Issue 5, 1981

Regioselective mercuriation of an estradiol derivative: a facile entry to 2-substituted estrogens

Abstract

3-Methoxy-17β-acetoxy-1,3,5(10)-estratriene was regioselectively chloromercuriated at C-2 to afford (1d), which was converted into the 2-bromo- and 2-iododerivatives.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 217a-217a

Regioselective mercuriation of an estradiol derivative: a facile entry to 2-substituted estrogens

E. Santanello and P. Ferraboschi, J. Chem. Soc., Chem. Commun., 1981, 217a DOI: 10.1039/C3981000217A

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