Ricardo Resende

Modulation of drug‐linker design to enhance in vivo potency of homogeneous antibody‐drug conjugates

P. Williams, M. Bird, A. Jenkins, 2017, Journal of controlled release : official journal of the Controlled Release Society.

Incorporation of Hydrophilic Macrocycles Into Drug-Linker Reagents Produces Antibody-Drug Conjugates With Enhanced in vivo Performance

F.E.R. Jewitt, A. Jenkins, Ravindra Kumar Pathak, 2022, Frontiers in Pharmacology.

The synthesis and kinetic evaluation of aryl α-aminophosphonates as novel inhibitors of T. cruzi trans-sialidase.

Andrew G. Watts, A. Frasch, S. Crennell, 2018, European journal of medicinal chemistry.

Mechanism-Based Covalent Neuraminidase Inhibitors with Broad-Spectrum Influenza Antiviral Activity

Andrew G. Watts, S. Withers, P. Pilling, 2013, Science.

Sugar bislactones by one-step oxidative dimerisation with pyridinium chlorochromate versus regioselective oxidation of vicinal diols.

A. Rauter, J. Justino, F. V. Silva, 2004, Carbohydrate Research.

Palladium-catalysed allylic amination for the direct synthesis of epi-4-alkylamino-N-acetylneuraminic acid derivatives

Andrew G. Watts, Ricardo Resende, Christian Glover, 2009 .

Mechanism-Based Covalent Neuraminidase Inhibitors with Broad-Spectrum Influenza Antiviral Activity

Andrew G. Watts, S. Withers, P. Pilling, 2013, Science.