SYNTHESIS OF NEW ANTIATHEROMATOUS DRUGS. STUDY OF THE ESTERIFICATION OF 17β-HYDROXY-5α-ANDROSTAN-3-ONE

DOI: 10.1007/BF00575703

Source and publish data:

Chemistry of Natural Compounds p. 444 - 446 (1983)

Update date:2022-08-05

Topics:

Authors:

Volovel'skii, L. N.

Koryukina, V. N.

Popova, N. V.

Rastrepina, I. A.

Borozenets, L. K.

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Article abstract of DOI:10.1007/BF00575703

The acylation of dihydrotestosterone with propionyl and p-chlorophenoxyisobutyryl chlorides leads to the formation of dihydrotestosterone esters and the 3-enol acylates of the dihydrotestosterone esters.The acid hydrolysis of the 3-enol acylates converts them into the coresponding dihydrotestosterone esters.

Full text of DOI:10.1007/BF00575703

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