SYNTHESIS OF STEROIDS WITH NITROGEN-CONTAINING SUBSTITUENTS IN RING D
DOI:
https://doi.org/10.1007/902Keywords:
androstenone, pregnenolone, steroidsAbstract
Data published over the last 15 years on the chemical synthesis of biologically active steroids with nitrogen-containing substituents (mostly containing nitrogen heterocycles) in ring D are reviewed. Modern methods for the synthesis of nitrogen-containing derivatives from 17-keto steroids and 20-keto steroids and certain other methods for the synthesis of the target products are discussed. Concise data are also presented on three of the most important biological targets for nitrogen-containing steroids: enzymes 17α‑hydroxylase-17/20-lyase (CYP17), aromatase (CYP19), and 24-sterol methyltransferase (SMT).
Authors: S. V. Stulov and A. Yu. Misharin
English Translation in Chemistry of Heterocyclic Compounds, 2013, 48 (10), pp 1431-1472