Optically active bicyclic dienes, 4 and 5 have been enantioselectively prepared in three and four steps, respectively. Mixtures of predominantly either the R or S enantiomer were obtained via an asymmetric alkylation of a chiral enamine.
|Original language||English (US)|
|Number of pages||6|
|State||Published - Feb 1 1995|
All Science Journal Classification (ASJC) codes
- Organic Chemistry