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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Jollymore-Hughes CT, Pottie IR, Martin E, Rosenberry TL, Darvesh S. Development of acetophenone ligands as potential neuroimaging agents for cholinesterases. Bioorganic & Medicinal Chemistry. PMID 27637382 DOI: 10.1016/J.Bmc.2016.08.048  0.314
2013 Macdonald IR, Jollymore CT, Reid GA, Pottie IR, Martin E, Darvesh S. Thioesters for the in vitro evaluation of agents to image brain cholinesterases. Journal of Enzyme Inhibition and Medicinal Chemistry. 28: 447-55. PMID 22233541 DOI: 10.3109/14756366.2011.647008  0.335
2011 Pottie IR, Nandaluru PR, Benoit WL, Miller DO, Dawe LN, Bodwell GJ. Synthesis of 6H-dibenzo[b,d]pyran-6-ones using the inverse electron demand Diels-Alder reaction. The Journal of Organic Chemistry. 76: 9015-30. PMID 21955052 DOI: 10.1021/jo201775e  0.527
2011 Pottie IR, Nandaluru PR, Bodwell GJ. An inverse electron-demand diels-alder-based total synthesis of urolithin M7 Synlett. 2245-2247. DOI: 10.1055/S-0030-1261203  0.524
2011 Macdonald I, Jollymore C, Pottie I, Martin E, Darvesh S. Synthesis and in vitro evaluation of N-Methylpiperidinyl thioesters as a model approach to the development of cholinesterase imaging agents Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.2085  0.314
2003 Abourahma H, Bodwell GJ, Lu J, Moulton B, Pottie IR, Walsh RB, Zaworotko MJ. Coordination polymers from calixarene-like [Cu 2(dicarboxylate)2]4 building blocks: Structural diversity via atropisomerism Crystal Growth and Design. 3: 513-519. DOI: 10.1021/Cg0340345  0.474
1999 Bodwell GJ, Pi Z, Pottie IR. Electron deficient dienes. 2. One step synthesis of a coumarin-fused electron deficient diene and its inverse electron demand Diels-Alder reactions with enamines Synlett. 477-479. DOI: 10.1055/S-1999-2645  0.54
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