H. Steinhagen

发表

Preparation of chiral phosphorus, sulfur and selenium containing 2-aryloxazolines

M. Peer, J. D. Jong, M. Kiefer, 1996 .

Discovery and optimization of a new class of potent and non-chiral indole-3-carboxamide-based renin inhibitors.

Hans Matter, H. Matter, B. Scheiper, 2010, Bioorganic & medicinal chemistry letters.

Asymmetric Two‐Center Catalysis—Learning from Nature

H. Steinhagen, G. Helmchen, 1996 .

Drug delivery in oncology : from basic research to cancer therapy

F. Kratz, P. Senter, H. Steinhagen, 2011 .

Substituted uracil derivatives as potent inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1).

K. Schlemmer, H. Steinhagen, M. Gerisch, 2002, Bioorganic & medicinal chemistry letters.

A Convenient and Versatile Route to Hydroquinolines by Inter- and Intramolecular Aza-Diels-Alder Pathways.

E. Corey, H. Steinhagen, 1999, Angewandte Chemie.

Enantioselective catalysis with complexes of asymmetric P,N-chelate ligands

Günter Helmchen, P. Sennhenn, H. Steinhagen, 1997 .

(Eta3-phenylallyl)(phosphanyloxazoline)palladium complexes: X-ray crystallographic studies, NMR investigations, and Ab initio/DFT calculations.

M. Kollmar, S. Malinovskaya, F. Rominger, 2002, Chemistry.

Palladium‐Catalyzed Allylic Alkylation with Phosphinoaryldihydrooxazole Ligands: First Evidence and NMR Spectroscopic Structure Determination of a Primary Olefin–Pd0 Complex

H. Steinhagen, G. Helmchen, M. Reggelin, 1997 .

Asymmetric Allylic Substitutions with Palladium Complexes of Phosphinooxazolines as Ligands — Preparative and Mechanistic Aspects.

H. Steinhagen, G. Helmchen, M. Reggelin, 2002 .

A simple convergent approach to the synthesis of the antiviral agent virantmycin.

E. Corey, H. Steinhagen, 1999, Organic letters.

A simple convergent approach to the synthesis of the antiviral agent virantmycin.

E. Corey, H. Steinhagen, 1999, Organic letters.

Editorial: Channeling Drug Discovery

N. Damann, H. Steinhagen, 2012, ChemMedChem.

The Evolution of Drug Discovery: From Traditional Medicines to Modern Drugs. By Enrique Raviña.

H. Steinhagen, 2011 .

Structure of human G protein-coupled receptor kinase 2 in complex with the kinase inhibitor balanol.

D. Lodowski, V. Tesmer, J. Tesmer, 2010, Journal of medicinal chemistry.

Structure-based optimization of potent 4- and 6-azaindole-3-carboxamides as renin inhibitors.

Hans Matter, H. Matter, B. Scheiper, 2011, Bioorganic & medicinal chemistry letters.

Structure-based design and optimization of potent renin inhibitors on 5- or 7-azaindole-scaffolds.

Hans Matter, H. Matter, B. Scheiper, 2011, Bioorganic & medicinal chemistry letters.

Igniting Small‐Molecule Drug Discovery

H. Steinhagen, 2016, ChemMedChem.

Substituted Uracil Derivatives as Potent Inhibitors of Poly(ADP‐ribose)polymerase‐1 (PARP‐1)

K. Schlemmer, H. Steinhagen, M. Gerisch, 2003 .

Structure of human G protein-coupled receptor kinase 2 in complex with the kinase inhibitor balanol.

D. Lodowski, V. Tesmer, J. Tesmer, 2010, Journal of medicinal chemistry.