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Formation of 5-Aminomethyl-2,3-dihydropyridine-4(1<i>H</i>)-ones from 4-Amino-tetrahydropyridinylidene Salts

Various 4-aminotetrahydropyridinylidene salts were treated with aldehydes in an alkaline medium. Their conversion to 5-substituted β-hydroxyketones in a one-step reaction succeeded only with an aliphatic aldehyde. Instead, aromatic aldehydes gave 5-substituted β-aminoketones or a single δ-diketone....

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Autores principales: Werner Seebacher, Michael Hoffelner, Ferdinand Belaj, Teresa Pirker, Muaaz Alajlani, Rudolf Bauer, Eva-Maria Pferschy-Wenzig, Robert Saf, Robert Weis
Formato: Artigo
Lenguaje:Inglês
Publicado: MDPI AG 2023-09-01
Colección:Molecules
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Acceso en línea:https://www.mdpi.com/1420-3049/28/19/6869
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