✍ Scribed by Thomas Hitz; Pier Luigi Luisi
No coin nor oath required. For personal study only.
This article is concerned with the chiral amplification of oligopeptides formed in the polymerization of chiral, nonracemic mixtures of the N‐carboxyanhydride (NCA) of Leu and Glu in aqueous solution. Labeling (deuteration) of one enantiomer and reversed‐phase and normal‐phase high‐performance liquid chromatography mass spectrometry (RP‐ and NP‐HPLC/MS, respectively) were used to determine the product distribution, both with respect to oligopeptide chain length and stereoisomer distribution. Starting the polymerization with an enantiomeric excess (ee) of 20% of the L‐enantiomer (L‐amino acid/D‐amino acid 6 : 4) leads to an ee of 73% at the level of the homochiral enantiomeric (Leu)~5~, and of 71% at the level of the homochiral enantiomeric (Glu)~7~. For the Leu system and in the presence of a solid support (quartz), the ee reached values of up to 100%. We argue that such amplification processes could be relevant for the chemical evolution towards single‐handedness.
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