Abstract
An efficient route to a key intermediate in the synthesis of lavendamycin from a suitably substituted 2-chloroquino-line derivative via aminocarbonylation with tryptophan methyl ester as nucleophile, is reported.
Original language | English |
---|---|
Pages (from-to) | 22-24 |
Number of pages | 3 |
Journal | Journal of Chemical Research - Part S |
Issue number | 1 |
DOIs | |
Publication status | Published - 2002 |
Keywords
- Aminocarbonylation
- Lavendamycin
- Palladium catalysis
- Quinolines
- Tryptophan
ASJC Scopus subject areas
- General Chemistry