Fluorescent α-amino acids


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
30 Aug 2023
Historique:
medline: 15 8 2023
pubmed: 15 8 2023
entrez: 15 8 2023
Statut: epublish

Résumé

The Heck-Matsuda coupling reaction of arenediazonium salts derived from L-phenylalanine with various alkenes has been developed. A two-step process involving the preparation of a tetrafluoroborate diazonium salt from a 4-aminophenylalanine derivative, followed by a palladium(0)-catalysed Heck-Matsuda coupling reaction allowed access to a range of unnatural α-amino acids with cinnamate, vinylsulfone and stilbene side-chains. Analysis of the photophysical properties of these unnatural α-amino acids demonstrated that the (

Identifiants

pubmed: 37580965
doi: 10.1039/d3ob01096a
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6932-6939

Auteurs

Rochelle McGrory (R)

School of Chemistry, University of Glasgow, The Joseph Black Building, Glasgow, G12 8QQ, UK. Andrew.Sutherland@glasgow.ac.uk.

Rebecca Clarke (R)

School of Chemistry, University of Glasgow, The Joseph Black Building, Glasgow, G12 8QQ, UK. Andrew.Sutherland@glasgow.ac.uk.

Olivia Marshall (O)

School of Chemistry, University of Glasgow, The Joseph Black Building, Glasgow, G12 8QQ, UK. Andrew.Sutherland@glasgow.ac.uk.

Andrew Sutherland (A)

School of Chemistry, University of Glasgow, The Joseph Black Building, Glasgow, G12 8QQ, UK. Andrew.Sutherland@glasgow.ac.uk.

Classifications MeSH