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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