The synthesis is reported of chiral substituted 2-methylpyridines, in which the pyridine rings are annulated at the 5,6-positions to the chiral frameworks originating from (-)-β-pinene, (-)-isopinocampheol and (+)-camphor. Two procedures have been evaluated for their preparation.
Synthesis of chiral 2-methyl-5,6,7,8-tetrahydroquinolines from naturally occurring monoterpenes / Orrù, Gianmauro; Soccolini, Francesco; Chelucci, Giorgio Adolfo. - 2004:xiv(2004), pp. 44-50.
Synthesis of chiral 2-methyl-5,6,7,8-tetrahydroquinolines from naturally occurring monoterpenes
Soccolini, Francesco;Chelucci, Giorgio Adolfo
2004-01-01
Abstract
The synthesis is reported of chiral substituted 2-methylpyridines, in which the pyridine rings are annulated at the 5,6-positions to the chiral frameworks originating from (-)-β-pinene, (-)-isopinocampheol and (+)-camphor. Two procedures have been evaluated for their preparation.File in questo prodotto:
| File | Dimensione | Formato | |
|---|---|---|---|
|
Chelucci_G_Articolo_2004_Synthesis.pdf
accesso aperto
Tipologia:
Versione editoriale (versione finale pubblicata)
Licenza:
Non specificato
Dimensione
113.4 kB
Formato
Adobe PDF
|
113.4 kB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
