Chiroptical Sensing of Amines With Isatins

Isatins are extensively researched compounds with diverse applications, particularly as synthetic precursors in pharmaceutical developments. However, their use as optical probes for enantioselective sensing of chiral amines has not been explored to date. Herein, we present a novel chiroptical assay with an optimized isatin that generates strong, red-shifted circular dichroism (CD) signals at approximately 380 nm upon ketimine formation with chiral amines. The intensity of the induced CD signal increases linearly with the enantiomeric excess of the analyte and thus allows quantitative chirality analysis. The general usefulness of this approach is demonstrated with a broad range of aliphatic and aromatic chiral amines, and by accurate determination of the enantiomeric composition of 10 samples.

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Publication Details

Journal
Chirality
Published
2024-10-24
DOI
https://doi.org/10.1002/chir.70002
Citations
4
Primary Topic
Molecular spectroscopy and chirality
Type
article
Field-Weighted Citation Impact
0.96

Funders

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article

Chiroptical Sensing of Amines With Isatins

Christian Wolf, Samantha L. Pilicer, F. Safia Kariapper, Flavia Miccolis
4 citations
Chirality
Molecular spectroscopy and chirality
0.96
article

Chiroptical Sensing of Amines With Isatins

Christian Wolf, Samantha L. Pilicer, F. Safia Kariapper, Flavia Miccolis
article en
4 citations

Abstract

Isatins are extensively researched compounds with diverse applications, particularly as synthetic precursors in pharmaceutical developments. However, their use as optical probes for enantioselective sensing of chiral amines has not been explored to date. Herein, we present a novel chiroptical assay with an optimized isatin that generates strong, red-shifted circular dichroism (CD) signals at approximately 380 nm upon ketimine formation with chiral amines. The intensity of the induced CD signal increases linearly with the enantiomeric excess of the analyte and thus allows quantitative chirality analysis. The general usefulness of this approach is demonstrated with a broad range of aliphatic and aromatic chiral amines, and by accurate determination of the enantiomeric composition of 10 samples.

ChiralityVol. 36(11)
Georgetown University (US)
National Science Foundation, National Institute of General Medical Sciences
Openalex Percentile: Top 27%
Molecular spectroscopy and chirality
0.96
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