C. Mularski

Discovery of zoniporide: a potent and selective sodium-hydrogen exchanger type 1 (NHE-1) inhibitor with high aqueous solubility.

R. J. Hill, D. Knight, A. Guzman-Perez, 2001, Bioorganic & medicinal chemistry letters.

Utility of p-nitrophenyl 3-bromo-2,2-diethoxypropionate (NPBDP) in heterocyclic synthesis

John L. LaMattina, Christian J. Mularski, J. Lamattina, 1984 .

Synthesis of 2-amino-5-hydroxy-4-pyrimidones and 5,6-biheteroaryls using p-nitrophenyl 3-bromo-2,2-diethoxypropionate (NPBDP)

J. Lamattina, C. Mularski, D. E. Muse, 1988 .

Isozyme-nonselective N-Substituted Bipiperidylcarboxamide Acetyl-CoA Carboxylase Inhibitors Reduce Tissue Malonyl-CoA Concentrations, Inhibit Fatty Acid Synthesis, and Increase Fatty Acid Oxidation in Cultured Cells and in Experimental Animals*

D. Hargrove, D. Dalvie, J. Chapman, 2003, Journal of Biological Chemistry.

.alpha.-Hydroxy thioamides: useful intermediates for the synthesis of functionalized thiazoles

J. Lamattina, C. Mularski, 1986 .

Dihydropyridines: A New Class of Angiotensin II Antagonists.

K. W. Hoover, M. Mangiapane, M. Burkard, 1994 .

The reaction of 5-acetyl-2-aminooxazole with amines: an approach to 1H-5-acetyl-2-aminoimidazoles

J. Lamattina, C. Mularski, 1984 .