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

Author:

Ahmed M. Giasuddin1,Moeiz Syed M. Iqbal1,Ahmed S. Asghari1,Kiuchi Fumiyuki2,Tsuda Yoshisuke3,Sampson Paul4

Affiliation:

1. Department of Chemistry, University of Dhaka, Dhaka 1000, Bangladesh

2. Department of Pharmacognosy, Graduate School of Pharmaceutical science, Kyoto University, Yoshida, Sakyo-Ku, Kyoto 606-8501, Japan

3. Faculty of Pharmaceutical sciences, Kanazawa University, 13-1 Takara-Machi, Kanazawa 920, Japan

4. Department of Chemistry, Kent State University, USA

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.

Publisher

SAGE Publications

Subject

General Chemistry

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