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Journal Abstract Search

129 related items for PubMed ID: 17253751

  • 1. Chemoselective synthesis of oligosaccharides of 2-deoxy-2-aminosugars.
    Bongat AF, Kamat MN, Demchenko AV.
    J Org Chem; 2007 Feb 16; 72(4):1480-3. PubMed ID: 17253751
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  • 2. Revisiting the armed-disarmed concept rationale: s-benzoxazolyl glycosides in chemoselective oligosaccharide synthesis.
    Kamat MN, Demchenko AV.
    Org Lett; 2005 Jul 21; 7(15):3215-8. PubMed ID: 16018624
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  • 3. Comparison of the armed/disarmed building blocks of the D-gluco and D-glucosamino series in the context of chemoselective oligosaccharide synthesis.
    Kamkhachorn T, Parameswar AR, Demchenko AV.
    Org Lett; 2010 Jul 02; 12(13):3078-81. PubMed ID: 20527789
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  • 4. How the arming participating moieties can broaden the scope of chemoselective oligosaccharide synthesis by allowing the inverse armed-disarmed approach.
    Smoot JT, Demchenko AV.
    J Org Chem; 2008 Nov 21; 73(22):8838-50. PubMed ID: 18939875
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  • 5. S-thiazolinyl (STaz) glycosides as versatile building blocks for convergent selective, chemoselective, and orthogonal oligosaccharide synthesis.
    Pornsuriyasak P, Demchenko AV.
    Chemistry; 2006 Aug 25; 12(25):6630-46. PubMed ID: 16800023
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  • 9. Preparation of oligosaccharide units library and its utilization.
    Murata T, Usui T.
    Biosci Biotechnol Biochem; 1997 Jul 25; 61(7):1059-66. PubMed ID: 9255967
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  • 10. 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
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  • 13. Chemoselective activation of ethyl vs. phenyl thioglycosides: one-pot synthesis of oligosaccharides.
    Mc Carthy C, Zhu X.
    Org Biomol Chem; 2020 Nov 28; 18(44):9029-9034. PubMed ID: 32869806
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  • 14. Application of the superarmed glycosyl donor to chemoselective oligosaccharide synthesis.
    Mydock LK, Demchenko AV.
    Org Lett; 2008 Jun 05; 10(11):2107-10. PubMed ID: 18447362
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  • 15. Stereoselective synthesis of 2-deoxy-2-iodo-glycosides from furanoses. A new route to 2-deoxy-glycosides and 2-deoxy-oligosaccharides of ribo and xylo configuration.
    Rodríguez MA, Boutureira O, Arnés X, Matheu MI, Díaz Y, Castillón S.
    J Org Chem; 2005 Dec 09; 70(25):10297-310. PubMed ID: 16323838
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  • 16. Synthesis of oligosaccharides as potential inhibitors of mycobacterial arabinosyltransferases. Di- and trisaccharides containing C-5 modified arabinofuranosyl residues.
    Cociorva OM, Lowary TL.
    Carbohydr Res; 2004 Mar 15; 339(4):853-65. PubMed ID: 14980829
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  • 17. Gold-catalyzed glycosidation for the synthesis of trisaccharides by applying the armed-disarmed strategy.
    Kayastha AK, Hotha S.
    Beilstein J Org Chem; 2013 Mar 15; 9():2147-55. PubMed ID: 24204427
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  • 18. Installation of electron-donating protective groups, a strategy for glycosylating unreactive thioglycosyl acceptors using the preactivation-based glycosylation method.
    Zeng Y, Wang Z, Whitfield D, Huang X.
    J Org Chem; 2008 Oct 17; 73(20):7952-62. PubMed ID: 18808187
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  • 19. Efficient synthesis of omega-mercaptoalkyl 1,2-trans-glycosides from sugar peracetates.
    Murakami T, Hirono R, Sato Y, Furusawa K.
    Carbohydr Res; 2007 Jun 11; 342(8):1009-20. PubMed ID: 17362892
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  • 20. Simplifying oligosaccharide synthesis: efficient synthesis of lactosamine and siaylated lactosamine oligosaccharide donors.
    Yan F, Mehta S, Eichler E, Wakarchuk WW, Gilbert M, Schur MJ, Whitfield DM.
    J Org Chem; 2003 Mar 21; 68(6):2426-31. PubMed ID: 12636412
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