Abstract
A very simple and cheap linker has been used for solid-phase synthesis of peptide aldehydes. Protected amino acid aldehydes are immobilized on 2-Cl(trt) resin as oxazolidine formation via diethanolamine. After classical Fmoc SPPS, treatment of the resin with AcOH/DCM/H 2O (8:1:1) affords peptide aldehydes in high yield and purity.
Original language | English |
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Pages (from-to) | 1187-1188 |
Number of pages | 2 |
Journal | Bioorganic and Medicinal Chemistry Letters |
Volume | 22 |
Issue number | 2 |
DOIs | |
State | Published - 15 Jan 2012 |
Keywords
- 2-Cl(trt) resin
- Diethanolamine
- Oxazolidine
- Peptide aldehydes
- Solid-phase synthesis