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

AutocatalysisMechanism (biology)Abiotic componentOptically activeChemistryAutocatalytic reactionBiophysicsBiochemical engineeringAstrobiologyChemical physicsPhysicsEcologyOrganic chemistryBiologyCatalysisStatistical physicsEngineering

Affiliated Institutions

Related Publications

Publication Info

Year
1974
Type
article
Volume
185
Issue
4150
Pages
525-527
Citations
46
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

46
OpenAlex
0
Influential
42
CrossRef

Cite This

Bernard S. Green, Lilly Heller (1974). Mechanism for the Autocatalytic Formation of Optically Active Compounds under Abiotic Conditions. Science , 185 (4150) , 525-527. https://doi.org/10.1126/science.185.4150.525

Identifiers

DOI
10.1126/science.185.4150.525
PMID
17830404

Data Quality

Data completeness: 77%