Abstract
A highly diastereoselective methodology for the efficient synthesis of functionalized indolo[2,3-a]quinolizidine skeletons in a one-pot operation has been developed. The protocol makes use of simple and inexpensive starting materials such as tryptamines, 1,3-dicarbonyl compounds and α,β- unsaturated aldehydes in the presence of a Brønsted acid catalyst.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 79-82 |
| Number of pages | 4 |
| Journal | RSC ADVANCES |
| Volume | 1 |
| Issue number | 1 |
| DOIs | |
| State | Published - Aug 7 2011 |
| Externally published | Yes |
ASJC Scopus subject areas
- General Chemistry
- General Chemical Engineering