Issue 5, 1999

Synthesis of Some Substituted Adamantane-2,4-diones from 4,4-Disubstituted Cyclohexanone Enamines and α,β-Unsaturated Acid Chlorides

Abstract

Following our previous report7 on the synthesis of adamantane derivatives by condensation of 4,4-disubstituted cyclohexanone enamines with α,β-unsaturated acid chlorides, we now report the synthesis of seven new substituted adamantanediones from the reactions of three cyclohexanone enamines (4, Y=phenyl, isopropenyl, methyl) in which one of the substituents is an acetyl group.

Article information

Article type
Paper

J. Chem. Res. (S), 1999, 316-317

Synthesis of Some Substituted Adamantane-2,4-diones from 4,4-Disubstituted Cyclohexanone Enamines and α,β-Unsaturated Acid Chlorides

M. Giasuddin Ahmed, S. M. Iqbal Moeiz, S. Asghari Ahmed, F. Kiuchi, Y. Tsuda and P. Sampson, J. Chem. Res. (S), 1999, 316 DOI: 10.1039/A900581A

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