Publications

Key publications

1. Lucy, D., Purvis, G.S.D,. Zeboudj, L., Chatzopoulou, M., Recio, C., Bataille, C.J.R., Wynne, G.M., Greaves, D.R., and Russell, A.J. A Biased Agonist at Immunometabolic Receptor GPR84 Causes Distinct Functional Effects in Macrophages. ACS Chem. Biol. 2019, 14, 2055-2064. DOI: https://doi.org/10.1021/acschembio.9b00533

In collaboration with David Greaves' lab (Sir William Dunn School of Pathology) this study in ACS Chemical Biology reveals how biased signalling at the GPR84 receptor can result in differing regulation of immune cell chemotaxis.

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2. Quevedo, C.E., Cruz-Migoni, A., Bery, N., Miller, A.,Tanaka, T., Petch, D., Bataille, C.J.R., Lee, L.Y.W., Fallon, P.S., Tulmin, H., Ehebauer, M.T., Fernandez-Fuentes, N., Russell, A.J., Carr, S.B., Phillips, S.E.V., & Rabbitts, T.H. Small molecule inhibitors of RAS-effector protein interactions derived using an intracellular antibody fragment, Nature Communications, 2018, 9. DOI: 10.1038/s41467-018-05707-2

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This paper highlights a new strategy for targeting protein-protein interactions (PPIs) for the development of new small molecule therapeutics.
In collaboration with the Rabbitts Group (MRC Weatherall Institute of Molecular Medicine, WIMM) the paper describes a new approach using intracellular antibody fragments to block Protein-Protein Interactions (PPIs), using the fragments for target validation in disease models, and developing new small molecules against the PPI epitope. The approach was used to identify RAS-binding compounds with the aim of developing potential treatments for RAS-dependent cancers.

3. Kerr, A.G.; Tam, L.C.S.; Hale, A.B.; Cioroch, M.; Douglas, G.; Agkatsev, S.; Hibbitt, O.; Mason, J.; Holt-Martyn, J.; Bataille, C.J.R.; Wynne, G.M.; Channon, K.M.; Russell, A.J. and Wade-Martins, R. A genomic DNA reporter screen identifies squalene synthase inhibitors which act cooperatively with statins to upregulate the low-density lipoprotein receptor. Journal of Pharmacology and Experimental Therapeutics, 2017, 361 (3), 417-428. DOI: https://doi.org/10.1124/jpet.116.239574

Joint programme of research with the Wade-Martins group. The discovery of a novel series of small molecules as upregulators of the low-lipodensity receptor (LDLR) in vitro and in vivo, their molecular mechanism of action and their cooperative effects with statins elucidated in vitro. They thus may serve as a means to treat diseases such as familial hypercholesterolaemia which cannot always be adequately controlled with statins alone.

4. Partridge, FA.; Murphy, EA.; Willis, NJ.; Bataille, CJR.; Forman, R.; Heyer-Chauhan, N.; Marinič, B.; Sowood, DJC.; Wynne, GM.; Else, KJ.; Russell, AJ.; Sattelle, DB. Dihydrobenz[e][1,4]oxazepin-2(3H)-ones, a new anthelmintic chemotype immobilising whipworm and reducing infectivity in vivo. PLoS Negl Trop Dis, 2017, 11(2): e0005359. DOI:10.1371/ journal.pntd.0005359.

Joint programme of research with Else and Sattelle in a multiway collaborative open innovation drug discovery programme. The discovery of a novel series of small molecules as anthelmintics with activity both in vitro and in vivo against whipworm, an inadequately controlled disease prevalent in developing countries.

5. Gianella-Borradori, M.; Christou, I.; Bataille, C. J. R.; Cross, R. L.; Wynne, G. M.; Greaves, D. R.; Russell, A. J. Ligand-based virtual screening identifies a family of selective cannabinoid receptor 2 agonists. Bioorg. Med. Chem. 2015, 23, 241-263. DOI: https://doi.org/10.1016/j.bmc.2014.11.002

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Joint programme of research with Greaves. The discovery of a novel series of small molecules as highly selective cannabinoid receptor 2 (CB2R) agonists with downstream application as endocannabinoid modulating anti-inflammatory agents. The highly selective CB2R agonists have been subsequently used to demonstrate the polypharmacology of previously described CB2R agonists (see Taylor et al., Scientific Rep. 2015).

6. Davies, S. G.; Kennewell, P. D.; Russell, A. J.; Seden, P. T.; Westwood, R.; Wynne, G. M. Stemistry: The Control of Stem Cells in Situ Using Chemistry. J. Med. Chem. 2015, 58, 2863-2894. DOI: 10.1021/jm500838d

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A field-defining invited and peer-reviewed perspective article introducing the concept of “Stemistry”: in situ stem cell chemistry, a term now adopted by the field. Provides a critical overview of the work of our group and others developing drugs for regenerative medicine by targeting and augmenting endogenous repair pathways directly in vivo.

7. Laurieri, N.; Crawford, M. H. J.; Kawamura, A.; Westwood, I. M.; Robinson, J.; Fletcher, A. M.; Davies, S. G.; Sim, E. and Russell, A. J. Small Molecule Colorimetric Probes for Specific Detection of Human Arylamine N-Acetyltransferase 1, a Potential Breast Cancer Biomarker. J. Am. Chem. Soc. 2010, 132, 3238–3239. DOI: 10.1021/ja909165u

The paper describes a novel and simple mechanism through which a small molecule ligand’s optical absorption properties could be used to specifically detect binding to a native protein. The molecules were subsequently developed into tools to quantify this specific protein within tumour cells. Highlighted in Anslyn, E. Supramolecular and Chemical Cascade Approaches to Molecular Sensing, J. Am. Chem. Soc. 2010, 132, 15833–15835; JACS Select #10 “Supramolecular and Chemical Cascade Approaches to Molecular Sensing”.

8. Soncin, F.; Mohamet, L.; Eckardt, D.; Ritson, S.; Eastham, A. M.; Spencer, H.; Bobola, N.; Russell, A. J.; Davies, S. G.; Kemler, R.; Merry, C. L. R. and Ward, C. M. Abrogation of E-cadherin mediated cell-cell contact in mouse embryonic stem cells results in reversible LIF-independent self-renewal. Stem Cells, 2009, 27, 2069–2080. DOI: 10.1002/stem.134

Dogma-challenging paper that demonstrated by genetic and chemical means that embryonic stem cells (ESCs) could be cultured in a contact-independent manner while maintaining viability and pluripotency. Our research implemented the chemical-induced cell-cell segregation aspect – specifically targeting E-cadherin. This work has been instrumental in enabling scale-up culture of mouse ESCs and, importantly, subsequent translation to human cells.

Book chapters

Davies, S.G., Kennewell, P.D., Russell, A.J., Silpa, L., Westwood, R., and Wynne, G.M. Regenerative Medicine. Comprehensive Medicinal Chemistry III, Chackalamannil, S., Rotella, D., and Ward, S.E. (Ed.). Elsevier Ltd, 2017, ISBN: 978-0-12-803201-5.

Russell, A. J. and Wynne, G. M.
Drug Discovery Approaches for Rare Neuromuscular Diseases. Orphan Drugs and Rare Diseases, Palmer, M. and Pryde, D. (Ed.). Royal Society of Chemistry, 2014, ISBN: 978-1-84973-806-4.

Davies, S. G. and Russell, A. J.
Chemical Biology of Stem Cell Modulation
New Frontiers in Chemical Biology, Bunnage, M. E. (Ed.). Royal Society of Chemistry,
2011, ISBN: 184973125X.

All publications
2020

98 Wilkinson, I.V.L., Reynolds, J.K., Galana, S.R.G., Vuorinena, A., Sills, A.J., Piresa, E., Wynne, G.M., Wilson, F.X., Russell, A.J. Characterisation of utrophin modulator SMT C1100 as a non-competitive inhibitor of firefly luciferase. Bioorganic Chemistry, 94, 2020, 103395. DOI: https://doi.org/10.1016/j.bioorg.2019.103395

2019

97 Wilkinson. I.V.L., Perkins, K.J., Dugdale, H., Moir, L., Vuorinen, A., Chatzopoulou, M., Squire, S.E., Monecke, S., Lomow, A., Geese, M., Charles, P.D., Burch, P., Tinsley, J.M., Wynne, G.M., Davies, S.G., Wilson, F.X., Rastinejad, F., Mohammed, S., Davies, K.E., Russell, A.J. Chemical Proteomics and Phenotypic Profiling Identifies the Aryl Hydrocarbon Receptor as a Molecular Target of the Utrophin Modulator Ezutromid. Angewandte Chemie, 2019. DOI: https://doi.org/10.1002/anie.201912392

96 Chatzopoulou M., Claridge T.D.W., Davies K.E., Davies S.G., Elsey D., Emer E., Fletcher A.M., Harriman S., Robinson N., Rowley J., Russell A.J., Tinsley J., Weaver R., Wilkinson I., Willis N., Wilson F., Wynne G.M.Isolation, structural identification, synthesis, and pharmacological profiling of 1,2-trans-dihydro-1,2-diol metabolites of the utrophin modulator ezutromid. Journal of Medicinal Chemistry. 2019. DOI: https://doi.org/10.1021/acs.jmedchem.9b01547

95 Lucy, D., Purvis, G.S.D,. Zeboudj, L., Chatzopoulou, M., Recio, C., Bataille, C.J.R., Wynne, G.M., Greaves, D.R., and Russell, A.J. A Biased Agonist at Immunometabolic Receptor GPR84 Causes Distinct Functional Effects in Macrophages. ACS Chem. Biol. 2019, 14, 2055-2064. DOI: https://doi.org/10.1021/acschembio.9b00533

94 Cruz-Migoni A; Canning P; Quevedo CE; Bataille CJR; Bery N; Miller A; Russell AJ; Phillips SEV; Carr SB; Rabbitts TH. Structure-based development of new RAS-effector inhibitors from a combination of active and inactive RAS-binding compounds. Proceedings of the National Academy of Sciences of the United States of America, 2019, 116, 2545-2550. DOI: https://doi.org/10.1073/pnas.1811360116


2018

93 Partridge, F.A., Forman, R. Willis, N.J., Bataille, C.J.R., Murphy, E.A., Brown, A.E., Heyer-Chauhan, N., Marinič, B., Sowood, D.J.C., Wynne, G.M., Else, K.J., Russell, A.J., and Sattelle, D.B. 2,4-Diaminothieno[3,2-d]pyrimidines, a new class of anthelmintic with activity against adult and egg stages of whipworm. PLoS Neglected Tropical Diseases, 2018, DOI: https://doi.org/10.1371/journal.pntd.0006487

92 Recio, C., Lucy, D., Purvis, G.S.D., Iveson, P., Zeboudj, L., Iqbal, A.J., Lin, D., O'Callaghan, C., Davison, L., Griesbach, E., Russell, A.J., Wynne, G.M., Dib, L., Monaco, C., and Greaves, D.R. Activation of the Immune-Metabolic Receptor GPR84 Enhances Inflammation and Phagocytosis in Macrophages. Front. Immunol. 2018, 9:1419. DOI: 10.3389/fimmu.2018.01419

91 Partridge⁠⁠, ⁠F. A.; Brown⁠⁠, ⁠A. E.; Buckingham⁠⁠, S. D.⁠; Willis⁠⁠, ⁠N. J.; Wynne⁠, G. W.; Forman⁠, R.; Else⁠, K. J.; Morrison⁠, A.; Matthews⁠, J. B.; Russell, A. J.; Lomas⁠⁠, D. J.; Sattelle, D. B. An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes. Int. J. Parasitol.: Drugs and Drug Resistance, 2018, 8, 8-21. DOI: 10.1016/j.ijpddr.2017.11.004

90 Bery, N., Cruz-Migoni, A., Bataille, C.J.R., Quevedo, C.E., Tulmin, H., Miller, A., Russell, A.J., Phillips, S.E.V., Carr, S.B., and Rabbitts, T.H. BRET-based RAS biosensors that show a novel small molecule is an inhibitor of RAS-effector protein-protein interactions. eLife, 2018;7:e37122 DOI: 10.7554/eLife.37122

89 Stefaniak, J., Lewis, A.M., Conole, D., Galan, S.R.G., Bataille, C.J.R., Wynne, G.M., Castaldi, M.P., Lundbäck, T., Russell, A.J., and Huber, K.V.M. Chemical Instability and Promiscuity of Arylmethylidenepyrazolinone-Based MDMX Inhibitors. ACS Chem. Biol. 2018, DOI: 10.1021/acschembio.8b00665

88 Venturi, E., Lindsay, C., Lotteau, S., Yang, Z., Steer, E., Witschas, K., Wilson, A. D., Wickens, J. R., Russell, A. J., Steele, D., Calaghan, S., and Sitsapesan, R. Simvastatin activates single skeletal RyR1 channels but exerts more complex regulation of the cardiac RyR2 isoform. British Journal of Pharmacology, 2018. DOI: 10.1111/bph.14136.

87 Quevedo, C.E., Cruz-Migoni, A., Bery, N., Miller, A.,Tanaka, T., Petch, D., Bataille, C.J.R., Lee, L.Y.W., Fallon, P.S., Tulmin, H., Ehebauer, M.T., Fernandez-Fuentes, N., Russell, A.J., Carr, S.B., Phillips, S.E.V., & Rabbitts, T.H. Small molecule inhibitors of RAS-effector protein interactions derived using an intracellular antibody fragment, Nature Communications, 2018, 9. DOI: 10.1038/s41467-018-05707-2

86 Chatzopoulou, M., Martínez, R.F., Willis, N.J., Claridge, T.D.W., Wilson, F.X., Wynne, G.W., Davies, S.G. and Russell, A.J. The Dimroth rearrangement as a probable cause for structural misassignments in imidazo[1,2-a]pyrimidines: A 15N-labelling study and an easy method for the determination of regiochemistry. Tetrahedron, 2018, 74(38), 5280-5288. DOI: https://doi.org/10.1016/j.tet.2018.06.033

85 Recio, C., Lucy, D., Iveson, P., Iqbal, A.J., Valaris, S., Wynne, G.M., Russell, A.J., Choudhury, R., O'Callaghan, C., Monaco, C., and Greaves, D.R. The Role of Metabolite-sensing G Protein-Coupled Receptors in inflammation and metabolic disease. Antioxidants & Redox Signaling 2018, DOI: 10.1089/ars.2017.7168.


2017

84 Kerr, A.G.; Tam, L.C.S.; Hale, A.B.; Cioroch, M.; Douglas, G.; Agkatsev, S.; Hibbitt, O.; Mason, J.; Holt-Martyn, J.; Bataille, C.J.R.; Wynne, G.M.; Channon, K.M.; Russell, A.J. and Wade-Martins, R. A genomic DNA reporter screen identifies squalene synthase inhibitors which act cooperatively with statins to upregulate the low-density lipoprotein receptor. Journal of Pharmacology and Experimental Therapeutics, 2017, 361 (3), 417-428. DOI: https://doi.org/10.1124/jpet.116.239574

83 Partridge, FA.; Murphy, EA.; Willis, NJ.; Bataille, CJR.; Forman, R.; Heyer-Chauhan, N.; Marinič, B.; Sowood, DJC.; Wynne, GM.; Else, KJ.; Russell, AJ.; Sattelle, DB. Dihydrobenz[e][1,4]oxazepin-2(3H)-ones, a new anthelmintic chemotype immobilising whipworm and reducing infectivity in vivo. PLoS Negl Trop Dis, 2017, 11(2): e0005359. DOI:10.1371/ journal.pntd.0005359.

82 Brambilla, M, Brennan, M.B., Csatayová, K., Davies, S.G., Fletcher, A.M., Kennett, A.M.R., Lee, J.A., Roberts, P.M., Russell, A.J., Thomson, J.E. Probing Competitive and Co-operative Hydroxyl and Ammonium Hydrogen-Bonding Directed Epoxidations. J Org Chem, 2017, 82, 10297-10309. DOI: 10.1021/acs.joc.7b01774.

81 Tempone, A.G.; Ferreira, D.D.; Lima L.M.; Silva, T.A.C.; Borborema, S.E.T.; Reima, J.Q.; Galuppo, M.K.; Guerra, J.M.; Russell, A.J.; Wynne, G.M.; Lai, R.Y.L.; Cadelis, M.M.; Copp, B.R. Efficacy of a series of alpha-pyronederivatives against Leishmania (L.) infantum and Trypanosoma cruzi. European Journal of Medicinal Chemistry, 2017, 139, 947-960. DOI: https://doi.org/10.1016/j.ejmech.2017.08.055

80 Muntoni, F.; Maresh, K.; Davies, K.; Harriman, S.; Layton, G.; Rosskamp, R.; Russell, A.; Tejura, B.; Tinsley, J. PhaseOut DMD: a Phase 2, proof of concept, clinical study of utrophin modulation with ezutromid. Neuromuscular Dis. 2017, 27, S217. DOI: https://doi.org/10.1016/j.nmd.2017.06.443.

79 Davies, S.G., Kennewell, P.D., Russell, A.J., Silpa, L., Westwood, R., and Wynne, G.M. Regenerative Medicine. Comprehensive Medicinal Chemistry III, Chackalamannil, S., Rotella, D., and Ward, S.E. (Ed.). Elsevier Ltd, 2017, ISBN: 978-0-12-803201-5.

78 Bataille, CJR.; Brennan, MB.; Byrne, S.; Davies, SG.; Durbin, M.; Fedorov, O.; Huber, KVM,; Jones, AM.; Knapp, S.; Liu, G.; Nadali, A.; Quevedoa, CE.; Russell, AJ.; Walker, RG.; Westwood, R.; Wynne, GW. Thiazolidine derivatives as potent and selective inhibitors of the PIM kinase family. Bioorganic and Medicinal Chemistry, 2017. DOI: http://dx.doi.org/10.1016/j.bmc.2017.02.056


2016

77 Zervou, S.; Whittington, H.J.; Russell, A.J. and Lygate, C.A. Augmentation of creatine in the heart. Mini-reviews in Medicinal Chemistry. 2016, 16, 19-28. DOI: 10.2174/1389557515666150722102151

76 Russell, A.J. and Silpa, L. Chemical-Induced Naive Pluripotency. Cell Chemical Biology, 2016, 23, 532-534. DOI: 10.1016/j.chembiol.2016.05.002.

75 McIntyre, A.; Hulikova, A.; Ledaki, I.; Snell, C.; Singleton, D.; Steers, G.; Seden, P.; Jones, D.; Bridges, E.; Winfield, S.; Li, J.L.; Russell, A.; Switch, P.; Harris, A.L. Disrupting Hypoxia-Induced Bicarbonate Transport Acidifies Tumor Cells and Suppresses Tumor Growth. Cancer Res, 2016, 76, 3744–55. DOI: 10.1158/0008-5472.CAN-15-1862

74 Davies, S. G.; Goddard, E, C.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Thomson, J. E.; Withey, J. M. Strategies for the construction of morphinan alkaloid AB-rings: regioselective Friedel-Crafts-type cyclisations of γ-aryl-β-benzoylamido acids with asymmetrically substituted γ-aryl rings. Tetrahedron: Asymmetry, 2016, 27, 274. DOI: https://doi.org/10.1016/j.tetasy.2016.02.010


2015

73 Davies, S. G.; Goddard, E. C.; Roberts, P. M.; Russell, A. J.; Thomson, J. E. Enantiopure 3-amino substituted 1-indanones, 1-tetralones and 1-benzosuberones via Friedel-Crafts cyclisation of ω-aryl-β-benzamido acids. Synlett, 2015. DOI: 10.1055/s-0034-1380675.

72 Brennan, M. B.; Davies, S. G.; Fletcher, A. M.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Thomson, J. E. Epoxidation of trans-4-aminocyclohex-2-en-1-ol derivatives: competition of hydroxyl-directed and ammonium-directed pathways. Aust. J. Chem. 2015, 68, 610-621. DOI: https://doi.org/10.1071/CH14531

71 Gianella-Borradori, M.; Christou, I.; Bataille, C. J. R.; Cross, R. L.; Wynne, G. M.; Greaves, D. R.; Russell, A. J. Ligand-based virtual screening identifies a family of selective cannabinoid receptor 2 agonists. Bioorg. Med. Chem. 2015, 23, 241-263. DOI: https://doi.org/10.1016/j.bmc.2014.11.002

70 Taylor, L.; Christou, I.; Kapellos, T. S.; Buchan, A.; Brodermann, M. H.; Gianella-Borradori, M.; Russell, A.; Iqbal, A. J.; Greaves, D. R. Primary macrophage chemotaxis induced by cannabinoid receptor 2 agonists occurs independently of the CB2 receptor. Scientific Rep. 2015, 5, 10682. DOI: 10.1038/srep10682

69 Guiraud, S.; Squire, S. E.; Edwards, B.; Chen, H.; Burns, D. T.; Shah, N.; Babbs, A.; Davies, S. G.; Wynne, G. M.; Russell, A. J.; Elsey, D.; Wilson, F. X.; Tinsley, J. M.; Davies, K. E. Second-generation compound for the modulation of utrophin in the therapy of DMD. Hum. Mol. Genet. 2015, DOI: 10.1093/hmg/ddv154.

68 Davies, S. G.; Kennewell, P. D.; Russell, A. J.; Seden, P. T.; Westwood, R.; Wynne, G. M. Stemistry: The Control of Stem Cells in Situ Using Chemistry. J. Med. Chem. 2015, 58, 2863-2894. DOI: 10.1021/jm500838d

67 Brennan, M.; Csatayová, K.; Davies, S. G.; Fletcher, A. M.; Green, W. D.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Thomson, J. E. Syntheses of dihydroconduramines (±)-B-1, (±)-E-1 and (±)-F-1 via diastereoselective epoxidation of N-protected 4-aminocyclohex-2-en-1-ols. J. Org. Chem. 2015, DOI: 10.1021/acs.joc.5b00716.

66 Clunie-O’Connor, C.; Smits, A.M.; Antoniades, C.; Russell, A.J.; Yellon, D.M.; Goumans, M-J.; Riley, P.R. The Derivation of Primary Human Epicardium-Derived Cells. Curren. Protoc. Stem Cell Biol. 2015, 35: 2C.5.1 - 2C.5.x. DOI: 10.1002/9780470151808.sc02c05s35


2014

65 Laurieri, N.; Kawamura, A.; Westwood, I. M.; Varney, A.; Morris, E.; Russell, A. J.; Stanley, L. A.; Sim, E. Differences between murine arylamine N-acetyltransferase type 1 and human arylamine N-acetyltransferase type 2 defined by substrate specificity and inhibitor binding. BMC Pharmacol. Toxicol. 2014, 15, 68. DOI: 10.1186/2050-6511-15-68

64 Russell, A. J. and Wynne, G. M.
Drug Discovery Approaches for Rare Neuromuscular Diseases. Orphan Drugs and Rare Diseases, Palmer, M. and Pryde, D. (Ed.). Royal Society of Chemistry, 2014, ISBN: 978-1-84973-806-4.

63 Abuhammad, A.; Fullam, E.; Bhakta, S.; Russell, A. J.; Morris, G. M.; Finn, P. W.; Sim, E. Exploration of Piperidinols as Potential Antitubercular Agents. Molecules, 2014, 19, 16274–16290. DOI: 10.3390/molecules191016274

62 Laurieri, N.; Dairou, J.; Egleton, J. E.; Stanley, L. A.; Russell, A. J.; Dupret, J. M.; Sim, E.; Rodrigues-Lima, F. From Arylamine N-Acetyltransferase to Folate-Dependent Acetyl CoA Hydrolase: Impact of Folic Acid on the Activity of (HUMAN)NAT1 and Its Homologue (MOUSE)NAT2. PLoS One, 2014, 9, e96370. DOI: 10.1371/journal.pone.0096370

61 Egleton, J. E.; Thinnes, C. C.; Seden, P. T.; Laurieri, N.; Lee, S. P.; Hadavizadeh, K. S.; Measures, A. R.; Jones, A. M.; Thompson, S.; Varney, A.; Wynne, G. M.; Ryan, A.; Sim, E.; Russell, A. J. Structure-activity relationships and colorimetric properties of specific probes for the putative cancer biomarker human arylamine N-acetyltransferase 1. Bioorg. Med. Chem. 2014, 22, 3030–3054. DOI: 10.1016/j.bmc.2014.03.015

60 Davies, S. G. and Russell, A. J.
Chemical Biology of Stem Cell Modulation
New Frontiers in Chemical Biology, Bunnage, M. E. (Ed.). Royal Society of Chemistry,
2011, ISBN: 184973125X.


2013

59 Lufino, M. M. P.; Silva, A. M.; Németh, A. H.; Alegre-Abarrategui J.; Russell A. J.; Wade-Martins, R. A. A GAA repeat expansion reporter model of Friedreich's ataxia recapitulates the genomic context and allows rapid screening of therapeutic compounds. Human Mol. Genet. 2013, 22, 5173–5187. DOI: 10.1093/hmg/ddt370

58 Laurieri, N.; Egleton, J.E.; Varney, A.; Thinnes, C. C.; Quevedo, C. E.; Seden, P.T.; Thompson, S.; Rodrigues-Lima, F.; Dairou, J.; Dupret, J.-M.; Russell, A. J.; Sim, E. A Novel Color Change Mechanism for Breast Cancer Biomarker Detection: Naphthoquinones as Specific Ligands of Human Arylamine N-Acetyltransferase 1. PLoS One, 2013, 8, e70600. DOI: 10.1371/journal.pone.0070600

57 Fullam, E.; Talbot, J.; Abuhammed, A.; Westwood, I.; Davies, S. G.; Russell, A. J.; Sim, E. Design, synthesis and structure-activity relationships of 3,5-diaryl-1H-pyrazoles as inhibitors of arylamine N-acetyltransferase. Bioorg. Med. Chem. Lett. 2013, 23, 2759–2764. DOI: 10.1016/j.bmcl.2013.02.052

56 Hewings, D. S.; Fedorov, O.; Filippakopoulos, P.; Martin, S.; Picaud, S.; Tumber, A.; Wells, C.; Olcina, M. M.); Freeman, K.; Gill, A.; Ritchie, A. J.; Sheppard, D. W.; Russell, A. J.; Hammond, E. M.; Knapp, S.; Brennan, P. E.; Conway, S. J. Optimization of 3,5-Dimethylisoxazole Derivatives as Potent Bromodomain Ligands. J. Med. Chem. 2013, 56, 3217–3227. DOI: 10.1021/jm301588r

55 Russell, A. J. Regenerative Medicinal Chemistry: The in Situ Control of Stem Cells. ACS Med. Chem. Lett. 2013, 4, 365–368. DOI: 10.1021/ml400110b

54 Claridge, T. D. W.; Davies, S. G.; Kruchinin, D.; Odell, B.; Roberts, P. M.; Russell, A. J.; Thomson, J. E.; Toms, S. M. Solution phase structures of enantiopure and racemic lithium N-benzyl-N-(α-methylbenzyl)amide in THF: Low temperature Li and N NMR spectroscopic studies. Tetrahedron Asymmetry, 2013, 24, 947–952. DOI: https://doi.org/10.1016/j.tetasy.2013.07.001


2012

53 Abuhammad, A.; Fullam, E.; Lowe, E. D.; Staunton, D.; Kawamura, A.; Westwood, I. M.; Bhakta, S.; Garner, A. C.; Wilson, D. L.; Seden, P. T.; Davies, S. G.; Russell, A. J.; Garman, E. F.; Sim, E. Piperidinols That Show Anti-Tubercular Activity as Inhibitors of Arylamine N-Acetyltransferase: An Essential Enzyme for Mycobacterial Survival Inside Macrophages. PLoS One, 2012, 7, e52790. DOI: 10.1371/journal.pone.0052790

52 Davies, S. G.; Fletcher, A. M.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Taylor, R. J.; Thomson, A. D.; Thomson, J. E. Polysubstituted Piperidines via Iodolactonization: Application to the Asymmetric Synthesis of (+)-Pseudodistomin D. Org. Lett. 2012, 14, 1672–1675. DOI: 0.1021/ol300209s


2011

51 Abraham, E.; Claridge, T. D. W.; Davies, S. G.; Odell, B.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Smith, L. J.; Storr, H. R.; Sweet, M. J.; Thompson, A. L.; Thomson, J. E.; Tranter, G. E.; Watkin, D. J. A systematic study of the solid state and solution phase conformational preferences of beta-peptides derived from C(3)-alkyl substituted transpentacin derivatives. Tetrahedron: Asymmetry, 2011, 22, 69–100. DOI: https://doi.org/10.1016/j.tetasy.2010.12.007

50 Fullam, E.; Abuhammad, A.; Wilson, D. L.; Davies, S. G.; Russell, A. J. and Sim, E. Analysis of beta-amino alcohols as inhibitors of the potential anti-tubercular target N-acetyltransferase. Bioorg. Med. Chem. Lett. 2011, 21, 1185–1190. DOI: 10.1016/j.bmcl.2010.12.099

49 Davies, S. G.; Fletcher, A. M.; Hughes, D. G.; Lee, J. A.; Price, P. D.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Thomson, J. E.; Williams, O. M. H. Asymmetric synthesis of piperidines and octahydroindolizines using a one-pot ring-closure/N-debenzylation procedure. Tetrahedron 2011, 67, 9975–9992. DOI: https://doi.org/10.1016/j.tet.2011.09.038

48 Li, J. L.; Sainson, R. C. A.; Oon, C. E.; Turley, H.; Leek, R.; Sheldon, H.; Bridges, E.; Shi, W.; Snell, C.; Bowden, E. T.; Wu, H. R.; Chowdhury, P. S.; Russell, A. J.; Montgomery, C. P.; Poulsom, R. and Harris, A. L. DLL4-Notch Signaling Mediates Tumor Resistance to Anti-VEGF Therapy In Vivo. Cancer Res. 2011, 71, 6073–6083. DOI: 10.1158/0008-5472.CAN-11-1704

47 Csatayova, K.; Davies, S. G.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Thomson, J. E.; Wilson, D. L. Highly Diastereoselective and Stereodivergent Dihydroxylations of Acyclic Allylic Amines: Application to the Asymmetric Synthesis of 3,6-Dideoxy-3-amino-L-talose. Org. Lett. 2011, 13, 2606–2609. DOI: 10.1021/ol200717n

46 Westwood, I. M.; Kawamura, A.; Russell, A. J.; Sandy, J.; Davies S. G. and Sim, E. Novel Small-Molecule Inhibitors of Arylamine N-Acetyltransferases: Drug Discovery by High Throughput Screening. Combi. Chem. High Throughput Screening 2011, 14, 117–124. DOI: 10.2174/138620711794474051

45 Davies, S. G. and Russell, A. J.
Chemical Biology of Stem Cell Modulation
New Frontiers in Chemical Biology, Bunnage, M. E. (Ed.). Royal Society of Chemistry,
2011, ISBN: 184973125X.


2010

44 Abraham, E.; Bailey, C. W.; Claridge, T. D. W.; Davies, S. G.; Ling, K. B.; Odell, B.; Rees, T. L.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Smith, L. J.; Storr, H. R.; Sweet, M. J.; Thompson, A. L.; Thomson, J. E.; Tranter, G. E.; Watkin, D. J. A systematic study of the solid state and solution phase conformational preferences of beta-peptides derived from transpentacin. Tetrahedron: Asymmetry 2010, 21, 1797–1815. DOI: https://doi.org/10.1016/j.tetasy.2010.12.007

43 Bagal, S. K.; Davies, S. G.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Scott, P. M. and Thomson, J. E. An Oxidation and Ring Contraction Approach to the Synthesis of (+/-)-1-Deoxynojirimycin and (+/-)-1-Deoxyaltronojirimycin. Org. Lett. 2010, 12, 136–139. DOI: 10.1021/ol902533b

42 Davies, S. G.; Hughes, D. G.; Price, P. D.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Thomson, J. E. And Williams, O. M. H. Asymmetric Synthesis of Piperidines and Octahydroindolizines. Synlett 2010, 567–570. DOI: https://doi.org/10.1016/j.tet.2011.09.038

41 Csatayova, K.; Davies, S. G.; Lee, J. A.; Ling, K. B.; Roberts, P. M.; Russell, A. J.; Thomson, J. E. Chemo- and diastereoselective cyclopropanation of allylic amines and carbamates. Tetrahedron 2010, 66, 8420–8440. DOI: https://doi.org/10.1016/j.tet.2010.08.055

40 Bentley, S. A.; Davies, S. G.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Thomson, J. E.; Toms, S. M. Conjugate addition of lithium N-tert-butyldimethylsilyloxy-N-(alpha-methylbenzyl)amide: asymmetric synthesis of beta(2,2,3)-trisubstituted amino acids. Tetrahedron, 2010, 66, 4604–4620. DOI: https://doi.org/10.1016/j.tet.2010.04.027

39 Westwood, I. M.; Bhakta, S.; Russell, A. J.; Fullam, E.; Anderton, M. C.; Kawamura, A.; Mulvaney, A. W.; Vickers, R. J.; Bhowruth, V.; Besra, G. S.; Lalvani, A.; Davies, S. G. and Sim, E. Identification of arylamine N-acetyltransferase inhibitors as an approach towards novel anti-tuberculars. Protein & Cell, 2010, 1, 82-95. DOI: 10.1007/s13238-010-0006-1

38 Laurieri, N.; Crawford, M. H. J.; Kawamura, A.; Westwood, I. M.; Robinson, J.; Fletcher, A. M.; Davies, S. G.; Sim, E. and Russell, A. J. Small Molecule Colorimetric Probes for Specific Detection of Human Arylamine N-Acetyltransferase 1, a Potential Breast Cancer Biomarker. J. Am. Chem. Soc. 2010, 132, 3238–3239. DOI: 10.1021/ja909165u

37 Csatayova, K.; Davies, S. G.; Lee, J. A.; Ling, K. B.; Roberts, P. M.; Russell, A. J.; Thomson, J. E. Syntheses of trans-SCH-A and cis-SCH-A via a Stereodivergent Cyclopropanation Protocol. Org. Lett. 2010, 12, 3152–3155. DOI: 10.1021/ol101295t

36 Davies, S. G.; Ling, K. B.; Roberts, P. M.; Russell, A. J.; Thomson, J. E.; Woods, P. A. The stereodivergent aziridination of allylic carbamates, amides and sulphonamides. Tetrahedron 2010, 66, 6806–6813. DOI: https://doi.org/10.1016/j.tet.2010.06.059

35 Cresswell, A. J.; Davies, S. G.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Thomson, J. E.; Tyte, M. J. beta-Fluoroamphetamines via the Stereoselective Synthesis of Benzylic Fluorides. Org. Lett. 2010, 12, 2936–2939. DOI: 10.1021/ol100862s


2009

34 Pettigrew, D. M.; Roversi, P.; Davies, S. G; Russell, A. J. and Lea, S. M. A structural study of the interaction between the Dr haemagglutinin DraE and derivatives of chloramphenicol. Acta Cryst. D 2009, 65, 513–522. DOI: 10.1107/S0907444909005113

33 Soncin, F.; Mohamet, L.; Eckardt, D.; Ritson, S.; Eastham, A. M.; Spencer, H.; Bobola, N.; Russell, A. J.; Davies, S. G.; Kemler, R.; Merry, C. L. R. and Ward, C. M. Abrogation of E-cadherin mediated cell-cell contact in mouse embryonic stem cells results in reversible LIF-independent self-renewal. Stem Cells, 2009, 27, 2069–2080. DOI: 10.1002/stem.134

32 Bond, C. W.; Cresswell, A. J.; Davies, S. G.; Fletcher, A. M.; Kurosawa, W.; Lee, J. A.; Roberts, P. M.; Russell, A. J.; Smith, A. D. and Thomson, J. E. Ammonium-Directed Oxidation of Cyclic Allylic and Homoallylic Amines. J. Org. Chem. 2009, 74, 6735–6748. DOI: 10.1021/jo9012783

31 Torabi Kachoosangi, R.; Musameh, M. M.; Abu-Yousef, I.; Yousef, J. M.; Kanan, S. M.; Xiao, L.; Davies, S. G.; Russell, A. and Compton, R. G. Carbon Nanotube - Ionic Liquid Composite Sensors and Biosensors. Anal. Chem. 2009, 81, 435–442. DOI: 10.1021/ac801853r

30 Davies, S. G.; Durbin, M. J; Goddard, E. C.; Kelly, P. M.; Kurosawa, W.; Lee, J. A.; Nicholson, R. L.; Price, P. D.; Roberts, P. M.; Russell, A. J.; Scott, P. M. and Smith, A. D. Double diastereoselective conjugate addition of homochiral lithium amides to homochiral α,β-unsaturated esters containing cis- and trans-dioxolane units. Org. Biomol. Chem. 2009, 7, 761–776. DOI: 10.1039/B818298A

29 Wilkinson, R. N.; Gering, M.; Russell, A. J.; Davies, S. G.; Kimelman, D. and Patient, R. Hedgehog and Bmp Polarize Hematopoietic Stem Cell Emergence in the Zebrafish Dorsal Aorta. Dev. Cell. 2009, 16, 909–916. DOI: 10.1016/j.devcel.2009.04.014

28 Aciro, C.; Davies, S. G.; Kurosawa, W.; Roberts, P. M.; Russell, A. J. and Thomson, J. E. Highly diastereoselective anti-dihydroxylation of 3-N,N-dibenzylaminocyclohex-1-ene N-oxide. Org. Lett. 2009, 11, 1333–1336. DOI: 10.1021/ol900114b

27 Davies, S. G.; Nicholson, R. L.; Price, P. D.; Roberts, P. M.; Russell, A. J.; Savory, E. D.; Smith, A. D. and Thomson, J. E. Iodine-mediated ring-closing iodoamination with concomitant N-debenzylation for the asymmetric synthesis of polyhydroxylated pyrrolidines. Tetrahedron: Asymmetry, 2009, 20, 758–772. DOI: https://doi.org/10.1016/j.tetasy.2009.02.014

26 Russell, A. J.; Westwood, I. M.; Crawford, M. C.; Robinson, J.; Kawamura, A.; Redfield, C.; Lowe, E. D.; Laurieri, N.; Davies, S. G. and Sim, E. Selective small molecule inhibitors of the potential breast cancer marker, human arylamine N-acetyltransferase 1, and its murine homologue, mouse arylamine N-acetyltransferase 2. Bioorg. Med. Chem. 2009, 17, 905–918. DOI: 10.1016/j.bmc.2008.11.032

25 Lack, N. A.; Kawamura, A.; Fullam, E.; Laurieri, N.; Beard, S.; Russell, A. J.; Evangelopoulos, D.; Westwood I. and Sim, E. Temperature stability of proteins essential for the intracellular survival of Mycobacterium tuberculosis. Biochem. J. 2009, 418, 369–378. DOI: 10.1042/BJ20082011


2008

24 Claridge, T. D. W.; Davies, S. G.; Polywka, M. E. C.; Roberts, P. M.; Russell, A. J.; Savory, E. D. and Smith, A. D. “Pure by NMR?” Org. Lett. 2008, 10, 5433–5436. DOI: 10.1021/ol802211p

23 Aciro, C.; Claridge, T. D. W.; Davies, S. G.; Roberts, P. M.; Russell, A. J. and Thomson, J. E. Ammonium directed dihydroxylation of 3-amino-cyclohex-1-enes: development of a metal-free dihydroxylation protocol. Org. Biomol. Chem. 2008, 20, 3751–3761. DOI: 10.1039/B808811J

22 Aciro, C.; Davies, S. G.; Roberts, P. M.; Russell, A. J.; Smith, A. D. and Thomson, J. E. Ammonium directed dihydroxylation: metal-free synthesis of the diastereoisomers of 3-amino-cyclohexane-1,2-diol. Org. Biomol. Chem. 2008, 20, 3762–3770. DOI: 10.1039/B808812H

21 Davies, S. G.; Mortimer, D. A. B.; Mulvaney, A. W.; Russell, A. J.; Skarphedinsson, H.; Smith A. D. and Vickers, R. J. An oxidatively-activated safety catch linker for solid phase synthesis. Org. Biomol. Chem., 2008, 6, 1625–1634. DOI: 10.1039/B802204F

20 Abraham, E.; Brock, E. A.; Candela-Lena, J. I.; Davies, S. G.; Georgiou, M.; Nicholson, R. L.; Perkins, J. H.; Roberts, P. M.; Russell, A. J.; Sánchez-Fernández, E. M.; Scott, P. M.; Smith, A. D. and Thomson, J. E. Asymmetric synthesis of N,O,O,O-tetra-acetyl D-lyxo-phytosphingosine, jaspine B (pachastrissamine), 2-epi-jaspine B, and deoxoprosophylline via lithium amide conjugate addition. Org. Biomol. Chem., 2008, 6, 1665–1673. DOI: 10.1039/B801671B

19 Abraham, E.; Candela-Lena, J. I.; Davies, S. G.; Georgiou, M.; Nicholson, R. L.; Roberts, P. M.; Russell, A. J.; Sanchez-Fernandez, E. M.; Smith, A. D.; Thomson, J. E. Asymmetric synthesis of N,O,O,O-tetra-acetyl D-lyxo-phytosphingosine, jaspine B (pachastrissamine) and its C(2)-epimer. Tetrahedron: Asymmetry 2008, 18, 2510–2513. DOI: https://doi.org/10.1016/j.tetasy.2007.10.026

18 Case-Green, S. C.; Davies, S. G.; Roberts, P. M.; Russell, A. J. and Thomson, J. A. Asymmetric synthesis of tetrahydrolipstatin and valilactone. Tetrahedron: Asymmetry, 2009, 19, 2870–2881. DOI: https://doi.org/10.1016/j.tetasy.2008.11.012

17 Claridge, T. D. W.; Davies, S. G.; Lee, J. A.; Nicholson, R. L.; Roberts, P. M.; Russell, A. J.; Smith, A. D. and Toms, S. M. Highly (E)-Selective Wadsworth-Emmons Reactions Promoted by Methylmagnesium Bromide. Org. Lett. 2008, 10, 5437–5440. DOI: 10.1021/ol802212e

16 Musameh, M. M.; Kachoosangi, R. T.; Xiao, L.; Russell, A. and Compton, R. G. Ionic liquid-carbon composite glucose biosensor. Biosensors and Bioelectronics, 2008, 24, 87–92. DOI: https://doi.org/10.1016/j.bios.2008.03.015

15 Abraham, E.; Davies, S. G.; Roberts, P. M.; Russell, A. J. and Thomson, J. E. Jaspine B (pachastrissamine) and 2-epi-jaspine B: synthesis and structural assignment. Tetrahedron: Asymmetry, 2008, 19, 1027–1047. DOI: https://doi.org/10.1016/j.tetasy.2008.04.017

14 Abraham, E.; Davies, S. G.; Docherty, A. J.; Ling, K. B.; Roberts, P. M.; Russell, A. J.; Thomson, J. E. and Toms, S. M. Parallel kinetic resolution of methyl (RS)-5-tris(phenylthio)methyl-cyclopent-1-ene-carboxylate for the asymmetric synthesis of (1R,2S,5S)- and (1S,2R,5R)-5-methyl-cispentacin. Tetrahedron: Asymmetry, 2008, 19, 1356–1362. DOI: https://doi.org/10.1016/j.tetasy.2008.05.016

13 Davies, S. G.; Durbin, M. J.; Hartman, S. J. S.; Matsuno, A.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Thomson, J. E. and Toms, S. M. Parallel kinetic resolution of tert-butyl (RS)-6-alkyl-cyclohex-1-ene-carboxylates for the asymmetric synthesis of 6-alkyl-substituted cishexacin derivatives. Tetrahedron: Asymmetry 2009, 19, 2870–2881. DOI: https://doi.org/10.1016/j.tetasy.2008.11.019

12 Aciro, C.; Davies, S. G.; Garner, A. C.; Ishii, Y.; Key, M. S.; Ling, K. B.; Prasad, R. S.; Roberts, P. M.; Rodriguez-Solla, H.; O’Leary-Steele, C.; Russell, A. J.; Sanganee, H. J.; Savory, E. D.; Smith, A. D. and Thomson, J. E. Stereoselective functionalisation of SuperQuat enamides: asymmetric synthesis of homochiral 1,2-diols and α-benzyloxy carbonyl compounds. Tetrahedron, 2008, 64, 9320–9344. DOI: https://doi.org/10.1016/j.tet.2008.07.012


2007

11 Cailleau, T.; Cooke, J. W. B.; Davies, S. G.; Ling, K. B.; Naylor, A.; Nicholson, R. L.; Price, P. D.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Thomson, J. E. Asymmetric synthesis of beta-amino-gamma-substituted-gamma-butyrolactones: double diastereoselective conjugate addition of homochiral lithium amides to homochiral alpha,beta-unsaturated esters. Org. Biomol. Chem. 2007, 5, 3922–3931. DOI: 10.1039/B712937H

10 Beddow, J. E.; Davies, S. G.; Ling, K. B.; Roberts, P. M.; Russell, A. J.; Smith, A. D.; Thomson, J. E. Asymmetric synthesis of beta(2)-amino acids: 2-substituted-3-aminopropanoic acids from N-acryloyl SuperQuat derivatives. Org. Biomol. Chem. 2007, 5, 2812–2825. DOI: 10.1039/B707689D

9 Davies, S. G.; Ling, K. B.; Roberts, P. M.; Russell, A. J.; Thomson, J. E. Diastereoselective Simmons-Smith cyclopropanations of allylic amines and carbamates. Chem. Commun. 2007, 39, 4029–4031. DOI: 10.1039/B711358G

8 Rogers, E. I.; Silvester, D. S.; Jones, S. E. W.; Aldous, L.; Hardacre, C.; Russell, A. J.; Davies, S. G.; Compton, R. G. Electrochemical kinetics of AgAg+ and TMPDTMPD+ in the room-temperature ionic liquid [C(4)mpyrr][NTf2]; toward optimizing reference electrodes for voltammetry in RTILs. J. Phys. Chem. C 2007, 111, 13957–13966. DOI: 10.1021/jp0737754

7 Davies, S. G.; Russell, A. J.; Sheppard, R. L.; Smith, A. D.; Thomson, J. E. Evaluating beta-amino acids as enantioselective organocatalysts of the Hajos-Parrish-Eder-Sauer-Wiechert reaction. Org. Biomol. Chem. 2007, 5, 3190–3200. DOI: 10.1039/B711171A

6 Madikane, V. E.; Bhakta, S.; Russell, A. J.; Campbell, W. E.; Claridge, T. D. W.; Elisha, B. G.; Davies, S. G.; Smith, P.; Sim, E. Inhibition of mycobacterial arylamine N-acetyltransferase contributes to anti-mycobacterial activity of Warburgia salutaris. Bioorg. Med. Chem. 2007, 15, 3579–3586. DOI: https://doi.org/10.1016/j.bmc.2007.02.011

5 Davies, S. G.; Mulvaney, A. W.; Russell, A. J.; Smith, A. D. Parallel synthesis of homochiral beta-amino acids. Tetrahedron: Asymmetry, 2007, 18, 1554–1566. DOI: https://doi.org/10.1016/j.tetasy.2007.06.008


pre-2007

4 Candela-Lena, J. I.; Davies, S. G.; Roberts, P. M.; Roux, B.; Russell, A. J.; Sanchez-Fernandez, E. M.; Smith, A. D. Asymmetric synthesis of alpha-mercapto-beta-amino acid derivatives: application to the synthesis of polysubstituted thiomorpholines. Tetrahedron: Asymmetry 2006, 17, 1135–1145. DOI: 10.1016/j.tetasy.2006.04.004

3 Davies, S. G.; Garrido, N. M.; Kruchinin, D.; Ichihara, O.; Kotchie, L. J.; Price, P. D.; Mortimer, A. J. P.; Russell, A. J.; Smith, A. D. Homochiral lithium amides for the asymmetric synthesis of beta-amino acids. Tetrahedron: Asymmetry, 2006, 17, 1793–1811. DOI: https://doi.org/10.1016/j.tetasy.2006.05.008

2 Westwood, I. M.; Kawamura, A.; Fullam, E.; Russell, A. J.; Davies, S. G.; Sim, E. Structure and mechanism of arylamine N-acetyltransferases. Curr. Top. Med. Chem. 2006, 6, 1641–1654. DOI: 10.2174/156802606778108979

1 Beddow, J. E.; Davies, S. G.; Smith, A. D.; Russell, A. J. Asymmetric synthesis of 2-alkyl- and 2-aryl-3-aminopropionic acids (beta(2)-amino acids) from (S)-N-acryloyl-5,5-dimethyloxazolidin-2-one SuperQuat derivatives. Chem. Commun. 2004, 23, 2778–2779. DOI: 10.1039/B410938D