Heiner Jendralla

Vanadium(<scp>II</scp>)‐ and Niobium(<scp>III</scp>)‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to <i>C</i>₂‐Symmetrical HIV‐Protease Inhibitors

Bernhard Kammermeier, Gerhard Beck, Heiner Jendralla et al. · Angewandte Chemie International Edition in English · 1994 · 74 citations

Combinatorial Chemistry, Molecular Biology, Organic Chemistry +18

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 1. Lactones of pyridine- and pyrimidine-substituted 3,5-dihydroxy-6-heptenoic (-heptanoic) acids

G. Beck, E. Baader, Wilhelm Bartmann et al. · Journal of Medicinal Chemistry · 1990 · 68 citations · Full text

Practical Large Scale Synthesis of tert-Butyl (3R,5S)-6-Hydroxy-3,5-O-isopropylidene-3,5-dihydroxyhexanoate: Essential Building Block for HMG-CoA Reductase Inhibitors

Gerhard Beck, Heiner Jendralla · Synthesis · 1995 · 68 citations

Medicinal Chemistry, Hmg-coa Reductase Inhibitors, Biochemistry +15

Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor

Günther Wess, E. Baader, Wilhelm Bartmann et al. · Tetrahedron Letters · 1990 · 65 citations

Medicinal Chemistry, Biochemistry, Medicine +8

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 2. Derivatives of 7-(1H-pyrrol-3-yl)-substituted-3,5-dihydroxyhept-6(E)-enoic (-heptanoic) acids

Heiner Jendralla, E. Baader, Wilhelm Bartmann et al. · Journal of Medicinal Chemistry · 1990 · 64 citations · Full text