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The Journal of Organic Chemistry|May 11, 2013
Scaffold-divergent synthesis of ring-fused indoles, quinolines, and quinolones via iodonium-induced reaction cascadesRosliana Halim, Luigi Aurelio, Peter J Scammells, et al.Molecules (Basel, Switzerland)|July 2, 2021
Enantioenriched Positive Allosteric Modulators Display Distinct Pharmacology at the Dopamine D<sub>1</sub> ReceptorTim J Fyfe, Peter J Scammells, J Robert Lane, et al.The Journal of Organic Chemistry|December 6, 2003
Efficient N-demethylation of opiate alkaloids using a modified nonclassical Polonovski reactionKristy McCamley, Justin A Ripper, Robert D Singer, et al.Bioorganic & Medicinal Chemistry|September 1, 2004
New potent and selective A1 adenosine receptor agonistsSally A Hutchinson, Stephen P Baker, Joel Linden, et al.Biochemical Society Transactions|September 2, 2020
Driving antimalarial design through understanding of target mechanismPetar P S Calic, Mahta Mansouri, Peter J Scammells, et al.The Journal of Organic Chemistry|June 23, 2010
Two-step iron(0)-mediated N-demethylation of N-methyl alkaloidsGaik B Kok, Cory C Pye, Robert D Singer, et al.Organic & Biomolecular Chemistry|April 5, 2007
On the stability of 2-aminoselenophene-3-carboxylates: potential dual-acting selenium-containing allosteric enhancers of A1 adenosine receptor bindingKylee M Aumann, Peter J Scammells, Jonathan M White, et al.Bioorganic & Medicinal Chemistry|November 29, 2007
N6-substituted C5'-modified adenosines as A1 adenosine receptor agonistsT D Ashton, Stephen P Baker, Sally A Hutchinson, et al.Journal of Computer-Aided Molecular Design|April 25, 2012
Virtual screening using a conformationally flexible target protein: models for ligand binding to p38α MAPKNatalie B Vinh, Jamie S Simpson, Peter J Scammells, et al.Medchemcomm|August 16, 2018
Antimalarial drug discovery targeting apical membrane antigen 1Shane M Devine, Christopher A MacRaild, Raymond S Norton, et al.Pageof 15