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. Santaniello
Primo
;
P. Ferraboschi
Ultimo
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.
Settore BIO/10 - Biochimica
1981
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/182711
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