G. Dahmann

发表

A comparative cell-based high throughput screening strategy for the discovery of selective tyrosine kinase inhibitors with anticancer activity.

C. Stratowa, T. Metz, A. Baum, 1999, Anti-cancer drug design.

A simple synthesis of 4-(2-aminoethyl)-5-hydroxy-1H-pyrazoles

A. Meden, Uroš Grošelj, B. Stanovnik, 2007 .

Regioselective synthesis of 1- and 4-substituted 7-oxopyrazolo[1,5- a ]pyrimidine-3-carboxamides

Uroš Grošelj, B. Stanovnik, J. Svete, 2014 .

Getting a Grip on the Undrugged: Targeting β‐Catenin with Fragment‐Based Methods

Julian E. Fuchs, M. Pearson, D. Breitsprecher, 2020, ChemMedChem.

Hit to lead account of the discovery of bisbenzamide and related ureidobenzamide inhibitors of Rho kinase.

C. Cywin, E. Hickey, M. Kashem, 2010, Journal of medicinal chemistry.

Effective inhibitors of hemagglutination by influenza virus synthesized from polymers having active ester groups. Insight into mechanism of inhibition.

G M Whitesides, G. Whitesides, M. Mammen, 1995, Journal of medicinal chemistry.

Polyacrylamides Bearing Pendant α-Sialoside Groups Strongly Inhibit Agglutination of Erythrocytes by Influenza Virus: The Strong Inhibition Reflects Enhanced Binding through Cooperative Polyvalent Interactions

G. Whitesides, M. Mammen, G. Sigal, 1996 .

A Simple Synthesis of 5‐(2‐Aminophenyl)‐1H‐pyrazoles

Uroš Grošelj, B. Stanovnik, J. Svete, 2011 .

Discovery of Novel Spiro[3H-indole-3,2'-pyrrolidin]-2(1H)-one Compounds as Chemically Stable and Orally Active Inhibitors of the MDM2-p53 Interaction.

Markus J. Bauer, P. Ettmayer, D. Rudolph, 2016, Journal of medicinal chemistry.

Parallel synthesis of 7-heteroaryl-pyrazolo[1,5-a]pyrimidine-3-carboxamides

D. Kočar, Uroš Grošelj, B. Stanovnik, 2013, Molecular diversity.

Synthesis of 3D-Rich Heterocycles: Hexahydropyrazolo[1,5-a]pyridin-2(1H)-ones and Octahydro-2H-2a,2a1-diazacyclopenta[cd]inden-2-ones.

Uroš Grošelj, J. Svete, B. Štefane, 2016, The Journal of organic chemistry.

Diversity‐Oriented Synthesis of 2,5‐Disubstituted Tetrahydrofurans Based on a “Cyclization‐Hydrogenation‐Substitution” Strategy

P. Langer, G. Dahmann, Ilia Freifeld, 2006 .

One-pot parallel solution-phase synthesis of 1-substituted 4-(2-aminoethyl)-1H-pyrazol-5-ols.

A. Meden, Uroš Grošelj, A. Novak, 2008, Journal of combinatorial chemistry.

Stereoselective Synthesis of Alcohols, XLVI. Synthesis of a Hydroxytrioxaadamantane, a Model for the Trioxaadamantane Moiety of Muamvatin

R. W. Hoffmann, G. Dahmann, 1994 .

Stereoselective Synthesis of Alcohols, XXXVIII Stereoselective Total Synthesis of the Denticulatins

R. W. Hoffmann, G. Dahmann, M. Andersen, 1991 .

Parallel synthesis of 7-heteroaryl-pyrazolo[1,5-a]pyrimidine-3-carboxamides

D. Kočar, Uroš Grošelj, B. Stanovnik, 2013, Molecular Diversity.

Inhibition of Epidermal Growth Factor Receptor Activity by Two Pyrimidopyrimidine Derivatives

K. Heider, A. Baum, F. Solca, 2004, Journal of Pharmacology and Experimental Therapeutics.

Diversity-oriented synthesis of 1-substituted 4-aryl-6-oxo-1,6-dihydropyridine-3-carboxamides.

D. Kočar, Uroš Grošelj, B. Stanovnik, 2012, ACS combinatorial science.

Parallel Synthesis of 2-Substituted 6-(5-Oxo-1-phenylpyrrolidin-3-yl)pyrimidine-5-carboxamides

D. Kočar, Uroš Grošelj, B. Stanovnik, 2012, Molecules.

Parallel Synthesis of 1-Substituted5-(5-Oxopyrrolidin-3-yl)-1H-pyrazole-4-carboxamides

D. Kočar, Uroš Grošelj, A. Novak, 2011 .

A synthesis of 1-substituted 5-[2-(acylamino)ethyl]-1H-pyrazole-4-carboxamides

A. Meden, Uroš Grošelj, B. Stanovnik, 2009 .

Stereoselective Synthesis of Alcohols, XLV:1 Recent Developments in the Generation of the Stereotriad "D"

R. W. Hoffmann, G. Dahmann, M. Andersen, 1994 .

The absolute and relative configuration of muamvatin

R. W. Hoffmann, G. Dahmann, 1993 .

Synthesis of 1,5-disubstituted-4-oxo-4,5-dihydro-1H-pyrazolo[4,3-c]pyridine-7-carboxamides

Uroš Grošelj, B. Stanovnik, J. Svete, 2015 .

Synthesis of 2-substituted 6-(5-oxo-1-phenylpyrrolidin-3-yl)pyrimidin-4(3H)-ones

Uroš Grošelj, B. Stanovnik, J. Svete, 2013 .

Intracellular Trapping of the Selective Phosphoglycerate Dehydrogenase (PHGDH) Inhibitor BI-4924 Disrupts Serine Biosynthesis.

P. Ettmayer, W. Sommergruber, M. Pearson, 2019, Journal of medicinal chemistry.

Stereoselective Synthesis of Alcohols. Part 38. Stereoselective Total Synthesis of the Denticulatins.

R. W. Hoffmann, G. Dahmann, M. Andersen, 1991 .

Discovery of potent and selective PKC-θ inhibitors

Mario G. Cardozo, Mohammed A. Kashem, Carol Ann Homon, 2007 .

Discovery of potent and selective PKC-theta inhibitors.

Mohammed A Kashem, C. Homon, J. Woska, 2007, Bioorganic & medicinal chemistry letters.

Discovery of BI 7446: A Potent Cyclic Dinucleotide STING Agonist with Broad-Spectrum Variant Activity for the Treatment of Cancer.

S. Carotta, H. Nar, A. Grube, 2023, Journal of medicinal chemistry.