Abstract
N-(4-Arylazobenzoyl)-1H-benzotriazoles 15a, 15b react with dipeptides 12a-d, (12d+12d′) and tripeptides 14a, 14b to give azodye labeled-dipeptides (16a-e), (16d+16d′), (16e+16e′) and -tripeptides 16f, 16g in high yields (73-93%) with retention of chirality.
Original language | English (US) |
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Pages (from-to) | 611-617 |
Number of pages | 7 |
Journal | Chemical Biology and Drug Design |
Volume | 73 |
Issue number | 6 |
DOIs | |
State | Published - Jun 2009 |
Externally published | Yes |
Keywords
- Azodye
- Benzotriazole methodology
- N-protected(α-aminoacyl) benzotriazole
- Photoisomerization
- Small peptides