Emergence of single-molecular chirality from achiral reactants

73Citations
Citations of this article
85Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The synthesis of enantiopure molecules from achiral precursors without the need for pre-existing chirality is a major challenge associated with the origin of life. We here show that an enantiopure product can be obtained from achiral starting materials in a single organic reaction. An essential characteristic of this reaction is that the chiral product precipitates from the solution, introducing a crystal-solution interface which functions as an asymmetric autocatalytic system that provides sufficient chiral amplification to reach an enantiopure end state. This approach not only provides more insight into the origin of life but also offers a pathway to acquire enantiopure compounds for industrial applications.

Cite

CITATION STYLE

APA

Steendam, R. R. E., Verkade, J. M. M., Van Benthem, T. J. B., Meekes, H., Van Enckevort, W. J. P., Raap, J., … Vlieg, E. (2014). Emergence of single-molecular chirality from achiral reactants. Nature Communications, 5. https://doi.org/10.1038/ncomms6543

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free