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HBTU activation for automated Fmoc solid-phase peptide synthesis.
- 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