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.
Regioselective mercuriation of an estradiol derivative: A facile entry to 2-substituted estrogens / E. Santaniello, P. Ferraboschi. - In: JOURNAL OF THE CHEMICAL SOCIETY, CHEMICAL COMMUNICATIONS. - ISSN 0022-4936. - :5(1981), pp. 217a-217a.
Regioselective mercuriation of an estradiol derivative: A facile entry to 2-substituted estrogens
E. SantanielloPrimo
;P. FerraboschiUltimo
1981
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.File in questo prodotto:
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