Jo Van Betsbrugge

New amino acids derived from L-pyroglutamic acid: Synthesis of Trans-4-benzyl-cis-5-phenyl-L-proline, L-α-(2-benzyl-3-phenylpropyl)-glycine and L-α-(3-phenylpropyl)-glycine

Jo Van Betsbrugge, Wim Van Den Nest, Patricia Verheyden et al. · Tetrahedron · 1998 · 24 citations

New Amino Acids, Biosynthesis, Engineering +6

A convenient synthesis of protected (R)-α-phenylproline derivatives using the Mitsunobu reaction

Jo Van Betsbrugge, Dirk Tourwé, Bernard Kaptein et al. · Tetrahedron · 1997 · 23 citations

Derivative (Chemistry), Derivatives, Mitsunobu Reaction +8

A Novel Linking-Protecting Group Strategy for Solid-Phase Organic Chemistry with Configurationally Stable α-[<i>N</i>-(Phenylfluorenyl)]amino Carbonyl Compounds:  Synthesis of Enantiopure Norephedrines on Solid Support

Francis Gosselin, Jo Van Betsbrugge, Mostafa Hatam et al. · The Journal of Organic Chemistry · 1999 · 20 citations

Asymmetric Catalysis, Cross-coupling Reaction, Enantioselective Synthesis +14

HPLC Separation of Enantiomers of α‐Substituted Proline Analogues by the Application of (<i>S</i>)‐<i>N</i>‐(4‐Nitrophenoxy‐carbonyl)phenylalanine Methoxyethyl Ester as Chiral Derivatizing Agent

Antal Péter, G. Török, Erika Vékes et al. · Journal of Liquid Chromatography & Related Technologies · 2004 · 10 citations

Chiral Derivatizing Agent, Biochemistry, Medicine +14