Abstract
A scalable synthesis of the neuroprotective agent P7C3-A20 is described. The synthesis has provided hundred-gram batches of the final compound for biological evaluation in rodents primates. The synthesis can be performed without chromatographic purification of intermediates or the final product.
Original language | English (US) |
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Pages (from-to) | 4429-4431 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 54 |
Issue number | 33 |
DOIs | |
State | Published - Aug 14 2013 |
Keywords
- Carbazole
- Fluorination
- Neuroprotective
- Synthesis
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry