Chemistry of Natural Compounds

, Volume 19, Issue 4, pp 444–446 | Cite as

Synthesis of new antiatheromatous drugs. Study of the esterification of 17β-hydroxy-5α-androstan-3-one

  • L. N. Volovel'skii
  • V. N. Koryukina
  • N. V. Popova
  • I. A. Rastrepina
  • L. K. Borozenets
Article
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Abstract

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 corresponding dihydrotestosterone esters.

Keywords

Anhydrous Sodium Sulfate Sodium Chloride Solution Dihydrotestosterone Propionyl Testosterone Propionate 

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Copyright information

© Plenum Publishing Corporation 1984

Authors and Affiliations

  • L. N. Volovel'skii
  • V. N. Koryukina
  • N. V. Popova
  • I. A. Rastrepina
  • L. K. Borozenets

There are no affiliations available

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