Issue 3, 1989

Chiral construction of the estrane ring system by an intramolecular double Michael reaction

Abstract

Construction of the estrane ring system was achieved by the Intramolecular double Michael reaction as the key step. Heating of the α,β-unsaturated enone ester (18), prepared from the optically active indanone (4), with chlorotrimethylsilane, triethylamine, and zinc chloride produced three estrane derivatives (19), (22), and (25).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 529-535

Chiral construction of the estrane ring system by an intramolecular double Michael reaction

M. Ihara, T. Takahashi, N. Shimizu, Y. Ishida, I. Sudow, K. Fukumoto and T. Kametani, J. Chem. Soc., Perkin Trans. 1, 1989, 529 DOI: 10.1039/P19890000529

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