H. Paulsen

发表

Dysregulation of bacterial proteolytic machinery by a new class of antibiotics

H. Sahl, J. Bandow, C. Ladel, 2005, Nature Medicine.

Corrigendum: Dysregulation of bacterial proteolytic machinery by a new class of antibiotics

H. Sahl, J. Bandow, C. Ladel, 2005, Nature Medicine.

Medicinal Chemistry Optimization of Acyldepsipeptides of the Enopeptin Class Antibiotics

T. Lampe, H. Labischinski, H. Brötz-Oesterhelt, 2006, ChemMedChem.

Design and Synthesis of Potent and Selective Azaindole‐Based Rho Kinase (ROCK) Inhibitors

J. Stasch, M. Radtke, H. Ehmke, 2008, ChemMedChem.

Efficient regioselective synthesis of 6-amino-5-benzoyl-1-substituted 2(1H)-pyridinones.

A. Göller, J. Benet‐Buchholz, H. Paulsen, 2005, The Journal of organic chemistry.

p38 kinase inhibitors for the treatment of arthritis and osteoporosis: thienyl, furyl, and pyrrolyl ureas.

J. S. Johnson, S. Wilhelm, W. Scott, 2001, Bioorganic & Medicinal Chemistry Letters.

Synthesis of the insect pheromone (+)-eldanoline by enantioselective homoaldol reaction

H. Paulsen, D. Hoppe, 1992 .

CONVENIENT SYNTHESIS OF ENANTIOMERICALLY ENRICHED (OXYBUTENYL)STANNANES AND THEIR LEWIS ACID CATALYZED HOMOALDOL REACTIONS

H. Paulsen, D. Hoppe, C. Graeve, 1996 .

Scalable Synthesis of the Desoxy-biphenomycin B Core

T. Lampe, S. Raddatz, H. Paulsen, 2011 .

Discovery of BAY 94‐8862: A Nonsteroidal Antagonist of the Mineralocorticoid Receptor for the Treatment of Cardiorenal Diseases

Alexander Hillisch, Joachim Mittendorf, A. Hillisch, 2012, ChemMedChem.

Structures of ClpP in complex with acyldepsipeptide antibiotics reveal its activation mechanism

H. Song, H. Brötz-Oesterhelt, H. Paulsen, 2010, Nature Structural &Molecular Biology.

Synthesis and pharmacological characterization of a potent, orally active p38 kinase inhibitor.

S. Wilhelm, W. Scott, J. Pirro, 2002, Bioorganic & medicinal chemistry letters.

Improved Synthesis of the Selective Rho-Kinase Inhibitor 6-Chloro-N4-{3,5-difluoro-4-[(3-methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]phenyl}pyrimidin-2,4-diamine

Ping Gao, H. Paulsen, H. Schirok, 2010 .

New Generation of sGC Stimulators: Discovery of Imidazo[1,2-a]pyridine Carboxamide BAY 1165747 (BAY-747), a Long-Acting Soluble Guanylate Cyclase Stimulator for the Treatment of Resistant Hypertension.

H. Trübel, J. Stasch, M. Follmann, 2023, Journal of medicinal chemistry.

Chromanol derivatives--a novel class of CETP inhibitors.

H. Paulsen, Olaf Weber, H. Bischoff, 2011, Bioorganic & medicinal chemistry letters.