Günther Ross

发表

Isoquinolin‐1‐one Inhibitors of the MDM2–p53 Interaction

Cédric Kalinski, Marcin Krajewski, Lutz Weber, 2008, ChemMedChem.

Stereoselective U-4CRS with 1-amino-5-desoxy-5-thio-2,3,4-O-isobutanoyl-β-d-xylopyranose: an effective and selectively removable chiral auxiliary

I. Ugi, E. Herdtweck, Günther Ross, 2002 .

Synthesis of substituted imidazolines by an Ugi/Staudinger/aza-Wittig sequence

L. Wessjohann, Jürgen Kolb, Cédric Kalinski, 2015 .

A new and versatile Ugi/SNAr synthesis of fused 4,5-dihydrotetrazolo[1,5-a]quinoxalines

Sébastien Gonnard, Cédric Kalinski, W. Hiller, 2006 .

Expeditious synthesis of imidazo[1,2-c]pyrimidines via a [4+1]-cycloaddition

C. Hulme, Hong Hu, Jürgen Kolb, 2007 .

On the industrial applications of MCRs: molecular diversity in drug discovery and generic drug synthesis

Lutz Weber, Cédric Kalinski, Michael Umkehrer, 2010, Molecular Diversity.

Tetramic acid derivatives via Ugi–Dieckmann-reaction

L. Allmendinger, Jürgen Kolb, Günther Ross, 2009 .

Multicomponent Reactions asa Powerful Tool for Generic Drug Synthesis

Cédric Kalinski, Michael Umkehrer, Christoph Burdack, 2008 .

Multicomponent Reactions as a Powerful Tool for Generic Drug Synthesis Multicomponent Reactions for Generic Drug Synthesis

Jurgen G Schmidt, Jürgen Kolb, Günther Ross, 2008 .

A facile synthesis of per-O-alkylated glycono-δ-lactones from per-O-alkylated glycopyranosides and a novel ring contraction for pyranoses

I. Ugi, H. Nothofer, Günther Ross, 1997 .