A practical synthesis of 3-substituted Δ3,5(6)-Steroids as new potential 5α-reductase inhibitor

A practical synthesis of 3-substituted Δ3,5(6)-Steroids as new potential 5α-reductase inhibitor Synthesis of 4-trifluoromethylsteroids: A novel class of steroid 5α-reductase inhibitors Synthesis and biological evaluation of novel unsaturated carboxysteroids as human 5α-reductase inhibitors: A legitimate approach Synthesis and biological evaluation of 3-tetrazolo steroidal analogs: Novel class of 5α-reductase inhibitors Synthesis and Evaluation of 2‘-Substituted 4-(4‘-Carboxy- or 4‘-carboxymethylbenzylidene)-N-acylpiperidines: Highly Potent and in Vivo Active Steroid 5α-Reductase Type 2 Inhibitors Novel 17-Azolyl Steroids, Potent Inhibitors of Human Cytochrome 17α-Hydroxylase-C_17,20-lyase (P450₁₇_α):  Potential Agents for the Treatment of Prostate Cancer Synthesis and Evaluation of Novel Steroidal Oxime Inhibitors of P450 17 (17α-Hydroxylase/C17−20-Lyase) and 5α-Reductase Types 1 and 2 Synthesis of benzo[c]quinolizin-3-ones: Selective non-steroidal inhibitors of steroid 5α-reductase 1 Novel Steroidal Inhibitors of Human Cytochrome P45017.alpha.-Hydroxylase-C17,20-lyase): Potential Agents for the Treatment of Prostatic Cancer Synthesis and Evaluation of 17-Aliphatic Heterocycle-Substituted Steroidal Inhibitors of 17α-Hydroxylase/C17−20-Lyase (P450 17)