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PUBMED FOR HANDHELDS

Journal Abstract Search


322 related items for PubMed ID: 23103509

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  • 4. Glycosylation of sialyl acetates with a novel catalyst combination: bismuth triflate and BF3.OEt2 system.
    Ikeda K, Torisawa Y, Nishi T, Minamikawa J, Tanaka K, Sato M.
    Bioorg Med Chem; 2003 Jul 17; 11(14):3073-6. PubMed ID: 12818669
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  • 5. Convenient temporary methyl imidate protection of N-acetylglucosamine and glycosylation at O-4.
    Cheng A, Hendel JL, Colangelo K, Bonin M, Auzanneau FI.
    J Org Chem; 2008 Oct 03; 73(19):7574-9. PubMed ID: 18767802
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  • 6. Nucleophilic substitution at the anomeric position of 1,2-O-isopropylidenefuranose derivatives. A novel stereoselective synthesis of cyclic phosphates analogous to cAMP.
    Romero M, Hernández L, Quintero L, Sartillo-Piscil F.
    Carbohydr Res; 2006 Dec 29; 341(18):2883-90. PubMed ID: 17087924
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  • 7. O-Benzoxazolyl imidates as versatile glycosyl donors for chemical glycosylation.
    Nigudkar SS, Parameswar AR, Pornsuriyasak P, Stine KJ, Demchenko AV.
    Org Biomol Chem; 2013 Jun 28; 11(24):4068-76. PubMed ID: 23674052
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  • 8. Facile TMSOTf-catalyzed preparation of 2-deoxy α-O-aryl-D-glycosides from glycosyl acetates.
    Yang G, Wang Q, Luo X, Zhang J, Tang J.
    Glycoconj J; 2012 Aug 28; 29(5-6):453-6. PubMed ID: 22864908
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  • 9. 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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  • 14. 2'-Carboxybenzyl glycosides: glycosyl donors for C-glycosylation and conversion into other glycosyl donors.
    Lee YJ, Baek JY, Lee BY, Kang SS, Park HS, Jeon HB, Kim KS.
    Carbohydr Res; 2006 Jul 24; 341(10):1708-16. PubMed ID: 16616900
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  • 15. O-Glycosylation methods in the total synthesis of complex natural glycosides.
    Yang Y, Zhang X, Yu B.
    Nat Prod Rep; 2015 Sep 24; 32(9):1331-55. PubMed ID: 26067865
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  • 16. Novel glycosylation of the nitroxyl radicals with peracetylated glycosyl fluorides using a combination of BF(3) x OEt(2) and an amine base as promoters.
    Sato S, Kumazawa T, Matsuba S, Onodera J, Aoyama M, Obara H, Kamada H.
    Carbohydr Res; 2001 Aug 30; 334(3):215-22. PubMed ID: 11513828
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  • 20. Regioselective one-pot protection of glucose.
    Wang CC, Kulkarni SS, Lee JC, Luo SY, Hung SC.
    Nat Protoc; 2008 Aug 30; 3(1):97-113. PubMed ID: 18193026
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