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Boc-L-4,4-DfNva-OH
Nom chimique: (S)-2-t-Butyloxycarbonylamino-4,4-difluoropentanoic acid // Synonymes: Boc-L-DfpGly-OH, Boc-(2,2-difluoroprop-1-yl)-L-glycine, Boc-L-4,4-F2Nva-OH, (S)-2-((tert-butoxycarbonyl)amino)-4,4-difluoropentanoic acid, Boc-4,4-DfNva-OH
- n° Art.:BAA4380
- n° CAS:208521-08-8
- Formule:C10H17F2NO4
- Masse moléculaire:253,25 g/mol
from Sur demande
references
Towards identifying preferred interaction partners of fluorinated amino acids within the hydrophobic environment of a dimeric coiled coil peptide; T. Vagt, E. Nyakatura, M. Salwiczek, C. Jackel and B. Koksch; Org Biomol Chem 2010; 8: 1382-6. https://doi.org/10.1039/b917205j
Position-dependent effects of fluorinated amino acids on the hydrophobic core formation of a heterodimeric coiled coil; M. Salwiczek, S. Samsonov, T. Vagt, E. Nyakatura, E. Fleige, J. Numata, H. Colfen, M. T. Pisabarro and B. Koksch; Chemistry 2009; 15: 7628-36. https://doi.org/10.1002/chem.200802136
Effects of fluorination on the folding kinetics of a heterodimeric coiled coil; M. Salwiczek and B. Koksch; Chembiochem : a European journal of chemical biology 2009; 10: 2867-70. https://doi.org/10.1002/cbic.200900518
Fluorine in a native protein environment--How the spatial demand and polarity of fluoroalkyl groups affect protein folding; C. Jackel, M. Salwiczek and B. Koksch; Angew Chem Int Ed Engl 2006; 45: 4198-203. https://doi.org/10.1002/anie.200504387
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