BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 12860423)

  • 1. Environmentally benign and stereoselective formation of beta-mannosidic linkages utilizing 2,3-di-O-benzyl-4,6-O-benzylidene-protected mannopyranosyl phosphite and montmorillonite K-10.
    Nagai H; Matsumura S; Toshima K
    Carbohydr Res; 2003 Jul; 338(15):1531-4. PubMed ID: 12860423
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Environmentally benign beta-stereoselective glycosidations of glycosyl phosphites using a reusable heterogeneous solid acid, montmorillonite K-10.
    Nagai H; Sasaki K; Matsumura S; Toshima K
    Carbohydr Res; 2005 Feb; 340(3):337-53. PubMed ID: 15680589
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Is donor-acceptor hydrogen bonding necessary for 4,6-O-benzylidene-directed beta-mannopyranosylation? Stereoselective synthesis of beta-C-mannopyranosides and alpha-C-glucopyranosides.
    Crich D; Sharma I
    Org Lett; 2008 Nov; 10(21):4731-4. PubMed ID: 18826233
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 4,6-O-benzylidene-directed beta-mannopyranosylation and alpha-glucopyranosylation: the 2-deoxy-2-fluoro and 3-deoxy-3-fluoro series of donors and the importance of the O2-C2-C3-O3 interaction.
    Crich D; Li L
    J Org Chem; 2007 Mar; 72(5):1681-90. PubMed ID: 17266375
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Influence of protecting groups on the anomeric equilibrium; case of the 4,6-O-benzylidene acetal in the mannopyranose series.
    Sharma I; Bohé L; Crich D
    Carbohydr Res; 2012 Aug; 357():126-31. PubMed ID: 22739244
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Influence of protecting groups on the reactivity and selectivity of glycosylation: chemistry of the 4,6-o-benzylidene protected mannopyranosyl donors and related species.
    Aubry S; Sasaki K; Sharma I; Crich D
    Top Curr Chem; 2011; 301():141-88. PubMed ID: 21240602
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Stereoselective C-glycoside formation with 2-O-benzyl-4,6-O-benzylidene protected 3-deoxy gluco- and mannopyranoside donors: comparison with O-glycoside formation.
    Moumé-Pymbock M; Crich D
    J Org Chem; 2012 Oct; 77(20):8905-12. PubMed ID: 23009024
    [TBL] [Abstract][Full Text] [Related]  

  • 8. On the influence of the C2-O2 and C3-O3 bonds in 4,6-O-benzylidene-directed beta-mannopyranosylation and alpha-glucopyranosylation.
    Crich D; Vinogradova O
    J Org Chem; 2006 Oct; 71(22):8473-80. PubMed ID: 17064022
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Influence of O6 in mannosylations using benzylidene protected donors: stereoelectronic or conformational effects?
    Frihed TG; Walvoort MT; Codée JD; van der Marel GA; Bols M; Pedersen CM
    J Org Chem; 2013 Mar; 78(6):2191-205. PubMed ID: 23336427
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Asymmetric Organocatalytic Reductive Coupling Reactions between Benzylidene Pyruvates and Aldehydes.
    Horwitz MA; Zavesky BP; Martinez-Alvarado JI; Johnson JS
    Org Lett; 2016 Jan; 18(1):36-9. PubMed ID: 26667068
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Regioselective and stereoselective benzylidene installation and one-pot protection of D-mannose.
    Patil PS; Lee CC; Huang YW; Zulueta MM; Hung SC
    Org Biomol Chem; 2013 Apr; 11(16):2605-12. PubMed ID: 23446759
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Determination of the Influence of Side-Chain Conformation on Glycosylation Selectivity using Conformationally Restricted Donors.
    Dharuman S; Crich D
    Chemistry; 2016 Mar; 22(13):4535-42. PubMed ID: 26880055
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 2-(Hydroxycarbonyl)benzyl glycosides: a novel type of glycosyl donors for highly efficient beta-mannopyranosylation and oligosaccharide synthesis by latent-active glycosylation.
    Kim KS; Kim JH; Lee YJ; Lee YJ; Park J
    J Am Chem Soc; 2001 Sep; 123(35):8477-81. PubMed ID: 11525654
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Highly diastereoselective alpha-mannopyranosylation in the absence of participating protecting groups.
    Crich D; Cai W; Dai Z
    J Org Chem; 2000 Mar; 65(5):1291-7. PubMed ID: 10814088
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis of three tetrasaccharides containing 3-O-methyl-D-mannose, as model compounds for xylose-containing carbohydrate chains from N-glycoproteins.
    van der Ven JG; Wijkmans JC; Kamerling JP; Vliegenthart JF
    Carbohydr Res; 1994 Feb; 253():121-39. PubMed ID: 8156544
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of an octasaccharide fragment of high-mannose-type glycans of glycoproteins.
    Nukada T; Kitajima T; Nakahara Y; Ogawa T
    Carbohydr Res; 1992 Apr; 228(1):157-70. PubMed ID: 1516084
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stereoselective synthesis of 2,3-diamino-2,3-dideoxy-β-D-mannopyranosyl uronates.
    Walvoort MT; Moggré GJ; Lodder G; Overkleeft HS; Codée JD; van der Marel GA
    J Org Chem; 2011 Sep; 76(18):7301-15. PubMed ID: 21793528
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Influence of the O3 protecting group on stereoselectivity in the preparation of C-mannopyranosides with 4,6-O-benzylidene protected donors.
    Crich D; Sharma I
    J Org Chem; 2010 Dec; 75(24):8383-91. PubMed ID: 21070063
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 2-O-propargyl ethers: readily cleavable, minimally intrusive protecting groups for beta-mannosyl donors.
    Crich D; Jayalath P
    Org Lett; 2005 May; 7(11):2277-80. PubMed ID: 15901188
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Glycosylation with 2-Acetamido-2-deoxyglycosyl Donors at a Low Temperature: Scope of the Non-Oxazoline Method.
    Arihara R; Kakita K; Suzuki N; Nakamura S; Hashimoto S
    J Org Chem; 2015 May; 80(9):4259-77. PubMed ID: 25807142
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.