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 *

495 related articles for article (PubMed ID: 20121053)

  • 21. Multigram-scale synthesis of short peptides via a simplified repetitive solution-phase procedure.
    Meneses C; Nicoll SL; Trembleau L
    J Org Chem; 2010 Feb; 75(3):564-9. PubMed ID: 20043628
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Nitrone protecting groups for enantiopure N-hydroxyamino acids: synthesis of N-terminal peptide hydroxylamines for chemoselective ligations.
    Medina SI; Wu J; Bode JW
    Org Biomol Chem; 2010 Aug; 8(15):3405-17. PubMed ID: 20567784
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An efficient synthesis of N-methyl amino acids by way of intermediate 5-oxazolidinones.
    Aurelio L; Box JS; Brownlee RT; Hughes AB; Sleebs MM
    J Org Chem; 2003 Apr; 68(7):2652-67. PubMed ID: 12662035
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Synthetic strategy for side chain mono-N-alkylation of Fmoc-amino acids promoted by molecular sieves.
    Monfregola L; De Luca S
    Amino Acids; 2011 Oct; 41(4):981-90. PubMed ID: 21069398
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. A gentle method for linking Tris to amino acids and peptides.
    Whittaker RG; Hayes PJ; Bender VJ
    Pept Res; 1993; 6(3):125-8. PubMed ID: 8318742
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 2-(N-Fmoc)-3-(N-Boc-N-methoxy)-diaminopropanoic acid, an amino acid for the synthesis of mimics of O-linked glycopeptides.
    Carrasco MR; Brown RT; Doan VH; Kandel SM; Lee FC
    Biopolymers; 2006; 84(4):414-20. PubMed ID: 16508952
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The world of beta- and gamma-peptides comprised of homologated proteinogenic amino acids and other components.
    Seebach D; Beck AK; Bierbaum DJ
    Chem Biodivers; 2004 Aug; 1(8):1111-239. PubMed ID: 17191902
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Proteinogenic amino acids labelled with 15N and/or 13C for application in peptide synthesis: a short review with a comprehensive list of published derivatives.
    Ragnarsson U
    J Pept Sci; 1995; 1(3):149-56. PubMed ID: 9222992
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Continuous-flow solid (gel)-phase peptide synthesis using unsupported ultrahigh-load polymers: Fmoc/t-butyl strategy.
    Johnson T; Coffey AF
    Pept Res; 1993; 6(6):337-45. PubMed ID: 8292851
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Optimized selective N-methylation of peptides on solid support.
    Biron E; Chatterjee J; Kessler H
    J Pept Sci; 2006 Mar; 12(3):213-9. PubMed ID: 16189816
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [A transformylation reaction--transfer of an N-formyl residue to amino acids and peptides in nucleophilic groups--as a side reaction of peptide synthesis].
    Kotlova EK; Levin ED; Iusupova MP; Rozynov BV; Stepanov VM
    Bioorg Khim; 1994 Nov; 20(11):1186-95. PubMed ID: 7880178
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Synthesis of differentially protected N-acylated reduced pseudodipeptides as building units for backbone cyclic peptides.
    Besser D; Müller B; Agricola I; Reissmann S
    J Pept Sci; 2000 Mar; 6(3):130-8. PubMed ID: 10759211
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel N omega-xanthenyl-protecting groups for asparagine and glutamine, and applications to N alpha-9-fluorenylmethyloxycarbonyl (Fmoc) solid-phase peptide synthesis.
    Han Y; Solé NA; Tejbrant J; Barany G
    Pept Res; 1996; 9(4):166-73. PubMed ID: 8914163
    [TBL] [Abstract][Full Text] [Related]  

  • 38. An efficient conversion of the carboxylic group of N-Fmoc alpha-amino acids/peptide acids into N-formamides employing isocyanates as key intermediates.
    Sudarshan NS; Narendra N; Hemantha HP; Sureshbabu VV
    J Org Chem; 2007 Dec; 72(25):9804-7. PubMed ID: 17999520
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Site-selective methylation of N(beta)-nosyl hydrazides of N-nosyl protected alpha-amino acids.
    De Marco R; Leggio A; Liguori A; Marino T; Perri F; Russo N
    J Org Chem; 2010 May; 75(10):3381-6. PubMed ID: 20405869
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 25.