C. Michoud

发表

Synthesis and activity of quinolinyl-methylene-thiazolinones as potent and selective cyclin-dependent kinase 1 inhibitors.

L. Vassilev, Qing Xiang, C. Tovar, 2007, Bioorganic & medicinal chemistry letters.

Benzazepinones and benzoxazepinones as antagonists of inhibitor of apoptosis proteins (IAPs) selective for the second baculovirus IAP repeat (BIR2) domain.

Robert T. Taylor, A. Polonskaia, M. Weisel, 2013, Journal of medicinal chemistry.

Optimization of benzodiazepinones as selective inhibitors of the X-linked inhibitor of apoptosis protein (XIAP) second baculovirus IAP repeat (BIR2) domain.

A. Polonskaia, M. Weisel, C. Lukacs, 2013, Journal of medicinal chemistry.

A general solution to the synthesis of 2-azabicyclo[3.3.1]nonane unit of Strychnos alkaloids

C. Michoud, V. Rawal, 1991 .

General strategy for the stereocontrolled synthesis of Strychnos alkaloids: a concise synthesis of (.+-.)-dehydrotubifoline

C. Michoud, V. Rawal, R. Monestel, 1993 .

Scope of alkoxymethyl radical cyclizations

C. Michoud, C. Dufour, V. Rawal, 1993 .

An unexpected Heck reaction. Inversion of olefin geometry facilitated by the apparent intramolecular carbamate chelation of the .sigma.-palladium intermediate

C. Michoud, V. Rawal, 1993 .

Cyclization of alkoxymethyl radicals

C. Michoud, C. Dufour, V. Rawal, 1991 .

Development of amino-pyrimidine inhibitors of c-Jun N-terminal kinase (JNK): kinase profiling guided optimization of a 1,2,3-benzotriazole lead.

Johannes C. Hermann, C. Lukacs, A. Kuglstatter, 2013, Bioorganic & medicinal chemistry letters.

Expression, characterization and structure determination of an active site mutant (Glu202-Gln) of mini-stromelysin-1.

O. El-Kabbani, J. Birktoft, J. Engler, 2000, Protein engineering.