Abstract
The bromination of chiral crystalline samples of 4,4′-dimethylchalcone was reinvestigated. In the presence of the optically active reaction product, (+)- or (-)-chalcone dibromide, crystallization from solutions of the achiral chalcone is specifically directed toward one-handedness. A feedback mechanism can thus be envisaged where optically active compounds are formed, generate additional material of the same chirality, and communicate this chirality to other regions, simply by cycles of solidification, reaction, and liquefaction.
Keywords
Affiliated Institutions
Related Publications
Trifluoroacetamides from Amino Alcohols as Nucleophilic Trifluoromethylating Reagents
Both non-enolizable and enolizable carbonyl compounds underwent nucleophilic trifluoromethylation by a new family of cheap and efficient trifluoroacetamide reagents derived from...
Publication Info
- Year
- 1974
- Type
- article
- Volume
- 185
- Issue
- 4150
- Pages
- 525-527
- Citations
- 46
- Access
- Closed
External Links
Social Impact
Social media, news, blog, policy document mentions
Citation Metrics
Cite This
Identifiers
- DOI
- 10.1126/science.185.4150.525
- PMID
- 17830404