Issue 0, 1966

Studies on sesquiterpenoids. Part XIV. Total synthesis of (±)-atractylon

Abstract

The structure of a furanosesquiterpene, atractylon, isolated from Atractylis ovata Thunb and Atractylodes japonica Koizumi, was established by Yosioka and his co-workers. As starting material for the synthesis of atractylon, 2,3,4,6,7,8-hexahydro-2-oxonaphthalene has been used, and 4,4a,5,6,7,8,8a,9-octahydro-3,8a-dimethyl-5-methylenenaphtho[2,3-b] furan has been synthesised. This racemic compound is identical with atractylon, by comparison of infrared spectra.

Article information

Article type
Paper

J. Chem. Soc. C, 1966, 1866-1872

Studies on sesquiterpenoids. Part XIV. Total synthesis of (±)-atractylon

H. Minato and T. Nagasaki, J. Chem. Soc. C, 1966, 1866 DOI: 10.1039/J39660001866

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