] [Full Text] [Related]

  • 20. Taming the Reactivity of Glycosyl Iodides To Achieve Stereoselective Glycosidation.
    Gervay-Hague J.
    Acc Chem Res; 2016 Jan 19; 49(1):35-47. PubMed ID: 26524481
    [Abstract] [Full Text] [Related]

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