BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

416 related articles for article (PubMed ID: 15787969)

  • 1. Use of the excluded protecting group (EPG) method for peptide synthesis.
    Head DB; Dong JZ; Burton JA
    J Pept Res; 2005 Mar; 65(3):384-94. PubMed ID: 15787969
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Orthogonal protecting groups for N(alpha)-amino and C-terminal carboxyl functions in solid-phase peptide synthesis.
    Albericio F
    Biopolymers; 2000; 55(2):123-39. PubMed ID: 11074410
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Preparation, isolation, and characterization of Nalpha-Fmoc-peptide isocyanates: solution synthesis of oligo-alpha-peptidyl ureas.
    Sureshbabu VV; Patil BS; Venkataramanarao R
    J Org Chem; 2006 Sep; 71(20):7697-705. PubMed ID: 16995676
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Automated peptide-resin deprotection/cleavage by a robotic workstation.
    Zuckermann RN; Banville SC
    Pept Res; 1992; 5(3):169-74. PubMed ID: 1421806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Problem of aspartimide formation in Fmoc-based solid-phase peptide synthesis using Dmab group to protect side chain of aspartic acid.
    Ruczyński J; Lewandowska B; Mucha P; Rekowski P
    J Pept Sci; 2008 Mar; 14(3):335-41. PubMed ID: 17975850
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Side-chain anchoring strategy for solid-phase synthesis of peptide acids with C-terminal cysteine.
    Barany G; Han Y; Hargittai B; Liu RQ; Varkey JT
    Biopolymers; 2003; 71(6):652-66. PubMed ID: 14991675
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New heterocyclic beta-sheet ligands with peptidic recognition elements.
    Rzepecki P; Gallmeier H; Geib N; Cernovska K; König B; Schrader T
    J Org Chem; 2004 Aug; 69(16):5168-78. PubMed ID: 15287758
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Liquid-phase peptide synthesis on polyethylene glycol (PEG) supports using strategies based on the 9-fluorenylmethoxycarbonyl amino protecting group: application of PEGylated peptides in biochemical assays.
    Fischer PM; Zheleva DI
    J Pept Sci; 2002 Sep; 8(9):529-42. PubMed ID: 12371706
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The use of crown ethers in peptide chemistry-V. Solid-phase synthesis of peptides by the fragment condensation approach using crown ethers as non-covalent protecting groups.
    Botti P; Ball HL; Lucietto P; Pinori M; Rizzi E; Mascagni P
    J Pept Sci; 1996; 2(6):371-80. PubMed ID: 9230465
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Edman degradation sequence analysis of resin-bound peptides synthesized by 9-fluorenylmethoxycarbonyl chemistry.
    Fields CG; VanDrisse VL; Fields GB
    Pept Res; 1993; 6(1):39-47. PubMed ID: 8439735
    [TBL] [Abstract][Full Text] [Related]  

  • 11. p-Nitrobenzyl side-chain protection for solid-phase synthesis.
    Hocker MD; Caldwell CG; Macsata RW; Lyttle MH
    Pept Res; 1995; 8(6):310-15. PubMed ID: 8838413
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Incomplete TFA deprotection of N-terminal trityl-asparagine residue in fmoc solid-phase peptide chemistry.
    Friede M; Denery S; Neimark J; Kieffer S; Gausepohl H; Briand JP
    Pept Res; 1992; 5(3):145-7. PubMed ID: 1421802
    [TBL] [Abstract][Full Text] [Related]  

  • 13. N-->O-Acyl shift in Fmoc-based synthesis of phosphopeptides.
    Eberhard H; Seitz O
    Org Biomol Chem; 2008 Apr; 6(8):1349-55. PubMed ID: 18385841
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Solid-Phase synthesis of a dendritic peptide related to a retinoblastoma protein fragment utilizing a combined boc- and fmoc-chemistry approach.
    Cavallaro V; Thompson P; Hearn M
    J Pept Sci; 2001 May; 7(5):262-9. PubMed ID: 11428547
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of cotton as a carrier for solid-phase peptide synthesis.
    Eichler J; Bienert M; Stierandova A; Lebl M
    Pept Res; 1991; 4(5):296-307. PubMed ID: 1802241
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Convenient synthesis of N-methylamino acids compatible with Fmoc solid-phase peptide synthesis.
    Biron E; Kessler H
    J Org Chem; 2005 Jun; 70(13):5183-9. PubMed ID: 15960522
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Dde resin based strategy for inverse solid-phase synthesis of amino terminated peptides, peptide mimetics and protected peptide intermediates.
    Rai A; Gutheil WG
    J Pept Sci; 2005 Feb; 11(2):69-73. PubMed ID: 15635629
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A safety catch linker for Fmoc-based assembly of constrained cyclic peptides.
    Ravn J; Bourne GT; Smythe ML
    J Pept Sci; 2005 Sep; 11(9):572-8. PubMed ID: 15742335
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Preparation of protected peptidyl thioester intermediates for native chemical ligation by Nalpha-9-fluorenylmethoxycarbonyl (Fmoc) chemistry: considerations of side-chain and backbone anchoring strategies, and compatible protection for N-terminal cysteine.
    Gross CM; Lelièvre D; Woodward CK; Barany G
    J Pept Res; 2005 Mar; 65(3):395-410. PubMed ID: 15787970
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Solid-phase synthesis of extended lactam ring systems: preparation of amino acid alpha-fluorenylmethyl esters for the synthesis of reverse-extended lactams.
    Zhao Z; Felix AM
    Pept Res; 1994; 7(4):218-23. PubMed ID: 7696841
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.