Peter Droescher

Novel “scavestrogens” and their radical scavenging effects, iron-chelating, and total antioxidative activities: Δ8,9-dehydro derivatives of 17α-estradiol and 17β-estradiol

Wolfgang Römer, M. Öettel, Peter Droescher et al. · Steroids · 1997 · 60 citations

Bioorganic Chemistry, Food Bioactive Compound, Biochemistry +9

Novel estrogens and their radical scavenging effects, iron-chelating, and total antioxidative activities: 17α-substituted analogs of Δ9(11)-dehydro-17β-estradiol

Wolfgang Römer, M. Öettel, Bernd Menzenbach et al. · Steroids · 1997 · 57 citations

Novel Estrogens, Biochemistry, Radical Scavenging Effects +8

Structure-based design, synthesis and in vitro characterization of potent 17β-hydroxysteroid dehydrogenase type 1 inhibitors based on 2-substitutions of estrone and D-homo-estrone

Gabriele Möller, Dominga Deluca, Christian Gege et al. · Bioorganic & Medicinal Chemistry Letters · 2009 · 45 citations · Full text

Vitro Characterization, Medicinal Chemistry, Biochemistry +8

A nickelacycle as propionic acid equivalent for carbon-carbon coupling reactions; application to the synthesis of C25 steroid carboxylic acids

Bruno Schönecker, Dirk Walther, Reinald Fischer et al. · Tetrahedron Letters · 1990 · 44 citations

Cross-coupling Reaction, Carboxylic Acids, Engineering +10

An Improved Synthesis of (24<i>R</i>)-24,25-Dihydroxyprovitamin D₃ ¹

E Schrötter, Bruno Schönecker, Ulrich Hauschild et al. · Synthesis · 1990 · 18 citations

Diversity Oriented Synthesis, Pharmaceutical Chemistry, Bioorganic Chemistry +14