Issue 0, 1979

Total synthesis of 14α-hydroxyestrone 3-methyl ether

Abstract

Total synthesis of 14α-hydroxyestrone 3-methyl ether (5) was achieved by the thermolysis of 2-[2-(1,2-dihydro-4-methoxybenzocyclobuten-1-yl)ethyl] 3-hydroxy-2-methyl-3-vinylcyclopentan-1-one (27), obtained by Grignard reaction of 2-[2-(1,2-dihydro-4-methoxybenzocyclobuten-1-yl)ethyl]-2-methylcyclopentane-1,3-dione (26) with vinylmagnesium bromide. An alternative synthesis of (5) started from authentic 14-dehydroestradiol bis(t-butyldimethylsilyl) ether (28) and proceeded through estradiol-14α,15α-epoxide 3-methyl 17β-t-butyldimethylsilyl bisether (31).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 2830-2835

Total synthesis of 14α-hydroxyestrone 3-methyl ether

T. Kametani, H. Nemoto, M. Tsubuki, G. Purvaneckas, M. Aizawa and M. Nishiuchi, J. Chem. Soc., Perkin Trans. 1, 1979, 2830 DOI: 10.1039/P19790002830

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