Abstract
An enantioselective approach to (+)-(S)-[n]-gingerols (1a-c) has been developed. The requisite stereogenic centers of target molecules are facilely constructed by the proline-catalyzed cross-aldol reaction from readily available achiral starting materials.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3909-3911 |
| Number of pages | 3 |
| Journal | Bioorganic and Medicinal Chemistry Letters |
| Volume | 19 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 15 2009 |
| Externally published | Yes |
Keywords
- Cross aldol
- Gingerols
- Organocatalysis
- Proline
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Pharmaceutical Science
- Drug Discovery
- Clinical Biochemistry
- Organic Chemistry