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HBTU activation for automated Fmoc solid-phase peptide synthesis.

Authors :
Fields CG
Lloyd DH
Macdonald RL
Otteson KM
Noble RL
Source :
Peptide research [Pept Res] 1991 Mar-Apr; Vol. 4 (2), pp. 95-101.
Publication Year :
1991

Abstract

Excellent results have been obtained for the Fmoc solid-phase syntheses of peptides using the activating reagent 2-(1H-benzotriazol-1-yl)-1,1,3,3,-tetramethyluronium hexafluorophosphate (HBTU). Activation occurs very rapidly in N,N-dimethylformamide and N-methyl-pyrrolidone, optimal solvents for peptide-resin solvation. It has been observed that complete coupling reactions occur in only 10-30 min. Residues such as Arg, Ile, Leu and Val, which often require double coupling by other activation methods, react with high efficiency by single coupling when HBTU is used. The Fmoc/HBTU chemistry has recently been applied to the peptide synthesizers. The incorporation of trityl side-chain protection for Fmoc-Asn and Fmoc-Gln further enhances coupling efficiencies in difficult sequences.

Details

Language :
English
ISSN :
1040-5704
Volume :
4
Issue :
2
Database :
MEDLINE
Journal :
Peptide research
Publication Type :
Academic Journal
Accession number :
1815783