Abstract
Facile and efficient synthetic routes for fluorogenic anilides of L-arginine have been developed. The amide bond formation uses phosphorous oxychloride as a condensing agent. The synthesis is simple, rapid, and affords excellent yields.
Original language | English (US) |
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Pages (from-to) | 3465-3471 |
Number of pages | 7 |
Journal | Synthetic Communications |
Volume | 34 |
Issue number | 19 |
DOIs | |
State | Published - 2004 |
Externally published | Yes |
Keywords
- 2-Aminobenzoic acid
- Fluorogenic substrates
- Synthesis
- Trypsin
ASJC Scopus subject areas
- Organic Chemistry