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.
2004
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.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/263692
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