Issue 8, 1993

Synthetic studies on the C/D ring segment of limonoids

Abstract

The diketone 3 has been synthesized from 4,7a-dimethyl-2,3,6,7-tetrahydroindene-1,5-dione 4. The furyl alcohol 7 has been dehydrated to give the cyclopentene 9 and the resulting epoxide 10 and the diol 11 have been converted into the diketone 3. Attempted Baeyer–Villiger oxidation of the dione 3 failed to give the expected lactone 2.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1993, 995-998

Synthetic studies on the C/D ring segment of limonoids

M. Renoud-Grappin, C. Vanucci and G. Lhommet, J. Chem. Soc., Perkin Trans. 1, 1993, 995 DOI: 10.1039/P19930000995

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