Publications from Pharmacat projects:

1. "Clarification of the role of water in proline-mediated aldol reactions", N. Zotova, A. Franzke, A. Armstrong and D.G. Blackmond, J. Am. Chem. Soc., 2007129, 15100. DOI: 10.1021/ja0738881

2. "Kinetic and Mechanistic Studies of Proline-Mediated Direct Intermolecular Aldol Reactions", N. Zotova, L. J. Broadbelt, A. Armstrong, and D.G. Blackmond, Bioorg. Med. Chem. Lett., 200919, 3934. DOI: 10.1016/j.bmcl.2009.03.112

3. "A Coherent Mechanistic Rationale for Additive Effects and Autoinductive Behavior in Proline-Mediated Reactions", N. Zotova, A. Moran, A. Armstrong, and D. G. Blackmond, Adv. Synth. Catal.2009351, 2765. DOI: 10.1002/adsc.200900665

4. “Catalysis in Flow: Practical and Selective Aerobic Oxidation of Alcohols”, N. Zotova, K. Hellgardt, G. H. Kelsall, A. S. Jessiman and K. K. Hii, Green Chem., 201012, 2157-2163. DOI: 10.1039/c0gc00493f

5. “Catalysis in Flow: Au-Catalysed Alkylation of Amines by Alcohols”, N. Zotova, F. J. Roberts, G. H. Kelsall, A. S. Jessiman, K. Hellgardt, and K. K. Hii, Green Chem., 201214, 226. DOI:10.1039/c1gc16118k

6. “Speciation of Pd(OAc)2 in Ligandless Suzuki-Miyaura Reactions”, L. A. Adrio, B. N. Nguyen, G. Guilera, A. G. Livingston and K. K. Hii, Cat. Sci. Tech., 20122, 316. DOI: 10.1039/c1cy00241d

7. "Catalysis in flow: Operando study of Pd catalyst speciation and leaching", J. B. Brazier, B. N. Nguyen, L. A. Adrio, E. M. Barreiro, W. P. Leong, M. A. Newton, S. J. A. Figueroa, K. Hellgardt and K. K. Hii, Catalysis Today2014229, 95. DOI: 10.1016/j.cattod.2013.10.079.

8. "Fabrication of hybrid polymer/metal organic framework membranes: mixed matrix membranesversus in situ growth", J. Campbell, G. Szekely, R. P. Davies, D. C. Braddock and A. G, Livingston, J. Mater. Chem. A, 20142, 9260-9271. DOI: 10.1039/C4TA00628C

9. "Controlling Crystallization via Organic Solvent Nanofiltration: The Influence of Flux on Griseofulvin Crystallization", J. Campbell, L. G. Peeva and A. G. Livingston, Cryst. Growth Des., 201414, 192–2200. DOI: 10.1021/cg401708s

10. "Metal-Free Hydrogenation Catalyzed by an Air-Stable Borane: Use of Solvent as a Frustrated Lewis Base", D. J. Scott, M. J. Fuchter and A. E. Ashley, Angew. Chem. Int. Ed. 201453, 10218-10222. DOI: 10.1002/anie.201405531

11. "Nonmetal Catalyzed Hydrogenation of Cabonyl Compounds", D. J. Scott, M. J. Fuchter and A. E. Ashley, J. Am. Chem. Soc.2014, 136, 15813–15816. DOI: 10.1021/ja5088979

12. "Chemo- and Diasteroselectivities in the Electrochemical Reduction of Maleimides", K. Rix, G. H. Kelsall, K. Hellgardt and K. K. Hii, ChemSusChem, 2015, 8, 665  671 DOI: 10.1002/cssc.201403184

13. "Synthesis, Characterisation and Reactivity of Copper(I) Amide Complexes and Studies on their Role in the Modified Ullmann Amination Reaction", S. Sung, D. C. Braddock, A. Armstrong, C. Brennan, D. Sale, A. J. P. White, and R. P. Davies, Chem. Eur. J., 2015, 21, 7179-7192. DOI: 10.1002/chem.201405699

14. “Operando XAFS of supported Pd nanoparticles in flowing ethanol/water mixtures: implications for greener catalysis”, M. A. Newton, J. B. Brazier, E. M. Barreiro, C. J. Mulligan, S. Parry, H. Emmerich, L. A. Adrio, K. Hellgardt and K. K. Hii, Green Chemistry, Green Chem. 2016, 18, 406-411. DOI: 10.1039/c5gc01600b.

15. “Electronic structures of cyclometalated palladium complexes in the higher oxidation states”, B. N. Nguyen, L. A. Adrio, T. Albrecht, A. J. P. White, M. A. Newton, M. Nachtegaal, S. J. A. Figueroa, and K. K. Hii, Dalton Trans., 201544, 16586 – 16591. DOI: 10.1039/c5dt02104a

16. “Facile Protocol for Water-Tolerant "Frustrated Lewis Pair"-Catalyzed Hydrogenation”, D. J. Scott, T. R. Simmons, E. J. Lawreance, G. G> Wildgoose, M. J. Fuchter and A. E. Ashley, ACS Catal., 2015, 5, 5540-5544. DOI: 10.1021/acscatal.5b01417