By Associate Professor Luke Hunter

Journal articles

Hunter L; Condie GC; Harding MM, 2011, 'ChemInform Abstract: Reversible Aqueous Metathesis Reactions for Potential Application in Dynamic Combinatorial Chemistry.', ChemInform, 42, http://dx.doi.org/10.1002/chin.201102054

Hunter L; Jolliffe KA; Jordan M; Jensen P; Macquart R, 2011, 'Synthesis and Conformational Analysis of á,â-Difluoro-ã-amino Acid Derivatives', Chemistry - a European Journal, 17, pp. 2340 - 2343, http://dx.doi.org/10.1002/chem.201003320

Hunter L; Chung J, 2011, 'Total synthesis of unguisin A', Journal of Organic Chemistry, 76, pp. 5502 - 5505, http://dx.doi.org/10.1021/jo200813a

Hunter L, 2010, 'ChemInform Abstract: The C‐F— Bond as a Conformational Tool in Organic and Biological Chemistry', ChemInform, 41, http://dx.doi.org/10.1002/chin.201041259

Hunter L; Condie G; Harding MM, 2010, 'Reversible aqueous metathesis reactions for potential application in dynamic combinatorial chemistry', Tetrahedron Letters, 51, pp. 5064 - 5067, http://dx.doi.org/10.1016/j.tetlet.2010.07.105

Hunter L, 2010, 'The C-F bond as a conformational tool in organic and biomolecular chemistry', Beilstein Journal of Organic Chemistry, 6, http://dx.doi.org/10.3762/bjoc.6.38

Hunter L; Kirsch P; Slawin AMZ; O'Hagan D, 2009, 'Synthesis and Structure of Stereoisomeric Multivicinal Hexafluoroalkanes', Angewandte Chemie, 121, pp. 5565 - 5568, http://dx.doi.org/10.1002/ange.200901956

Hunter L; Kirsch P; Slawin AMZ; O'Hagan D, 2009, 'Synthesis and Structure of Stereoisomeric Multivicinal Hexafluoroalkanes.', Angew. Chem., Int. Ed., 48, pp. 5457 - S5457/63, http://dx.doi.org/10.1002/anie.200901956

Hunter L; O'Hagan D, 2008, 'ChemInform Abstract: Multi‐vicinal Fluoroalkanes: A New Class of Organofluorine Compounds', ChemInform, 39, http://dx.doi.org/10.1002/chin.200847242

Hunter L; O'Hagan D, 2008, 'Multi-vicinal fluoroalkanes: a new class of organofluorine compounds.', Org. Biomol. Chem., 6, pp. 2843 - 2848, http://dx.doi.org/10.1039/b809432b

Hunter L; Kirsch P; Hamilton JTG; O'Hagan D, 2008, 'The multi-vicinal fluoroalkane motif: an examination of 2,3,4,5-tetrafluorohexane stereoisomers.', Org. Biomol. Chem., 6, pp. 3105 - 3108, http://dx.doi.org/10.1039/b807449f

Hunter L; Slawin AMZ; Kirsch P; O'Hagan D, 2007, 'Synthesis and Conformation of Multi‐Vicinal Fluoroalkane Diastereoisomers', Angewandte Chemie, 119, pp. 8033 - 8036, http://dx.doi.org/10.1002/ange.200701988

Hunter L; Slawin AMZ; Kirsch P; O'Hagan D, 2007, 'Synthesis and conformation of multi-vicinal fluoroalkane diastereoisomers.', Angew. Chem., Int. Ed., 46, pp. 7887 - 7890, http://dx.doi.org/10.1002/anie.200701988

Hunter L; O'Hagan D; Slawin AMZ, 2006, 'Enantioselective synthesis of an all-syn four vicinal fluorine motif', Journal of the American Chemical Society, 128, pp. 16422 - 16423, http://dx.doi.org/10.1021/ja066188p

Hunter L; McLeod MD; Hutton CA, 2005, 'Synthesis of the β‐Hydroxydopa—y‐Hydroxy‐δ‐sulfinylnorvaline (I) Component of Ustiloxins A and B (II).', ChemInform, 36, http://dx.doi.org/10.1002/chin.200533223

Hunter L; McLeod MD; Hutton CA, 2005, 'Synthesis of the β-hydroxydopa-γ-hydroxy-δ-sulfinylnorvaline component of ustiloxins A and B.', Org. Biomol. Chem., 3, pp. 732 - 734, http://dx.doi.org/10.1039/b418876d

Hutchins LM; Hunter L; Ehya N; Gibbs MD; Bergquist PL; Hutton CA, 2004, 'Highly enantioselective recombinant thermoalkalophilic lipases from Geobacillus and Bacillus sp', Tetrahedron Asymmetry, 15, pp. 2975 - 2980, http://dx.doi.org/10.1016/j.tetasy.2004.07.041

Hunter L; Hutton CA, 2004, 'Preparation of Selectively Protected L‐Dopa Derivatives: Oxidation of Tyrosine‐3‐boronates.', ChemInform, 35, http://dx.doi.org/10.1002/chin.200412210

Hunter L; Hutton CA, 2003, 'Preparation of Selectively Protected L-DOPA Derivatives: Oxidation of Tyrosine-3-boronates.', Aust. J. Chem., 56, pp. 1095 - 1098, http://dx.doi.org/10.1071/CH03181

Sunna A; Hunter L; Hutton CA; Bergquist PL, 2002, 'Biochemical characterization of a recombinant thermoalkalophilic lipase and assessment of its substrate enantioselectivity.', Enzyme Microb. Technol., 31, pp. 472 - 476, http://dx.doi.org/10.1016/S0141-0229(02)00133-3

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