Bill C. Hawkins, Ph.D - Publications

Affiliations: 
2012- Chemistry University of Otago, Dunedin, Otago, New Zealand 
Area:
Total Synthesis, Organic Chemistry

34 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Craig AJ, Cording AP, Garden AL, Hawkins BC. Does the Reaction of Cyclopropyl Acid Chlorides and Imines To Form 1,3-Oxazin-4-enone Heterocycles Proceed via a Ketene or an -Acyl-iminium Mechanism? The Journal of Organic Chemistry. PMID 32207973 DOI: 10.1021/Acs.Joc.0C00229  0.336
2020 Swaney B, Luxenburger A, Lucas NT, Hawkins BC, Hinkley SF. The synthesis of 3-azabicyclo[4.3.0]nonane scaffolds from brefeldin A Tetrahedron Letters. 61: 152006. DOI: 10.1016/J.Tetlet.2020.152006  0.474
2019 Hamiaux C, Larsen L, Lee HW, Luo Z, Sharma P, Hawkins BC, Perry NB, Snowden KC. Chemical synthesis and characterization of a new quinazolinedione competitive antagonist for strigolactone receptors with an unexpected binding mode. The Biochemical Journal. PMID 31186286 DOI: 10.1042/Bcj20190288  0.333
2019 Gai S, Lucas NT, Hawkins BC. Benzannulated 6,5-Spiroketals from Donor-Acceptor Cyclopropanes. Organic Letters. PMID 30924665 DOI: 10.1021/Acs.Orglett.9B00878  0.443
2019 Craig AJ, Hawkins BC. The Bonding and Reactivity of α-Carbonyl Cyclopropanes Synthesis. 52: 27-39. DOI: 10.1055/S-0039-1690695  0.362
2019 Smith RJ, Hawkins BC. Synthetic Strategies towards the Synthesis of Oxyisocyclointegrin European Journal of Organic Chemistry. 2019: 6847-6854. DOI: 10.1002/Ejoc.201901294  0.44
2018 Swaney B, Gai S, Clark M, Hawkins BC. Selective mono-allylation of 1,3-diketones and their use in the synthesis of 3-allyl chromones and benzannulated 6,5-bicyclic ketals. Chemistry, An Asian Journal. PMID 30552751 DOI: 10.1002/Asia.201801695  0.496
2018 Lamb RA, Lucas NT, Lessene G, Hawkins BC. Strategies, Setbacks and Successes in the Synthesis of (-)-Spiroleucettadine. The Journal of Organic Chemistry. PMID 30003773 DOI: 10.1021/Acs.Joc.8B01404  0.456
2018 Lamb R, Lessene G, Hawkins B. The Synthesis of (–)-Spiroleucettadine Synlett. 29: 1125-1130. DOI: 10.1055/S-0036-1591776  0.38
2018 French SA, Clark MR, Smith RJ, Brind T, Hawkins BC. Expedient synthesis of xanthones and multi-functionalized chromones from 1,1-diacyl cyclopropanes Tetrahedron. 74: 5340-5350. DOI: 10.1016/J.Tet.2018.04.003  0.512
2017 Hawkins BC, Lamb R, Aberle N, Lucas N, Lessene G. Total Synthesis of (-)-Spiroleucettadine. Angewandte Chemie (International Ed. in English). PMID 28960638 DOI: 10.1002/Anie.201708110  0.474
2017 Smith RJ, Nhu D, Clark MR, Gai S, Lucas NT, Hawkins BC. Synthesis of Chromones from 1,1-Diacylcyclopropanes: Towards the Synthesis of Bromophycoic Acid E. The Journal of Organic Chemistry. PMID 28440639 DOI: 10.1021/Acs.Joc.7B00648  0.46
2017 Nhu D, Larsen L, Perry NB, Larsen DS, Hawkins BC. Sweet Poisons: Synthetic Strategies towards Tutin Glycosides Australian Journal of Chemistry. 70: 301. DOI: 10.1071/Ch16429  0.351
2017 Hawkins B, Craig A. Metal-Free Synthesis of Oxazinones and Their Reductive Ring Opening to Provide Cyclopropyl Carbinols Synthesis. 49: 1955-1968. DOI: 10.1055/S-0036-1588748  0.462
2016 Smith RJ, Mills DA, Nhu D, Tan EW, Lucas NT, Hawkins BC. The Synthesis of Multi-Functionalized 1,3-Oxazin-4-ones from Donor-Acceptor Cyclopropanes. The Journal of Organic Chemistry. PMID 26867102 DOI: 10.1021/Acs.Joc.6B00112  0.45
2016 Badart MP, Squires CM, Baird SK, Hawkins BC. The synthesis of clavatadine C Tetrahedron Letters. 57: 5108-5111. DOI: 10.1016/J.Tetlet.2016.10.019  0.453
2015 Lei J, Burgess EJ, Richardson AT, Hawkins BC, Baird SK, Smallfield BM, van Klink JW, Perry NB. Cytotoxic Amides from Fruits of Kawakawa, Macropiper excelsum. Planta Medica. 81: 1163-8. PMID 26039266 DOI: 10.1055/S-0035-1546106  0.359
2015 Revalde JL, Li Y, Hawkins BC, Rosengren RJ, Paxton JW. Heterocyclic cyclohexanone monocarbonyl analogs of curcumin can inhibit the activity of ATP-binding cassette transporters in cancer multidrug resistance Biochemical Pharmacology. 93: 305-317. PMID 25543853 DOI: 10.1016/J.Bcp.2014.12.012  0.328
2015 Craig AJ, van der Salm L, Stevens-Cullinane L, Lucas NT, Tan EW, Hawkins BC. Expedient metal-free synthesis of 1,3-oxazinen-4-ones. Organic Letters. 17: 234-7. PMID 25537108 DOI: 10.1021/Ol503350H  0.415
2015 Lamb RA, Badart MP, Swaney BE, Gai S, Baird SK, Hawkins BC. The Synthesis and Biological Evaluation of Anithiactin A/Thiasporine C and Analogues Australian Journal of Chemistry. 68: 1829-1833. DOI: 10.1071/Ch15461  0.45
2015 Nhu D, Hawkins BC, Burns CJ. Phase transfer catalysis extends the scope of the Algar-Flynn-Oyamada synthesis of 3-Hydroxyflavones Australian Journal of Chemistry. 68: 1102-1107. DOI: 10.1071/Ch14620  0.385
2014 Hawkins BC, Lindqvist LM, Nhu D, Sharp PP, Segal D, Powell AK, Campbell M, Ryan E, Chambers JM, White JM, Rizzacasa MA, Lessene G, Huang DC, Burns CJ. Simplified silvestrol analogues with potent cytotoxic activity. Chemmedchem. 9: 1556-66. PMID 24677741 DOI: 10.1002/Cmdc.201400024  0.584
2014 Stevens-Cullinane L, Lucas NT, Hawkins BC. Sterically controlled diels-alder cycloadditions: Rapid entry into the illudin scaffold European Journal of Organic Chemistry. 2014: 4767-4772. DOI: 10.1002/Ejoc.201402461  0.44
2013 Birkett S, Ganame D, Hawkins BC, Meiries S, Quach T, Rizzacasa MA. Total synthesis of the proposed structure of 8-deshydroxyajudazol A: a modified approach to 2,4-disubstituted oxazoles. The Journal of Organic Chemistry. 78: 116-23. PMID 23126596 DOI: 10.1021/Jo302055W  0.641
2012 Hawkins B, Paddock VL, Tölle N, Zard SZ. A convenient conversion of terminal alkenes into homologous unsaturated and doubly unsaturated esters. Organic Letters. 14: 1020-3. PMID 22296044 DOI: 10.1021/Ol203387R  0.513
2012 Hawkins B, Paddock VL, Tölle N, Zard SZ. A convenient conversion of terminal alkenes into homologous unsaturated and doubly unsaturated esters Organic Letters. 14: 1020-1023. DOI: 10.1021/ol203387r  0.484
2012 Hawkins B, Paddock VL, Toelle N, Zard SZ. ChemInform Abstract: A Convenient Conversion of Terminal Alkenes into Homologous Unsaturated and Doubly Unsaturated Esters. Cheminform. 43: no-no. DOI: 10.1002/chin.201225078  0.307
2011 Birkett S, Ganame D, Hawkins BC, Meiries S, Quach T, Rizzacasa MA. Total synthesis of 8-deshydroxyajudazol B. Organic Letters. 13: 1964-7. PMID 21410165 DOI: 10.1021/Ol200331U  0.63
2009 Adams TE, El Sous M, Hawkins BC, Hirner S, Holloway G, Khoo ML, Owen DJ, Savage GP, Scammells PJ, Rizzacasa MA. Total synthesis of the potent anticancer Aglaia metabolites (-)-silvestrol and (-)-episilvestrol and the active analogue (-)-4'-desmethoxyepisilvestrol. Journal of the American Chemical Society. 131: 1607-16. PMID 19140688 DOI: 10.1021/Ja808402E  0.642
2008 Thayumanavan R, Hawkins BC, Keller PA, Pyne SG, Ball GE. A mild and general method for the synthesis of 5-substituted and 5,5-disubstituted fulleroprolines. Organic Letters. 10: 1315-7. PMID 18288860 DOI: 10.1021/Ol8002157  0.497
2007 Hawkins BC, Keller PA, Pyne SG. Reductive ring opening reactions of diphenyldihydrofullerenylpyrroles Tetrahedron Letters. 48: 7533-7536. DOI: 10.1016/J.Tetlet.2007.08.044  0.417
2006 Keller PA, Pyne SG, Hawkins BC. Reactions of iminoglycines with C60 fullerene and their unambiguous characterisation using NMR spectroscopy Comptes Rendus Chimie. 9: 1100-1106. DOI: 10.1016/J.Crci.2006.01.002  0.394
2005 Ball GE, Burley GA, Chaker L, Hawkins BC, Williams JR, Keller PA, Pyne SG. Structural reassignment of the mono- and bis-addition products from the addition reactions of N-(Diphenylmethylene)glycinate esters to [60]fullerene under Bingel conditions. The Journal of Organic Chemistry. 70: 8572-4. PMID 16209611 DOI: 10.1021/Jo051282U  0.396
2005 Chaker L, Ball GE, Williams JR, Burley GA, Hawkins BC, Keller PA, Pyne SG. Regioselective synthesis of novel e-edge-[60] fullerenylmethanodihydropyrroles and 1,2-dihydromethano[60]fullerenes European Journal of Organic Chemistry. 5158-5162. DOI: 10.1002/Ejoc.200500694  0.435
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