Boc-D-Lys(Aloc)-OH*DCHA

Nom chimique: N-alpha-t-Butyloxycarbonyl-N-epsilon-allyloxycarbonyl-D-lysine dicyclohexylamine // Synonymes: Boc-D-Lys(Alloc)-OH*DCHA

  • n° Art.:BAA1037
  • n° CAS:327156-94-5
  • Formule:C15H26N2O6*C12H23N
  • Storage temperature:2-8°C
  • Masse moléculaire:330,38*181,32 g/mol
  • Pureté:min. 98%
  • Pureté Énantiomérique:min. 99,7%

from 160,00 €

Grouped product items
Nombre Unité de vente Prix SKU Disponibilité
5 g
160,00 €
BAA1037.0005
sur demande
25 g
640,00 €
BAA1037.0025
sur demande
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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