The synthesis of 2-alkyl-3-aryl-substituted quinuclidines was accomplished in a simple synthetic sequence. The separation of enantiomers was carried out using chiral HPLC. (C) 2000 Elsevier Science Ltd.
|Original language||English (US)|
|Number of pages||4|
|Publication status||Published - Dec 16 2000|
ASJC Scopus subject areas
- Organic Chemistry
- Drug Discovery