Abstract
The chemistry of firefly bioluminescence is important for numerous applications in biochemistry and analytical chemistry. The emitter of this bioluminescent system, firefly oxyluciferin, is difficult to handle. The cause of its lability was clarified while its synthesis was reinvestigated. A side product was identified and characterized by NMR spectroscopy and X-ray crystallography. The reason for the lability of oxyluciferin is now ascribed to autodimerization of the coexisting enol and keto forms in a Mannich-type reaction. Light into the darkness: Firefly oxyluciferin, the emitter of firefly bioluminescence, is notoriously difficult to handle. The cause behind its chemical lability is now ascribed to autodimerization of the coexisting enol (showing blue fluorescence in DMSO) and keto forms (contributing to the green fluorescence in water) in a Mannich reaction.
Original language | English (US) |
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Pages (from-to) | 847-850 |
Number of pages | 4 |
Journal | Angewandte Chemie - International Edition |
Volume | 53 |
Issue number | 3 |
DOIs | |
State | Published - Jan 13 2014 |
Keywords
- bioorganic chemistry
- heterocycles
- luminescence
- natural products
- structure elucidation
ASJC Scopus subject areas
- Catalysis
- General Chemistry