Heinrich Estermann

Industrial Synthesis of the Key Precursor in the Synthesis of the Anti-Influenza Drug Oseltamivir Phosphate (Ro 64-0796/002, GS-4104-02):  Ethyl (3<i>R</i>,4<i>S</i>,5<i>S</i>)-4,5-epoxy-3-(1-ethyl-propoxy)-cyclohex-1-ene-1-carboxylate

Muriel Federspiel, R. Fischer, Michael Hennig et al. · Organic Process Research & Development · 1999 · 155 citations

Pharmacy, Chemistry, Medicinal Chemistry +8

Diastereoselektive Alkylierung von 3‐Aminobutansäure in der 2‐Stellung

Heinrich Estermann, Dieter Seebàch · Helvetica Chimica Acta · 1988 · 130 citations

Natural Sciences, Biochemistry, Chemistry +14

The Synthetic-Technical Development of Oseltamivir Phosphate Tamiflu™: A Race against Time

Stefan Abrecht, René Trussardi, Gösta Rimmler et al. · CHIMIA International Journal for Chemistry · 2007 · 68 citations · Full text

Pharmacy, Medicinal Chemistry, Pharmacology +14

α-Alkylation of β-aminobutanoates with lk-1.2-induction

Dieter Seebàch, Heinrich Estermann · Tetrahedron Letters · 1987 · 67 citations

Life Sciences, Biochemistry, Medicinal Chemistry +3

Large scale preparation of chiral building blocks for the P3 site of renin inhibitors

Stephan Doswald, Heinrich Estermann, Ernst Kupfer et al. · Bioorganic & Medicinal Chemistry · 1994 · 50 citations

Pharmacy, Medicinal Chemistry, Pharmacology +13