115303-33-8Relevant academic research and scientific papers
SYNTHESIS OF NEW ANTIATHEROMATOUS DRUGS. STUDY OF THE ESTERIFICATION OF 17β-HYDROXY-5α-ANDROSTAN-3-ONE
Volovel'skii, L. N.,Koryukina, V. N.,Popova, N. V.,Rastrepina, I. A.,Borozenets, L. K.
, p. 444 - 446 (2007/10/02)
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.
