R. S. Holvey

Selective Targeting of the TPX2 Site of Importin-α Using Fragment-Based Ligand Design

Chris Abell, C. Abell, E. Valkov, 2015, ChemMedChem.

C–H functionalisation tolerant to polar groups could transform fragment-based drug discovery (FBDD)

Paul N. Mortenson, G. Chessari, R. S. Holvey, 2021, Chemical science.

Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein-Protein Interaction.

M. Noble, J. Endicott, G. Chessari, 2021, Journal of medicinal chemistry.

A safe and reliable procedure for the iododeamination of aromatic and heteroaromatic amines in a continuous flow reactor

R. S. Holvey, T. Underwood, Julia Madrzak, 2009 .