D. Barn

Optimisation of pharmacokinetic properties to afford an orally bioavailable and selective V1A receptor antagonist.

M. Craighead, Michael Kiczun, A. Lyons, 2011, Bioorganic & medicinal chemistry letters.

The discovery of novel 8-azabicyclo[3.2.1]octan-3-yl)-3-(4-chlorophenyl) propanamides as vasopressin V1A receptor antagonists.

F. Thomson, M. Craighead, G. Wishart, 2011, Bioorganic & medicinal chemistry letters.

Synthesis of an array of amides by aluminium chloride assisted cleavage of resin-bound esters

D. Rees, J. R. Morphy, D. Barn, 1996 .

Synthesis of novel analogues of the delta opioid ligand SNC-80 using AlCl3-promoted aminolysis.

A. Bom, J. R. Morphy, D. Barn, 1999, Bioorganic & medicinal chemistry letters.

Synthesis and SAR studies of 3-phenoxypropyl piperidine analogues as ORL1 (NOP) receptor agonists.

Mark A. Weston, R. Morphy, G. Wishart, 2005, Bioorganic & medicinal chemistry letters.

Design and synthesis of a maximally diverse and druglike screening library using REM resin methodology.

R. McGuire, Z. Rankovic, R. Dickins, 2001, Journal of combinatorial chemistry.

The discovery of novel indole-2-carboxamides as cannabinoid CB(1) receptor antagonists.

M. Deehan, G. Wishart, R. Goodwin, 2011, Bioorganic & medicinal chemistry letters.