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Journal Abstract Search

218 related items for PubMed ID: 18808187

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

  • 2. Oligosaccharide synthesis with glycosyl phosphate and dithiophosphate triesters as glycosylating agents.
    Plante OJ, Palmacci ER, Andrade RB, Seeberger PH.
    J Am Chem Soc; 2001 Oct 03; 123(39):9545-54. PubMed ID: 11572674
    [Abstract] [Full Text] [Related]

  • 3. ortho-Methylphenylthioglycosides as glycosyl building blocks for preactivation-based oligosaccharide synthesis.
    Peng P, Xiong DC, Ye XS.
    Carbohydr Res; 2014 Jan 30; 384():1-8. PubMed ID: 24334234
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Preactivation-based chemoselective glycosylations: A powerful strategy for oligosaccharide assembly.
    Yang W, Yang B, Ramadan S, Huang X.
    Beilstein J Org Chem; 2017 Jun 05; 13():2094-2114. PubMed ID: 29062430
    [Abstract] [Full Text] [Related]

  • 6. Thio-arylglycosides with various aglycon para-substituents: a probe for studying chemical glycosylation reactions.
    Li X, Huang L, Hu X, Huang X.
    Org Biomol Chem; 2009 Jan 07; 7(1):117-27. PubMed ID: 19081954
    [Abstract] [Full Text] [Related]

  • 7. "Active-latent" thioglycosyl donors and acceptors in oligosaccharide syntheses.
    Shiao TC, Roy R.
    Top Curr Chem; 2011 Jan 07; 301():69-108. PubMed ID: 21298410
    [Abstract] [Full Text] [Related]

  • 8. One-pot oligosaccharide synthesis exploiting solvent reactivity effects.
    Lahmann M, Oscarson S.
    Org Lett; 2000 Nov 30; 2(24):3881-2. PubMed ID: 11101443
    [Abstract] [Full Text] [Related]

  • 9. Combinatorial synthesis of an oligosaccharide library by using beta-bromoglycoside-mediated iterative glycosylation of selenoglycosides: rapid expansion of molecular diversity with simple building blocks.
    Yamago S, Yamada T, Ito H, Hara O, Mino Y, Yoshida J.
    Chemistry; 2005 Oct 21; 11(21):6159-74. PubMed ID: 16075449
    [Abstract] [Full Text] [Related]

  • 10. Donor Preactivation-Based Glycan Assembly: from Manual to Automated Synthesis.
    Yao W, Ye XS.
    Acc Chem Res; 2024 Jun 04; 57(11):1577-1594. PubMed ID: 38623919
    [Abstract] [Full Text] [Related]

  • 11. Multi-component one-pot synthesis of the tumor-associated carbohydrate antigen Globo-H based on preactivation of thioglycosyl donors.
    Wang Z, Zhou L, El-Boubbou K, Ye XS, Huang X.
    J Org Chem; 2007 Aug 17; 72(17):6409-20. PubMed ID: 17658849
    [Abstract] [Full Text] [Related]

  • 12. Mapping the Reactivity and Selectivity of 2-Azidofucosyl Donors for the Assembly of N-Acetylfucosamine-Containing Bacterial Oligosaccharides.
    Hagen B, Ali S, Overkleeft HS, van der Marel GA, Codée JD.
    J Org Chem; 2017 Jan 20; 82(2):848-868. PubMed ID: 28051314
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Use of ionically tagged glycosyl donors in the synthesis of oligosaccharide libraries.
    Kim EJ, Gray GR.
    Bioorg Med Chem Lett; 2009 Dec 01; 19(23):6679-81. PubMed ID: 19837587
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Synthesis of oligosaccharides corresponding to Streptococcus pneumoniae type 9 capsular polysaccharide structures.
    Alpe M, Oscarson S.
    Carbohydr Res; 2002 Oct 11; 337(19):1715-22. PubMed ID: 12423949
    [Abstract] [Full Text] [Related]

  • 19. A novel strategy for oligosaccharide synthesis via temporarily deactivated S-thiazolyl glycosides as glycosyl acceptors.
    Pornsuriyasak P, Gangadharmath UB, Rath NP, Demchenko AV.
    Org Lett; 2004 Nov 25; 6(24):4515-8. PubMed ID: 15548064
    [Abstract] [Full Text] [Related]

  • 20. In situ formation of β-glycosyl imidinium triflate from participating thioglycosyl donors: elaboration to disarmed-armed iterative glycosylation.
    Lin YH, Ghosh B, Mong KK.
    Chem Commun (Camb); 2012 Nov 14; 48(88):10910-2. PubMed ID: 23023321
    [Abstract] [Full Text] [Related]

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