J. Stadlwieser

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Convenient Synthesis of 1H-Indol-1-yl Boronates via Palladium(0)-Catalyzed Borylation of Bromo-1H-indoles with `Pinacolborane'

J. Stadlwieser, Markus E. Dambaur, 2006 .

8-Fluoro-6-(methoxymethoxy)quinoline: Synthesis and regioselective functionalization via reaction with organolithium compounds

P. Barbier, Sven J. Taylor, J. Stadlwieser, 1998 .

[4-(imidazol-1-yl)thiazol-2-yl]phenylamines. A novel class of highly potent colchicine site binding tubulin inhibitors: synthesis and cytotoxic activity on selected human cancer cell lines.

T. Beckers, Mathias Schmidt, T. Maier, 2006, Journal of medicinal chemistry.

Combinatorial Solid-Phase Synthesis of Structurally Complex Thiazolylhydantoines.

W. Bannwarth, E. Ellmerer-Müller, J. Stadlwieser, 1998, Angewandte Chemie.

Novel Solution‐ and Solid‐Phase Strategies for the Parallel and Combinatorial Synthesis of Small‐Molecular‐Weight Compound Libraries

D. Obrecht, T. Masquelin, J. M. Villalgordo, 1997 .

8‐Fluoro‐6‐(methoxymethoxy)quinoline: Synthesis and Regioselective Functionalization via Reaction with Organolithium Compounds.

P. Barbier, Sven J. Taylor, J. Stadlwieser, 1998 .

Electrophilic N‐Amination of Imide Sodium Salts with O‐Diphenylphosphinylhydroxylamine (DPH): 7‐Aminotheophylline

J. Raneburger, W. Klötzer, J. Stadlwieser, 2003 .

1-Hydroxyimidazole Derivatives III.1,2 Synthesis of 1-Alkyloxy-, 1-Arylalkyloxy-, and 1-Phenoxy-1H-imidazoles

G. Laus, W. Klötzer, J. Stadlwieser, 1989 .

1-Hydroxyimidazole Derivatives. Part 3. Synthesis of 1-Alkyloxy-, 1-Arylalkyloxy-, and 1-Phenoxy-1H-imidazoles.

G. Laus, J. Stadlwieser, W. Kloetzer, 1990 .