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2006 Journal Article Azedaralide: total synthesis, relative and absolute stereochemical assignmentBaker, L. A., Williams, C. M., Bernhardt, P. V. and Yanik, G. W. (2006). Azedaralide: total synthesis, relative and absolute stereochemical assignment. Tetrahedron, 62 (31), 7355-7360. doi: 10.1016/j.tet.2006.05.030 |
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2006 Journal Article o-iodoxybenzoic acid (IBX): pK(a) and proton-affinity analysisGallen, Michael J., Goummont, Regis, Clark, Timothy, Terrier, Francois and Williams, Craig M. (2006). o-iodoxybenzoic acid (IBX): pK(a) and proton-affinity analysis. Angewandte Chemie-international Edition, 45 (18), 2929-2934. doi: 10.1002/anie.200504156 |
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2006 Journal Article Towards the total synthesis of vibsanin E, 15-O-methylcyclovibsanin B, 3-hydroxyvibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin ASchwartz, B. D., Tilly, D. P., Heim, R., Wiedemann, S., Williams, C. M. and Bernhardt, P. V. (2006). Towards the total synthesis of vibsanin E, 15-O-methylcyclovibsanin B, 3-hydroxyvibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A. European Journal of Organic Chemistry, 2006 (14), 3181-3192. doi: 10.1002/ejoc.200600246 |
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2005 Journal Article Investigating direct routes to an advanced intermediate for the synthesis of C-20 diterpene alkaloidsWilliams, C. M., Mander, L. N., Bernhardt, P. V. and Willis, A. C. (2005). Investigating direct routes to an advanced intermediate for the synthesis of C-20 diterpene alkaloids. Tetrahedron, 61 (15), 3759-3769. doi: 10.1016/j.tet.2005.02.014 |
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2005 Journal Article Evaluating the Baylis-Hillman reaction of cyclic enones using surfactants in waterPorzelle, A., Williams, C. M., Schwartz, B. D. and Gentle, I. R. (2005). Evaluating the Baylis-Hillman reaction of cyclic enones using surfactants in water. Synlett, 19 (19) D25505ST, 2923-2926. doi: 10.1055/s-2005-921890 |
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2005 Book Chapter Product Class 10: Acridin-9(10H)-ones and Related SystemsPrager, R.H. and Williams, C.M. (2005). Product Class 10: Acridin-9(10H)-ones and Related Systems. Science of Synthesis: Category 2, Hetarenes and Related Ring Systems. (pp. 1029-1064) edited by Black, D. StC.. New York: Thieme. doi: 10.1055/sos-SD-015-01714 |
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2005 Journal Article "One-Step" alkynylation of adamantyl iodide with Silver(I) acetylidesPouwer, R. H., Williams, C. M., Raine, A. L. and Harper, J. B. (2005). "One-Step" alkynylation of adamantyl iodide with Silver(I) acetylides. Organic Letters, 7 (7), 1323-1325. doi: 10.1021/ol050121+ |
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2005 Journal Article Nitrogen is a requirement for the photochemical induced 3-azabicyclo[3.3.1]nonane skeletal rearrangement!Williams, C. M., Heim, R. and Bernhardt, P. V. (2005). Nitrogen is a requirement for the photochemical induced 3-azabicyclo[3.3.1]nonane skeletal rearrangement!. Tetrahedron, 61 (15), 3771-3779. doi: 10.1016/j.tet.2005.02.013 |
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2005 Journal Article Expedient construction of the vibsanin E core without the use of protecting groupsHeim, Ralf, Wiedemann, Stefan, Williams, Craig M. and Bernhardt, Paul V. (2005). Expedient construction of the vibsanin E core without the use of protecting groups. Organic Letters, 7 (7), 1327-1329. doi: 10.1021/ol0501222 |
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2005 Journal Article Construction of the cyclovibsanin core via a biogenetically modeled approachTilly, David P., Williams, Craig M. and Bernhardt, Paul V. (2005). Construction of the cyclovibsanin core via a biogenetically modeled approach. Organic Letters, 7 (23), 5155-5157. doi: 10.1021/ol051897d |
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2005 Book Chapter Product Class 9: AcridinesPrager, R.H. and Williams, C.M. (2005). Product Class 9: Acridines. Science of Synthesis: Category 2, Hetarenes and Related Ring Systems. (pp. 987-1028) edited by Black, D. StC.. New York: Thieme. doi: 10.1055/sos-SD-015-01674 |
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2004 Journal Article Guaiacol transprotection: replacement of the phenoxy isopropyl protecting function by acetylWilliams, Craig M. and Mander, Lewis N. (2004). Guaiacol transprotection: replacement of the phenoxy isopropyl protecting function by acetyl. Tetrahedron Letters, 45 (4), 667-669. doi: 10.1016/j.tetlet.2003.11.065 |
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2004 Journal Article Unprecedented photochemical induced cascading rearrangement of the 3-azabicyclo[3.3.1] nonane skeletonWilliams, Craig M., Heim, Ralf, Brecknell, Douglas J. and Bernhardt, Paul V. (2004). Unprecedented photochemical induced cascading rearrangement of the 3-azabicyclo[3.3.1] nonane skeleton. Organic and Biomolecular Chemistry, 2 (6), 806-807. doi: 10.1039/b402200a |
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2003 Journal Article The synthesis and X-ray crystal structure of 9-carboxyhexahydro-7-methoxy-4a,7-ethano-benzopyran-5-en-1-oneWilliams, C. M., Bernhardt, P. V., Wiedemann, S. and Barden, M. C. (2003). The synthesis and X-ray crystal structure of 9-carboxyhexahydro-7-methoxy-4a,7-ethano-benzopyran-5-en-1-one. Journal of Chemical Research (S), 12 (12), 784-785. doi: 10.3184/030823403322840387 |
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2003 Other Outputs Compositions comprising nitric oxide donors and opioid analgesicsSmith, M. T., Brown, L. C., Harvey, M. and Williams, C. M. (2003). Compositions comprising nitric oxide donors and opioid analgesics. PCT/AU03/00335. |
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2003 Journal Article 1-Ethynyl-2-isopropoxy-3-methoxybenzeneWilliams, Craig M., Mander, Lewis N. and Bernhardt, Paul V. (2003). 1-Ethynyl-2-isopropoxy-3-methoxybenzene. Acta Crystallographica Section E, 59 (4), 0561-0563. doi: 10.1107/S1600536803006585 |
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2003 Journal Article Synthesis of novel 2-amino-1,3-thiazole-5-carboxylates utilising ultrasonic and thermally mediated aminolysisBaker, L. A. and Williams, C. M. (2003). Synthesis of novel 2-amino-1,3-thiazole-5-carboxylates utilising ultrasonic and thermally mediated aminolysis. Journal of Heterocyclic Chemistry, 40 (2), 353-356. doi: 10.1002/jhet.5570400225 |
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2003 Journal Article Oxidative degradation of benzene ringsMander, L. N. and Williams, C. M. (2003). Oxidative degradation of benzene rings. Tetrahedron, 59 (8), 1105-1136. doi: 10.1016/S0040-4020(02)01492-8 |
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2003 Journal Article The synthesis and X-ray crystal structure of 6-bromo-2,4,4-trimethyl-cyclohex-2-enoneWilliams, C. M. and Bernhardt, P. V. (2003). The synthesis and X-ray crystal structure of 6-bromo-2,4,4-trimethyl-cyclohex-2-enone. Journal of Chemical Research-s, 2003 (7), 410-411. doi: 10.3184/030823403103174326 |
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2003 Journal Article Bridgehead arylation: A direct route to advanced intermediates for the synthesis of C-20 diterpene alkaloidsWilliams, C. M. and Mander, L. N. (2003). Bridgehead arylation: A direct route to advanced intermediates for the synthesis of C-20 diterpene alkaloids. Organic Letters, 5 (19), 3499-3502. doi: 10.1021/ol0353060 |
