Chemometric sensing of stereoisomeric compound mixtures with a redox-responsive optical probe.


Journal

Chemical science
ISSN: 2041-6520
Titre abrégé: Chem Sci
Pays: England
ID NLM: 101545951

Informations de publication

Date de publication:
24 Jan 2024
Historique:
received: 25 10 2023
accepted: 20 12 2023
medline: 26 1 2024
pubmed: 26 1 2024
entrez: 26 1 2024
Statut: epublish

Résumé

The analysis of mixtures of chiral compounds is a common task in academic and industrial laboratories typically achieved by laborious and time-consuming physical separation of the individual stereoisomers to allow interference-free quantification, for example using chiral chromatography coupled with UV detection. Current practice thus impedes high-throughput and slows down progress in countless chiral compound development projects. Here we describe a chemometric solution to this problem using a redox-responsive naphthoquinone that enables chromatography-free click chemistry sensing of challenging mixtures. The achiral probe covalently binds amino alcohols within a few minutes at room temperature and generates characteristic UV

Identifiants

pubmed: 38274061
doi: 10.1039/d3sc05706b
pii: d3sc05706b
pmc: PMC10806675
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1498-1504

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

The authors declare no competing conflicts.

Auteurs

Jeffrey S S K Formen (JSSK)

Department of Chemistry, Georgetown University Washington DC 20057 USA cw27@georgetown.edu.

Diandra S Hassan (DS)

Department of Chemistry, Georgetown University Washington DC 20057 USA cw27@georgetown.edu.

Christian Wolf (C)

Department of Chemistry, Georgetown University Washington DC 20057 USA cw27@georgetown.edu.

Classifications MeSH