Fmoc-L-Lys(Boc)-L-Thr[PSI(Me,Me)Pro]-OH

Chemical name: (4S,5R)-3-(N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-epsilon-t-butyloxycarbonyl-L-lysinyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid // Synonyms: Fmoc-Lys(Boc)-Thr[PSI(Me,Me)Pro]-OH

  • Product code:PSI1200
  • CAS No.:911838-56-7
  • Formula:C33H43N3O8
  • Storage temperature:2-8°C
  • Molecular weight:609.71 g/mol

from $93.75

Grouped product items
Qty Packing unit Price SKU Availability
1 g
$93.75
PSI1200.0001
<10 business days
5 g
$293.75
PSI1200.0005
<10 business days
25 g
$1,093.75
PSI1200.0025
<10 business days
Safety Data Sheets
description

Pseudoprolines derived from Serine and Threonine have developed to standard building blocks for peptide synthesis since their invention.


references

Pseudo-Prolines as a Molecular Hinge:  Reversible Induction of cis Amide Bonds into Peptide Backbones; P. Dumy, M. Keller, D. E. Ryan, B. Rohwedder, T. Wöhr and M. Mutter; J. Am. Chem. Soc. 1997; 119: 918-925. https://doi.org/10.1021/ja962780


Pseudo-Prolines as a Solubilizing, Structure-Disrupting Protection Technique in Peptide Synthesis; T. Wöhr, F. Wahl, A. Nefzi, B. Rohwedder, T. Sato, X. Sun and M. Mutter; J. Am. Chem. Soc. 1996; 118: 9218-9227. https://doi.org/10.1021/ja961509q


Expediting the Fmoc solid phase synthesis of long peptides through the application of dimethyloxazolidine dipeptides; P. White, J. W. Keyte, K. Bailey and G. Bloomberg; J. Pept. Sci. 2004; 10: 18-26. https://doi.org/10.1002/psc.484


Pseudoprolines as Removable Turn Inducers: Tools for the Cyclization of Small Peptides; D. Skropeta, K. A. Jolliffe, and P. Turner; J. Org. Chem. 2004; 69: 8804-8809. https://doi.org/10.1021/jo0484732

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