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 *

93 related articles for article (PubMed ID: 561800)

  • 1. Formation and degradation of urea derivatives in the azide method of peptide synthesis. Part 1. The Curtius rearrangement and urea formation.
    Inouye K; Watanabe K; Shin M
    J Chem Soc Perkin 1; 1977; (17):1905-11. PubMed ID: 561800
    [No Abstract]   [Full Text] [Related]  

  • 2. Formation and degradation of urea derivatives in the azide method of peptide synthesis. Part 2. Acidolytic degradation of urea derivatives.
    Inouye K; Watanabe K
    J Chem Soc Perkin 1; 1977; (17):1911-5. PubMed ID: 561801
    [No Abstract]   [Full Text] [Related]  

  • 3. Azide monoliths as convenient flow reactors for efficient Curtius rearrangement reactions.
    Baumann M; Baxendale IR; Ley SV; Nikbin N; Smith CD
    Org Biomol Chem; 2008 May; 6(9):1587-93. PubMed ID: 18421390
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A modular flow reactor for performing Curtius rearrangements as a continuous flow process.
    Baumann M; Baxendale IR; Ley SV; Nikbin N; Smith CD; Tierney JP
    Org Biomol Chem; 2008 May; 6(9):1577-86. PubMed ID: 18421389
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isocyanates of N alpha-[(9-fluorenylmethyl)oxy]carbonyl amino acids: synthesis, isolation, characterization, and application to the efficient synthesis of urea peptidomimetics.
    Patil BS; Vasanthakumar GR; Suresh Babu VV
    J Org Chem; 2003 Sep; 68(19):7274-80. PubMed ID: 12968876
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Curtius rearrangement of aromatic carboxylic acids to access protected anilines and aromatic ureas.
    Lebel H; Leogane O
    Org Lett; 2006 Dec; 8(25):5717-20. PubMed ID: 17134255
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New and simple synthesis of acid azides, ureas and carbamates from carboxylic acids: application of peptide coupling agents EDC and HBTU.
    Sureshbabu VV; Lalithamba HS; Narendra N; Hemantha HP
    Org Biomol Chem; 2010 Feb; 8(4):835-40. PubMed ID: 20135041
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Scalable, One-Pot, Microwave-Accelerated Tandem Synthesis of Unsymmetrical Urea Derivatives.
    Kulkarni AR; Garai S; Thakur GA
    J Org Chem; 2017 Jan; 82(2):992-999. PubMed ID: 27966953
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal Chemistry.
    Ghosh AK; Brindisi M; Sarkar A
    ChemMedChem; 2018 Nov; 13(22):2351-2373. PubMed ID: 30187672
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partially modified retro-inverso peptides. Comparative Curtius rearrangements to prepare 1,1-diaminoalkane derivatives.
    Chorev M; Goodman M
    Int J Pept Protein Res; 1983 Mar; 21(3):258-68. PubMed ID: 6853027
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A facile stereoselective synthesis of alpha-glycosyl ureas.
    Bianchi A; Ferrario D; Bernardi A
    Carbohydr Res; 2006 Jul; 341(10):1438-46. PubMed ID: 16650393
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Organic azides: an exploding diversity of a unique class of compounds.
    Bräse S; Gil C; Knepper K; Zimmermann V
    Angew Chem Int Ed Engl; 2005 Aug; 44(33):5188-240. PubMed ID: 16100733
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DNA-templated functional group transformations enable sequence-programmed synthesis using small-molecule reagents.
    Sakurai K; Snyder TM; Liu DR
    J Am Chem Soc; 2005 Feb; 127(6):1660-1. PubMed ID: 15700999
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis and reactivity of 6,7-dihydrogeranylazides: reagents for primary azide incorporation into peptides and subsequent staudinger ligation.
    Xu J; Degraw AJ; Duckworth BP; Lenevich S; Tann CM; Jenson EC; Gruber SJ; Barany G; Distefano MD
    Chem Biol Drug Des; 2006 Aug; 68(2):85-96. PubMed ID: 16999773
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Palladium(II)-catalyzed rearrangement of glycal trichloroacetimidates: application to the stereoselective synthesis of glycosyl ureas.
    Mercer GJ; Yang J; McKay MJ; Nguyen HM
    J Am Chem Soc; 2008 Aug; 130(33):11210-8. PubMed ID: 18642810
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alpha,alpha-disubstituted glycines bearing a large hydrocarbon ring: peptide self-assembly through hydrophobic recognition.
    Ohwada T; Kojima D; Kiwada T; Futaki S; Sugiura Y; Yamaguchi K; Nishi Y; Kobayashi Y
    Chemistry; 2004 Feb; 10(3):617-26. PubMed ID: 14767925
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Synthesis fo asymmetric disubstituted urea and thiourea derivatives. 1].
    Drugărin C; Boldea A
    Pharmazie; 1976; 31(3):151-2. PubMed ID: 959263
    [No Abstract]   [Full Text] [Related]  

  • 19. Synthesis of N-trityl peptides by the Curtius azide method.
    ISELIN BM
    Arch Biochem Biophys; 1958 Dec; 78(2):532-8. PubMed ID: 13618035
    [No Abstract]   [Full Text] [Related]  

  • 20. Peptide-heterocycle hybrid molecules: solid-phase-supported synthesis of substituted N-terminal 5-aminotetrazole peptides via electrocyclization of peptidic imidoylazides.
    Gavrilyuk JI; Evindar G; Chen JY; Batey RA
    J Comb Chem; 2007; 9(4):644-51. PubMed ID: 17580974
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.