These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 24036392)

  • 1. Differential O-3/O-4 selectivity in the glycosylation of N-dimethylmaleoyl-protected hexosamine acceptors: effect of a conformationally armed (superarmed) glycosyl donor.
    Della Felice F; Rúveda EA; Stortz CA; Colombo MI
    Carbohydr Res; 2013 Oct; 380():167-73. PubMed ID: 24036392
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differential O-3/O-4 regioselectivity in the glycosylation of alpha and beta anomers of 6-O-substituted N-dimethylmaleoyl-protected D-glucosamine acceptors.
    Bohn ML; Colombo MI; Pisano PL; Stortz CA; Rúveda EA
    Carbohydr Res; 2007 Dec; 342(17):2522-36. PubMed ID: 17880931
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Conformational and electronic effects on the regioselectivity of the glycosylation of different anomers of N-dimethylmaleoyl-protected glucosamine acceptors.
    Bohn ML; Colombo MI; Rúveda EA; Stortz CA
    Org Biomol Chem; 2008 Feb; 6(3):554-61. PubMed ID: 18219427
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regioselectivity of the glycosylation of N-dimethylmaleoyl-protected hexosamine acceptors. An experimental and DFT approach.
    Colombo MI; Rúveda EA; Stortz CA
    Org Biomol Chem; 2011 Apr; 9(8):3020-5. PubMed ID: 21380458
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A comparative study of the O-3 reactivity of isomeric N-dimethylmaleoyl-protected D-glucosamine and D-allosamine acceptors.
    Colombo MI; Stortz CA; Rúveda EA
    Carbohydr Res; 2011 Apr; 346(5):569-76. PubMed ID: 21320701
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Armed-disarmed effects in carbohydrate chemistry: history, synthetic and mechanistic studies.
    Fraser-Reid B; López JC
    Top Curr Chem; 2011; 301():1-29. PubMed ID: 21120714
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. Application of the superarmed glycosyl donor to chemoselective oligosaccharide synthesis.
    Mydock LK; Demchenko AV
    Org Lett; 2008 Jun; 10(11):2107-10. PubMed ID: 18447362
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Is an acyl group at O-3 in glucosyl donors able to control α-stereoselectivity of glycosylation? The role of conformational mobility and the protecting group at O-6.
    Komarova BS; Orekhova MV; Tsvetkov YE; Nifantiev NE
    Carbohydr Res; 2014 Jan; 384():70-86. PubMed ID: 24368161
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Orthoesters formation leading to mismatched Helferich glycosylations at O-3 of N-trichloroacetylated glucosamine residues.
    Forman A; Auzanneau FI
    Carbohydr Res; 2016 Apr; 425():10-21. PubMed ID: 27015141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Glycosylation studies on conformationally restricted 3,5-O-(di-tert-butylsilylene)-D-galactofuranosyl trichloroacetimidate donors for 1,2-cis α-D-galactofuranosylation.
    Tilve MJ; Gallo-Rodriguez C
    Carbohydr Res; 2011 Dec; 346(18):2838-48. PubMed ID: 22050997
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot.
    Bandara MD; Yasomanee JP; Rath NP; Pedersen CM; Bols M; Demchenko AV
    Org Biomol Chem; 2017 Jan; 15(3):559-563. PubMed ID: 27942674
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rhamnosylation: diastereoselectivity of conformationally armed donors.
    Heuckendorff M; Pedersen CM; Bols M
    J Org Chem; 2012 Jul; 77(13):5559-68. PubMed ID: 22639871
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 6-O-Benzyl- and 6-O-silyl-N-acetyl-2-amino-2-N,3-O-carbonyl-2-deoxyglucosides: effective glycosyl acceptors in the glucosamine 4-OH Series. effect of anomeric stereochemistry on the removal of the oxazolidinone group.
    Crich D; Vinod AU
    J Org Chem; 2005 Feb; 70(4):1291-6. PubMed ID: 15704963
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Substrate specificity of N-acetylhexosaminidase from Aspergillus oryzae to artificial glycosyl acceptors having various substituents at the reducing ends.
    Ogata M; Zeng X; Usui T; Uzawa H
    Carbohydr Res; 2007 Jan; 342(1):23-30. PubMed ID: 17145046
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. Relevance of the glycosyl donor to the regioselectivity of glycosidation of primary-secondary diol acceptors and application of these ideas to in situ three-component double differential glycosidation.
    Uriel C; Agocs A; Gómez AM; López JC; Fraser-Reid B
    Org Lett; 2005 Oct; 7(22):4899-902. PubMed ID: 16235917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 341(10):1708-16. PubMed ID: 16616900
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Conformationally restricted 3,5-O-(di-tert-butylsilylene)-D-galactofuranosyl thioglycoside donor for 1,2-cis α-D-galactofuranosylation.
    Tilve MJ; Gallo-Rodriguez C
    Carbohydr Res; 2014 Oct; 397():7-17. PubMed ID: 25168009
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Studies on the stereoselective synthesis of a protected α-D-Gal-(1→2)-D-Glc fragment.
    Chen L; Shi SD; Liu YQ; Gao QJ; Yi X; Liu KK; Liu H
    Carbohydr Res; 2011 Jul; 346(10):1250-6. PubMed ID: 21550022
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.