Joseph Foricher

New developments in enantioselective hydrogenation

R. Schmid, Emil A. Broger, Marco Cereghetti et al. · Pure and Applied Chemistry · 1996 · 287 citations · Full text

Enantioselective Synthesis, Engineering, Catalysis +4

Axially Dissymmetric Diphosphines in the Biphenyl Series: Synthesis of (6,6′‐Dimethoxybiphenyl‐2,2′‐diyl)bis(diphenylphosphine)(‘MeO‐BIPHEP’) and Analogues <i>via</i> an <i>ortho</i>‐Lithiation/Iodination <i>Ullmann</i>‐Reaction Approach

Rudolf Schmid, Joseph Foricher, Marco Cereghetti et al. · Helvetica Chimica Acta · 1991 · 261 citations

Dissymmetric Diphosphines, Natural Sciences, Diversity-oriented Synthesis +12

Practical synthesis of (S)-2-(4-fluorophenyl)-3-methylbutanoic acid, key building block for the calcium antagonist Mibefradil

Yvo Crameri, Joseph Foricher, Michelangelo Scalone et al. · Tetrahedron Asymmetry · 1997 · 36 citations

Calcium Antagonist Mibefradil, Practical Synthesis, Key Building Block +6

Development of a Scalable Synthesis of (<i>S</i>)-3-Fluoromethyl-γ-butyrolactone, Building Block for Carmegliptin’s Lactam Moiety

Jean‐Michel Adam, Joseph Foricher, Steven P. Hanlon et al. · Organic Process Research & Development · 2011 · 36 citations

Engineering, Several New Routes, Desired Lactone +17

Photoreaktionen des 3‐Methyl‐4‐phenylsydnons

Karl‐Heinz Pfoertner, Joseph Foricher · Helvetica Chimica Acta · 1980 · 27 citations

Engineering, Photoredox Process, Photochemistry +9