A. Judkins

Design and synthesis of aryl ether and sulfone hydroxamic acids as potent histone deacetylase (HDAC) inhibitors.

D. Kitchen, Chittari Pabba, B. T. Gregg, 2011, Bioorganic & medicinal chemistry letters.

A novel highly stereoselective synthesis of 2,3-disubstituted 3H-quinazoline-4-one derivatives.

A. Judkins, J. Treiberg, E. Kesicki, 2007, Organic letters.