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Fmoc-L-Lys(Mtt)-OH
Chemischer Name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-epsilon-4-methyltrityl-L-lysine // Synonyme: Fmoc-Lys(Mtt)-OH
- Art-Nr.:FAA1135
- CAS Nr.:167393-62-6
- Lagertemperatur:2-8°C
- Formel:C41H40N2O4
- Molare Masse:624,8 g/mol
Ab 120,00 €
description
Building block with side protection orthogonal to Fmoc/tBu strategy. Can be used for side specific derivatization, for example for TFA mediated in situ cyclization, which is taking advantage of intermediate aspartamide formation.
references
A Tandem In Situ Peptide Cyclization through Trifluoroacetic Acid Cleavage; Koushik Chandra, Tapta Kanchan Roy, Deborah E. Shalev, Abraham Loyter, Chaim Gilon, R. Benny Gerber,
and Assaf Friedler; Angew. Chem. Int. Ed. 2014; 53: 9450-9455. DOI: 10.1002/anie.201402789.
Preparation of the very acid-sensitive Fmoc-Lys(Mtt)-OH. Application in the synthesis of side-chain to side-chain cyclic peptides and oligolysine cores suitable for the
solid-phase assembly of MAPs and TASPs; A. Aletras, K. Barlos, D. Gatos, S. Koutsogianni and P. Mamos; International journal of peptide and protein research 1995; 45: 488-96.
Synthesis of Modified Peptides; S. L. Mellor, D. A. Wellings, J.-A. Fehrentz, M. Paris, J. Martinez, N. J. Ede, A. M. Bray, D. J. Evans and G. B. Bloomberg; ChemInform 2000; 31:
no-no. doi:10.1002/chin.200043243
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