J. Grutsch

发表

Synthesis of indolo[2,3-a]carbazole glycoside analogs of rebeccamycin: inhibitors of cyclin D1-CDK4

M. Faul, K. A. Sullivan, J. Grutsch, 2004 .

1,7-annulated indolocarbazoles as cyclin-dependent kinase inhibitors.

S. A. Watkins, C. D. Spencer, N. Stamm, 2004, Bioorganic & medicinal chemistry letters.

Synthesis, pharmacological characterization, and molecular modeling of heterobicyclic amino acids related to (+)-2-aminobicyclo[3.1.0] hexane-2,6-dicarboxylic acid (LY354740): identification of two new potent, selective, and systemically active agonists for group II metabotropic glutamate receptors.

J. Grutsch, D. Schoepp, J. Wepsiec, 1999, Journal of medicinal chemistry.

Synthetic approaches to indolo[6,7-a]pyrrolo[3,4-c]carbazoles: potent cyclin D1/CDK4 inhibitors.

S. W. Pedersen, M. Martinelli, J. M. Pawlak, 2004, The Journal of organic chemistry.

1,7-annulated indolocarbazoles as cyclin-dependent kinase inhibitors.

S. A. Watkins, C. D. Spencer, N. Stamm, 2004, Bioorganic & medicinal chemistry letters.

Reactions of [NiIII(cyclam)] with aqueous sulfur dioxide: Exhibition of a deuterium isotope effect and catalysis by chloride and bromide

J. Grutsch, D. E. Linn, Scott D. Rumage, 1993 .

Strategies for the synthesis of N-(azacycloalkyl)bisindolylmaleimides: selective inhibitors of PKCβ

Michael A. Staszak, M. Faul, K. A. Sullivan, 2003 .

Synthesis of 7-cyano- and 7-acetamido-indoles via cyanocarbonation/hydrogenation of 7-formyl indole

M. Faul, J. Grutsch, S. Kolis, 2003 .

Presence of Amino Acid Dehydrogenases and Transaminases in Myxococcus xanthus During Vegetative Growth and Myxospore Formation

J. Grutsch, D. White, M. Orlowski, 1974, Journal of bacteriology.

Synthesis of aryl- and heteroaryl[a]pyrrolo[3,4-c]carbazoles.

M. Faul, K. A. Sullivan, J. Grutsch, 2003, The Journal of organic chemistry.

Synthesis of Aryl‐ and Heteroaryl[a]pyrrolo[3,4‐c]carbazoles.

M. Faul, K. A. Sullivan, J. Grutsch, 2004 .