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Abstract
This microreview covers the general methods on the synthesis of mono-, bis-, and tristyrylpyridinium fluorophores described in the literature in recent years. A summary of the most common synthesis can be divided into four distinct methods: aldol condensation followed by N-alkylation of pyridine moiety, Knoevenagel condensation reaction of picolinium salt and aldehyde, Wittig reaction of triphenylphosphine salt and pyridine aldehyde followed by N-alkylation of pyridine moiety, and Horner reaction between bisphosphonate derivative and 4-pyridinecarboxaldehyde followed by N-alkylation of pyridine moiety. Metal-catalyzed reactions were not reviewed. The microreview primary focuses on the synthesis of styrylpyridinium salts having in their structures a 4-pyridinium moiety.
| Original language | English |
|---|---|
| Article number | 117377 |
| Pages (from-to) | 439-441 |
| Journal | Chemistry of Heterocyclic Compounds |
| Volume | 60 |
| Issue number | 9/10 |
| DOIs | |
| Publication status | Published - Sept 2024 |
Field of Science*
- 1.4 Chemical sciences
- 3.1 Basic medicine
Publication Type*
- 1.1. Scientific article indexed in Web of Science and/or Scopus database
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The synthesis, properties, and applications of styrilpyridine derivatives with conjugated double-bond systems
Putrālis, R. (Project leader), Plotniece, A. (Supervisor) & Pajuste, K. (Supervisor)
2/10/23 → 30/09/27
Project: PhD projects