V. Teetz

Synthesis of unnatural amino acids: (S,S,S)-2-azabicyclo[3.3.0]octane-3-carboxylic acid

V. Teetz, Rolf Geiger, H. Gaul · Tetrahedron Letters · 1984 · 44 citations

Bioorganic Chemistry, Engineering, Unnatural Amino Acids +4

Syntheses of 4(R)-silyloxy-6(S)-iodomethyl-tetrahydropyran-2-one and its enantiomer, building blocks for HMG-COA reductase inhibitors

E. Baader, Wilhelm Bartmann, G. Beck et al. · Tetrahedron Letters · 1988 · 26 citations

Building Blocks, Medicinal Chemistry, Hmg-coa Reductase Inhibitors +8

Synthesis of a highly active angiotensin converting enzyme inhibitor: 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498).

V. Teetz, Rolf Geiger, Rolf Henning et al. · PubMed · 1984 · 23 citations

Improved Bioavailability, Pharmacotherapy, Heterocycle Chemistry +16

Analogues and fragments of secretin

Wolfgang König, Martin Bickel, Karl Karch et al. · Peptides · 1984 · 13 citations

Protein Secretion, Biochemistry, Natural Sciences +7

Alkaloid biosynthesis in Croton flavens L

K. L. Stuart, V. Teetz, B. Franck · Journal of the Chemical Society D Chemical Communications · 1969 · 11 citations

V. Teetz, Biosynthesis, B. Franck +10