M. Roberts

Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1.

Jennifer L. Harris, R. Epple, B. Bursulaya, 2005, Bioorganic & medicinal chemistry letters.

Synthesis of Reactive Poly(vinyl oxazolones) via Nitroxide-Mediated “Living” Free Radical Polymerization

R. B. Grubbs, B. Geierstanger, D. Tully, 2003 .

Synthesis and SAR of succinamide peptidomimetic inhibitors of cathepsin S.

Jennifer L. Harris, A. Chatterjee, R. Epple, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: heterocyclic P3.

Jun Li, Glen Spraggon, Tove Tuntland, 2006, Bioorganic & medicinal chemistry letters.

Discovery and biological evaluation of benzo[a]carbazole-based small molecule agonists of the thrombopoietin (Tpo) receptor.

J. Lao, A. Chatterjee, T. Tuntland, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and Chemistry of a Monotethered-POSS Bis(cyanate) Ester: Thermal Curing of Micellar Aggregates Leads to Discrete Nanoparticles

Brian J. Petteys, M. E. Wright, Gregory R. Yandek, 2007 .

Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based design.

H. M. Petrassi, Aaron Shipway, Jennifer L. Harris, 2008, Bioorganic & Medicinal Chemistry Letters.

Synthesis and SAR of arylaminoethyl amides as noncovalent inhibitors of cathepsin S: P3 cyclic ethers.

Jun Li, Glen Spraggon, Tove Tuntland, 2006, Bioorganic & medicinal chemistry letters.

Arylaminoethyl carbamates as a novel series of potent and selective cathepsin S inhibitors.

Jun Li, Tove Tuntland, Jennifer L. Harris, 2006, Bioorganic & medicinal chemistry letters.