M. O’Shea

Total synthesis of 6-deoxypladienolide D and Assessment of Splicing Inhibitory Activity in a Mutant SF3B1 cancer cell line.

M. Hao, M. Warmuth, Peter G. Smith, 2014, Organic letters.

Nonclinical pharmacokinetics and in vitro metabolism of H3B-6545, a novel selective ERα covalent antagonist (SERCA)

M. Warmuth, M. Korpal, Peter G. Smith, 2018, Cancer Chemotherapy and Pharmacology.

Biochemical and structural basis for the pharmacological inhibition of nuclear hormone receptor PPARγ by inverse agonists

M. Korpal, Lorna J. Mitchell, N. Larsen, 2022, The Journal of biological chemistry.

Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosides.

Jeremy R. Duvall, M. Foley, L. A. Marcaurelle, 2013, The Journal of organic chemistry.

Application of a catalytic asymmetric Povarov reaction using chiral ureas to the synthesis of a tetrahydroquinoline library.

L. A. Marcaurelle, Baudouin Gerard, S. Kesavan, 2012, ACS combinatorial science.

Discovery of Selective Estrogen Receptor Covalent Antagonists for the Treatment of ERαWT and ERαMUT Breast Cancer.

M. Hao, M. Warmuth, B. Caleb, 2018, Cancer discovery.

Abstract 3425: The discovery and characterization of CFT1946: A potent, selective, and orally bioavailable degrader of mutant BRAF for the treatment of BRAF-driven cancers

M. Sowa, L. Poling, Yanke Liang, 2023, Cancer Research.

Application of a catalytic asymmetric Povarov reaction using chiral ureas to the synthesis of a tetrahydroquinoline library.

Baudouin Gerard, S. Kesavan, E. Jacobsen, 2012, ACS combinatorial science.