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Fmoc-L-Leu-L-Thr[PSI(Me,Me)Pro]-OH
Nom chimique: (4S,5R)-3-(N-(9-Fluorenylmethyloxycarbonyl)-L-leucinyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid // Synonymes: Fmoc-Leu-Thr[PSI(Me,Me)Pro]-OH
- n° Art.:PSI1210
- n° CAS:955048-89-2
- Formule:C28H34N2O6
- Storage temperature:2-8°C
- Masse moléculaire:494,58 g/mol
from 65,00 €
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/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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Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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