Fmoc-L-Ser[Psi(Me,Me)Pro]-OH

Nom chimique: (S)-3-(N-alpha-(9-Fluorenylmethyloxycarbonyl)-2,2-dimethyloxyzolidine-4-carboxylic acid // Synonymes: (S)-3-(((9H-fluoren-9-yl)methoxy)carbonyl)-2,2-dimethyloxazolidine-4-carboxylic acid, Fmoc-Ser[Psi(Me,Me)Pro]-OH

  • n° Art.:FAA8590
  • n° CAS:1201651-31-1
  • Formule:C21H21NO5
  • Storage temperature:2-8°C
  • Masse moléculaire:367,40 g/mol
  • Pureté:min. 98%
  • Pureté Énantiomérique:min. 99,7%

from 125,00 €

Grouped product items
Nombre Unité de vente Prix SKU Disponibilité
5 g
125,00 €
FAA8590.0005
<10 jour ouvrables
25 g
500,00 €
FAA8590.0025
<10 jour ouvrables
100 g
1 500,00 €
FAA8590.0100
<10 jour ouvrables
Fiches de données de sécurité
description

This building block is a pseudoproline monomer for SPPS. It can be successfully coupled with various amino acids using modern coupling techniques avoiding the need for pseudoproline dipeptides and giving the possibility to introduce pseudoprolines in peptides containing non-natural or rare amino acids. For coupling efficiency studies please see Senko et al, 2021.


references

Scope and limitations of pseudoprolines as individual amino acids in peptide synthesis; D. A. Senko, N. D. Timofeev, I. E. Kasheverov, I. A. Ivanov; Amino Acids 2021; 53: 665-671. https://doi.org/10.1007/s00726-021-02973-1


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/ja962780a

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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