Estrogens can be regiospecifically functionalized at the position 2 by a few electrophilic reagents. Reactions of estradiol 3-methyl ether-17 beta-acetate with Hg(OAc)2 and BF3 . Et2O/Ac2O allows the preparation of 2-chloromercurio- and 2-organoboron-derivatives respectively. Both the above compounds are useful starting material for easy preparations of 2-catecholestrogens and 2-chloromercurio-derivative can be transformed in other functionalized estrogens. New procedures for the preparation of 2,4-dinitroestrone and 2-nitroestrone are also described.

New routes to A-ring substituted estrogens / E. Santaniello, P. Ferraboschi. - In: JOURNAL OF STEROID BIOCHEMISTRY. - ISSN 0022-4731. - 19:1 Part 3(1983), pp. 767-769.

New routes to A-ring substituted estrogens

E. Santaniello
Primo
;
P. Ferraboschi
Ultimo
1983

Abstract

Estrogens can be regiospecifically functionalized at the position 2 by a few electrophilic reagents. Reactions of estradiol 3-methyl ether-17 beta-acetate with Hg(OAc)2 and BF3 . Et2O/Ac2O allows the preparation of 2-chloromercurio- and 2-organoboron-derivatives respectively. Both the above compounds are useful starting material for easy preparations of 2-catecholestrogens and 2-chloromercurio-derivative can be transformed in other functionalized estrogens. New procedures for the preparation of 2,4-dinitroestrone and 2-nitroestrone are also described.
Settore BIO/10 - Biochimica
1983
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/181793
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