Alkoxyalkylation of Electron-Rich Aromatic Compounds

Alkoxyalkylation and hydroxyalkylation methods utilizing oxo-compound derivatives such as aldehydes, acetals or acetylenes and various alcohols or water are widely used tools in preparative organic chemistry to synthesize bioactive compounds, biosensors, supramolecular compounds and petrochemicals....

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Simon Péter
Lőrinczi Bálint
Szatmári István
Dokumentumtípus: Cikk
Megjelent: 2024
Sorozat:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 25 No. 13
Tárgyszavak:
doi:10.3390/ijms25136966

mtmt:35074742
Online Access:http://publicatio.bibl.u-szeged.hu/33697
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520 3 |a Alkoxyalkylation and hydroxyalkylation methods utilizing oxo-compound derivatives such as aldehydes, acetals or acetylenes and various alcohols or water are widely used tools in preparative organic chemistry to synthesize bioactive compounds, biosensors, supramolecular compounds and petrochemicals. The syntheses of such molecules of broad relevance are facilitated by acid, base or heterogenous catalysis. However, degradation of the N-analogous Mannich bases are reported to yield alkoxyalkyl derivatives via the retro-Mannich reaction. The mutual derivative of all mentioned species are quinone methides, which are reported to form under both alkoxy- and aminoalkylative conditions and via the degradation of the Mannich-products. The aim of this review is to summarize the alkoxyalkylation (most commonly alkoxymethylation) of electron-rich arenes sorted by the methods of alkoxyalkylation (direct or via retro-Mannich reaction) and the substrate arenes, such as phenolic and derived carbocycles, heterocycles and the widely examined indole derivatives. 
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856 4 0 |u http://publicatio.bibl.u-szeged.hu/33697/1/IntJMolSci_6966_Simon_2024.pdf  |z Dokumentum-elérés