GENERAL METHODS FOR THE SYNTHESIS OF STYRYLPYRIDINIUM SALTS

Authors

Keywords:

styrylpyridinium salts, fluorophores, Knoevenagel condensation, Aldol condensation, Wittig reaction, Horner-Wadsworth-Emmons reaction

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 4pyridinecarboxaldehyde 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.

 

Author Biographies

Reinis Putralis, Latvian Institute of Organic Synthesis

Latvian Institute of Organic Synthesis,
21 Aizkraukles St., Riga LV-1006, Latvia; е-mail: reinis.putralis@osi.lv

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Riga Stradiņš University,
21 Konsula St., Riga LV-1007, Latvia

 

 

Aiva Plotniece, Latvian Institute of Organic Synthesis

Latvian Institute of Organic Synthesis,
21 Aizkraukles St., Riga LV-1006, Latvia;

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Riga Stradiņš University,
21 Konsula St., Riga LV-1007, Latvia

 

Kārlis Pajuste, Latvian Institute of Organic Synthesis

Latvian Institute of Organic Synthesis,
21 Aizkraukles St., Riga LV-1006, Latvia

Published

2024-12-13

Issue

Section

Heterocycles in Focus