B. v. Kerékjártó

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

Pharmacy, Medicinal Chemistry, Pharmacology +12

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

Pharmacy, Medicinal Chemistry, Pharmacology +11

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 3. Lactones of 6-phenoxy-3,5-dihydroxyhexanoic acids

Heiner Jendralla, E. Granzer, B. v. Kerékjártó et al. · Journal of Medicinal Chemistry · 1991 · 51 citations · Full text

Life Sciences, Biochemistry, Pharmacology +10

Convenient two-step stereospecific hydroxy-substitution with retention in β-hydroxy-δ-lactones. 4 ()-heterosubstituted mevinolin and -analogs

Wilhelm Bartmann, G. Beck, E. Granzer et al. · Tetrahedron Letters · 1986 · 24 citations

Pharmacy, Chemistry, Medicinal Chemistry +7

Synthesis of a novel HMG-COA reductase inhibitor

E. Baader, Wilhelm Bartmann, G. Beck et al. · Tetrahedron Letters · 1988 · 16 citations

Pharmacy, Medicinal Chemistry, Pharmacology +6