Jacques Cercus

Diasterio‐ und enantioselektive Reduktion von β‐Ketoestern mit Cyclopentanon‐, Cyclohexanon‐, Piperidon‐ und Tetralon‐Struktur durch nicht fermentierende Bäcker‐Hefe

Dieter Seebàch, Silvio Roggo, Thomas Maetzke et al. · Helvetica Chimica Acta · 1987 · 99 citations

Engineering, Biochemistry, Biotechnology +12

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 4:  Preparation of Fragment C₇_-₂₄

Stuart J. Mickel, Gottfried Sedelmeier, Daniel Niederer et al. · Organic Process Research & Development · 2003 · 86 citations

Natural Sciences, Chemistry, Medicinal Chemistry +15

The development of a practical synthesis of the potent and selective somatostatin sst3 receptor antagonist [4-(3,4-difluoro-phenyl)-piperazine-1-yl]-{(4S,4aS,8aR)-2[(S)-3-(6-methoxy-pyridin-3-yl)-2-methyl-propyl]-decahydroisoquinoline-4-yl}-methanone (NVP-ACQ090)

Markus Bänziger, Jacques Cercus, Hans Hirt et al. · Tetrahedron Asymmetry · 2003 · 28 citations

Pharmacy, Medicinal Chemistry, Pharmacology +13

A Formal Synthesis of (+)-Discodermolide

Olivier Loiseleur, Guido Koch, Jacques Cercus et al. · Organic Process Research & Development · 2005 · 25 citations

Natural Sciences, Chemistry, Medicinal Chemistry +13

Synthesis of new N-aryl oxindoles as intermediates for pharmacologically active compounds

Murat Acemoglu, Thomas Allmendinger, John Calienni et al. · Tetrahedron · 2004 · 20 citations

Pharmacy, Medicinal Chemistry, Pharmacology +7