A. Pimm

1,2-Dihydro-4-quinazolinamines: potent, highly selective inhibitors of inducible nitric oxide synthase which show antiinflammatory activity in vivo.

A. Tinker, H. Beaton, N. Boughton-Smith, 2003, Journal of medicinal chemistry.

Palladium-Catalysed Intramolecular Cyclisations of Olefinic Propargylic Carbonates and application to the diastereoselective synthesis of enantiomerically pure (−)-α-thujone

A. Pimm, W. Oppolzer, B. Stammen, 1997 .

The Preparation and Pd(0)-Catalysed Cross Coupling Reactions of α-(Phenylthio)alkenylzinc Reagents

A. Pimm, P. Kocieňski, S. Street, 1992 .

A Synthesis of Jaspamide Based on 1,2-Metallate Rearrangements of α-Heteroalkenylmetal Derivatives

P. Jankowski, A. Pimm, P. Kocieňski, 1995 .

Palladium-Catalyzed Intramolecular Cyclization of Olefinic Propargylic Carbonates and Application to the Diastereoselective Synthesis of Enantiomerically Pure (-)-α-Thujone.

W. E. Hume, A. Pimm, W. Oppolzer, 1997 .

The discovery of novel, potent and highly selective inhibitors of inducible nitric oxide synthase (iNOS).

Glen Andrews, Paul D Leeson, Anders Åberg, 2011, Bioorganic & medicinal chemistry letters.

Discovery of potent and selective adamantane-based small-molecule P2X(7) receptor antagonists/interleukin-1beta inhibitors.

Martin Braddock, Mark Furber, Keith Bowers, 2007, Journal of medicinal chemistry.