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Fmoc-L-Lys(ivDde)-OH
Nombre químico: N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-epsilon-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine // Sinónimos: N-alpha-Fmoc-N-epsilon-ivDde-L-lysine, Fmoc-Lys(ivDde)-OH
- Nº Artículo:FAA1500
- Nº CAS:204777-78-6
- Fórmula:C34H42N2O6
- Storage temperature:2-8°C
- Masa molecular:574,72 g/mol
- Pureza:min. 98%
- Pureza Enantiomérica:min. 99,9%
from 56,00 €
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. BennyGerber, and Assaf Friedler; Angew. Chem. Int. Ed. 2014; 53: 9450-9455. DOI: 10.1002/anie.201402789.
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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