BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 14680246)

  • 1. Rapid synthesis of oligosaccharides using an anomeric fluorous silyl protecting group.
    Manzoni L
    Chem Commun (Camb); 2003 Dec; (23):2930-1. PubMed ID: 14680246
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Froc: a new fluorous protective group for peptide and oligosaccharide synthesis.
    Manzoni L; Castelli R
    Org Lett; 2006 Mar; 8(5):955-7. PubMed ID: 16494483
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of the Lewis a trisaccharide based on an anomeric silyl fluorous tag.
    Manzoni L; Castelli R
    Org Lett; 2004 Nov; 6(23):4195-8. PubMed ID: 15524441
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid oligosaccharide synthesis using a fluorous protective group.
    Miura T; Goto K; Waragai H; Matsumoto H; Hirose Y; Ohmae M; Ishida HK; Satoh A; Inazu T
    J Org Chem; 2004 Aug; 69(16):5348-53. PubMed ID: 15287781
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fluorous-assisted chemoenzymatic synthesis of heparan sulfate oligosaccharides.
    Cai C; Dickinson DM; Li L; Masuko S; Suflita M; Schultz V; Nelson SD; Bhaskar U; Liu J; Linhardt RJ
    Org Lett; 2014 Apr; 16(8):2240-3. PubMed ID: 24697306
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fluorous-tag assisted synthesis of a glycosaminoglycan mimetic tetrasaccharide as a high-affinity FGF-2 and midkine ligand.
    Maza S; Gandia-Aguado N; de Paz JL; Nieto PM
    Bioorg Med Chem; 2018 Mar; 26(5):1076-1085. PubMed ID: 29409708
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluorous-tagged compound: a viable scaffold to prime oligosaccharide synthesis by cellular enzymes.
    Kasuya MC; Cusi R; Ishihara O; Miyagawa A; Hashimoto K; Sato T; Hatanaka K
    Biochem Biophys Res Commun; 2004 Apr; 316(3):599-604. PubMed ID: 15033442
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Assembly of a Complex Branched Oligosaccharide by Combining Fluorous-Supported Synthesis and Stereoselective Glycosylations using Anomeric Sulfonium Ions.
    Huang W; Gao Q; Boons GJ
    Chemistry; 2015 Sep; 21(37):12920-6. PubMed ID: 26250358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fluorous supported modular synthesis of heparan sulfate oligosaccharides.
    Zong C; Venot A; Dhamale O; Boons GJ
    Org Lett; 2013 Jan; 15(2):342-5. PubMed ID: 23293947
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Toward solution-phase automated iterative synthesis: fluorous-tag assisted solution-phase synthesis of linear and branched mannose oligomers.
    Jaipuri FA; Pohl NL
    Org Biomol Chem; 2008 Aug; 6(15):2686-91. PubMed ID: 18633525
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Automated fluorous-assisted solution-phase synthesis of β-1,2-, 1,3-, and 1,6-mannan oligomers.
    Tang SL; Pohl NLB
    Carbohydr Res; 2016 Jul; 430():8-15. PubMed ID: 27155895
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fluorous tagging strategy for solution-phase synthesis of small molecules, peptides and oligosaccharides.
    Zhang W
    Curr Opin Drug Discov Devel; 2004 Nov; 7(6):784-97. PubMed ID: 15595439
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fluorous-Tag Assisted Syntheses of Sulfated Keratan Sulfate Oligosaccharide Fragments.
    Bhaduri S; Pohl NL
    Org Lett; 2016 Mar; 18(6):1414-7. PubMed ID: 26958998
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differently complex oligosaccharides can be easily identified by matrix-assisted laser desorption and ionization time-of-flight mass spectrometry directly from a standard thin-layer chromatography plate.
    Nimptsch K; Süss R; Riemer T; Nimptsch A; Schnabelrauch M; Schiller J
    J Chromatogr A; 2010 Jun; 1217(23):3711-5. PubMed ID: 20434160
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fluorous-Tag-Assisted Synthesis of GAG-Like Oligosaccharides.
    de Paz JL; Nieto PM
    Methods Mol Biol; 2022; 2303():37-47. PubMed ID: 34626368
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of fluorous photolabile aldehyde and carbamate and alkyl carbamate protecting groups for carbohydrate-associated amines.
    Roychoudhury R; Pohl NL
    Org Lett; 2014 Feb; 16(4):1156-9. PubMed ID: 24512452
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fluorous Boc ((F)Boc) carbamates: new amine protecting groups for use in fluorous synthesis.
    Luo Z; Williams J; Read RW; Curran DP
    J Org Chem; 2001 Jun; 66(12):4261-6. PubMed ID: 11397162
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hydrophobically assisted switching phase synthesis: the flexible combination of solid-phase and solution-phase reactions employed for oligosaccharide preparation.
    Bauer J; Rademann J
    J Am Chem Soc; 2005 May; 127(20):7296-7. PubMed ID: 15898762
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of native milk oligosaccharides directly from thin-layer chromatography plates by matrix-assisted laser desorption/ionization orthogonal-time-of-flight mass spectrometry with a glycerol matrix.
    Dreisewerd K; Kölbl S; Peter-Katalinić J; Berkenkamp S; Pohlentz G
    J Am Soc Mass Spectrom; 2006 Feb; 17(2):139-50. PubMed ID: 16412664
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A fluorous phosphate protecting group with applications to carbohydrate synthesis.
    Liu L; Pohl NL
    Org Lett; 2011 Apr; 13(7):1824-7. PubMed ID: 21384825
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.