C. Huwe

发表

Identification of orally bioavailable, non-amidine inhibitors of Urokinase Plasminogen Activator (uPA).

M. Adler, M. Whitlow, R. Pulk, 2009, Bioorganic & medicinal chemistry letters.

A Flexible Synthesis of Azasugars and Homoazasugars via Olefin Metathesis

S. Blechert, C. Huwe, S. Blechert*, 1997 .

Design, synthesis and biological evaluation of aryl-substituted sialyl Lewis X mimetics prepared via cross-metathesis of C-fucopeptides.

T. Woltering, J. Jiricek, C. Wong, 1999, Bioorganic & medicinal chemistry.

A novel, thioacetal based linker for solid-phase synthesis

C. Huwe, H. Künzer, 1999 .

One pot synthesis of N-derivatized 2-oxazolidinones from amino alcohol carbamates

S. Blechert, C. Huwe, 1994 .

A novel approach to azasugars from vinyl glycine methyl ester via olefin metathesis

S. Blechert, C. Huwe, 1995 .

Synthesis of nitrogen heterocycles from vinyl glycine derivatives via palladium catalysis

S. Blechert, C. Huwe, 1994 .

A CATALYST-SPECIFIC, STEREOCONTROLLED RING-CLOSING METATHESIS

S. Blechert, C. Huwe, J. Velder, 1996 .

Structural insights into species-specific features of the ribosome from the human pathogen Mycobacterium tuberculosis

J. Sacchettini, J. Jakana, Jeng-Yih Chang, 2017, Nucleic acids research.

Discovery of quinolines as selective glucocorticoid receptor agonists.

Markus Berger, Werner Skuballa, Stefan Jaroch, 2010, Bioorganic & medicinal chemistry letters.

Synthetic library design.

Christoph M Huwe, C. Huwe, 2006, Drug discovery today.

The importance of chemistry for the future of the pharma industry.

Hanno Wild, H. Wild, C. Huwe, 2011, Angewandte Chemie.