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Fmoc-L-Lys(iNoc)-OH
Chemischer Name: N-alpha-(9-Fluorenylmethoxycarbonyl)-N-epsilon-pyridylmethoxycarbonyl-L-lysine, Fmoc-L-Lys(isonicotinyloxycarbonyl)-OH // Synonyme: Fmoc-Lys(iNoc)-OH
- Art-Nr.:FAA8775
- CAS Nr.:1459694-90-6
- Lagertemperatur:2-8°C
- Formel:C28H29N3O6
- Molare Masse:503,56 g/mol
- Reinheit:min. 98%
- Enantiomerenreinheit:min. 99,7%
Ab 108,00 €
description
This orthogonally side-chain protected Lysine is stable to most reagents used in peptide synthesis. The isonicotinyloxycarbonyl (iNoc)-group can be removed under mild reducing conditions like Zn/AcOH, Pd/C/H2, SmI2 in aq. DMF etc. Isomeric purity >99.9%.
references
Isonicotinyloxycarbonyl a novel amino protecting group for peptide synthesis; D. F. Veber, W. J. Paleveda, Y. C. Lee, R. Hirschmann; J. Org. Chem. 1977; 42(20): 3286-3288. https://doi.org/10.1021/jo00440a018.
Total Synthesis and Structural Characterization of Caveolin-1; H. Hojo, T. Takei, Y. Asahina, N. Okumura, T. Takao, M. So, I. Suetake, T. Sato, A. Kawamoto, Y. Hirabayashi; Angew. Chem. Int. Ed. 2021; 60(25): 13900-13905. https://doi.org/10.1002/anie.202100826.
Chemoenzymatic Synthesis of the Immunoglobulin Domain of Tim-3 Carrying a Complex-Type N-Glycan by Using a One-pot Ligation; Y. Asahina, S. Kamitori, T. Takao, N. Nishi, H. Hojo; Angew. Chem. Int. Ed. 52(37): 9733-9737. https://doi.org/10.1002/anie.201303073.
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