Synthesis of chiral 2-methyl-5,6,7,8-tetrahydroquinolines from naturally occurring monoterpenes
Articolo
Data di Pubblicazione:
2004
Citazione:
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.
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.
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.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Chiral tetrahydroquinolines; chiral pyridines; chiral nitrogen heterocycles; Kröhnke annulation
Elenco autori:
Orrù, Gianmauro; Soccolini, Francesco; Chelucci, Giorgio Adolfo
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