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Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein-Protein Interaction.
J Med Chem. 2021 Apr 8;64(7):4071-4088. doi: 10.1021/acs.jmedchem.0c02188. Epub 2021 Mar 24.
J Med Chem. 2021.
PMID: 33761253
Expedient synthesis of an atypical oxazolidinone compound library.
Cully SJ, Storr TE, Rawling MJ, Abeysena IR, Hamza D, Jones G, Pearce CA, Quddus A, Lewis W, Stockman RA.
Cully SJ, et al.
Bioorg Med Chem. 2016 Nov 1;24(21):5249-5257. doi: 10.1016/j.bmc.2016.08.046. Epub 2016 Aug 27.
Bioorg Med Chem. 2016.
PMID: 27622748
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Combining two-directional synthesis and tandem reactions. Part 21: Exploitation of a dimeric macrocycle for chain terminus differentiation and synthesis of an sp(3)-rich library.
Storr TE, Cully SJ, Rawling MJ, Lewis W, Hamza D, Jones G, Stockman RA.
Storr TE, et al. Among authors: cully sj.
Bioorg Med Chem. 2015 Jun 1;23(11):2621-8. doi: 10.1016/j.bmc.2014.12.050. Epub 2014 Dec 29.
Bioorg Med Chem. 2015.
PMID: 25638497
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Facile access to a heterocyclic, sp(3)-rich chemical scaffold via a tandem condensation/intramolecular nitrone-alkene [3+2] cycloaddition strategy.
Rawling MJ, Storr TE, Bawazir WA, Cully SJ, Lewis W, Makki MS, Strutt IR, Jones G, Hamza D, Stockman RA.
Rawling MJ, et al. Among authors: cully sj.
Chem Commun (Camb). 2015 Aug 18;51(64):12867-70. doi: 10.1039/c5cc05070g.
Chem Commun (Camb). 2015.
PMID: 26169627
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