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Complex Polyfluoride Additives in Fmoc-Amino Acid Fluoride Coupling Processes. Enhanced Reactivity and Avoidance of Stereomutation

Authors :
Carpino, L. A.
Ionescu, D.
El-Faham, A.
Beyermann, M.
Henklein, P.
Hanay, C.
Wenschuh, H.
Bienert, M.
Source :
Organic Letters; April 2003, Vol. 5 Issue: 7 p975-977, 3p
Publication Year :
2003

Abstract

<UFIGR ID="ol020235an00001">Isolated Fmoc amino acid fluorides have previously been shown to be among the most efficient reagents for peptide bond formation. Now, it has been found that anionic, polyhydrogen fluoride additives are capable of diverting many of the classical peptide coupling processes to acid fluoride couplings. Examples include the use of N-HBTU or N-HATU and the carbodiimide technique. As HF-containing species, these additives provide a more suitable medium for the coupling of systems that are sensitive to loss of configuration at the reactive carboxyl function.

Details

Language :
English
ISSN :
15237060 and 15237052
Volume :
5
Issue :
7
Database :
Supplemental Index
Journal :
Organic Letters
Publication Type :
Periodical
Accession number :
ejs4444762