C. Li

Synthesis and biological activity of a potent and orally bioavailable SCD inhibitor (MF-438).

J. Falgueyret, R. Oballa, J. Guay, 2010, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of 5,6-diarylimidazo[2.1-b]thiazole as selective COX-2 inhibitors

D. Riendeau, P. Prasit, C. Brideau, 1997 .

Synthesis of (±)-3-Amino-2-(4-chlorophenyl)propanesulfonic acid (Saclofen)

R. Dolle, W. Howson, C. Li, 1991 .

Characterization of the in vitro oxidative metabolites of the COX-2 selective inhibitor L-766,112

J. Yergey, C. Li, L. Trimble, 1997 .

Cobalt-mediated cyclization of amino acid derivatives. Application to the kainoids

J. Baldwin, C. Li, 1987 .

Enantiospecific synthesis of acromelic acid A via a cobalt-mediated cyclisation reaction

J. Baldwin, Chunju Li, C. Li, 1988 .

Enhancement of mass spectrometric detection of LTC4, LTD4, and LTE4 by derivatization

J. Yergey, O. Mamer, G. Just, 1994, Journal of the American Society for Mass Spectrometry.

Enantioselective synthesis of (+)-pinidine

R. Dolle, Chunju Li, K. I. Osifo, 1991 .