| Year |
Citation |
Score |
| 2022 |
Buccini M, Tham L, Dhoro F, Skelton BW, Williams CM, Piggott MJ. Toward the Total Synthesis of Alpkinidine: Synthesis of Haloquinone CE Ring System Synthons and Attempted Nucleophilic Bisannulation. Acs Omega. 7: 19080-19092. PMID 35721899 DOI: 10.1021/acsomega.2c02116 |
0.304 |
|
| 2019 |
Sarkar MR, Houston SD, Savage GP, Williams CM, Krenske EH, Bell SG, De Voss JJ. Rearrangement-Free Hydroxylation of Methylcubanes by a Cytochrome P450: The Case for Dynamical Coupling of C-H Abstraction and Rebound. Journal of the American Chemical Society. PMID 31739667 DOI: 10.1021/Jacs.9B08064 |
0.547 |
|
| 2019 |
Houston SD, Fahrenhorst-Jones T, Xing H, Chalmers BA, Sykes ML, Stok JE, Farfan Soto C, Burns JM, Bernhardt PV, De Voss JJ, Boyle GM, Smith MT, Tsanaktsidis J, Savage GP, Avery VM, ... Williams CM, et al. The cubane paradigm in bioactive molecule discovery: further scope, limitations and the cyclooctatetraene complement. Organic & Biomolecular Chemistry. PMID 31241113 DOI: 10.1039/C9Ob01238A |
0.55 |
|
| 2019 |
Xing H, Houston SD, Chen X, Ghassabian S, Fahrenhorst-Jones T, Kuo A, Murray CP, Conn KA, Jaeschke KN, Jin DY, Pasay C, Bernhardt PV, Burns JM, Tsanaktsidis J, Savage GP, ... ... Williams CM, et al. Cyclooctatetraene: A Bioactive Cubane Paradigm Complement. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30681236 DOI: 10.1002/Chem.201806277 |
0.529 |
|
| 2018 |
Chalmers BA, Xing H, Houston S, Clark C, Ghassabian S, Kuo A, Cao B, Reitsma A, Murray CP, Stok JE, Boyle GM, Pierce CJ, Littler SW, Winkler DA, Bernhardt PV, ... ... Williams CM, et al. Corrigendum: Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere. Angewandte Chemie (International Ed. in English). 57: 8359. PMID 29975016 DOI: 10.1002/Anie.201711161 |
0.478 |
|
| 2017 |
San AT, Joyce DC, Hofman PJ, Macnish AJ, Webb RI, Matovic NJ, Williams CM, De Voss JJ, Wong SH, Smyth HE. Stable isotope dilution assay (SIDA) and HS-SPME-GCMS quantification of key aroma volatiles for fruit and sap of Australian mango cultivars. Food Chemistry. 221: 613-619. PMID 27979249 DOI: 10.1016/j.foodchem.2016.11.130 |
0.504 |
|
| 2016 |
Chalmers BA, Xing H, Houston S, Clark C, Ghassabian S, Kuo A, Cao B, Reitsma A, Murray CP, Stok JE, Boyle GM, Pierce CJ, Littler SW, Winkler DA, Bernhardt PV, ... ... Williams CM, et al. Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere. Angewandte Chemie (International Ed. in English). PMID 26846616 DOI: 10.1002/Anie.201510675 |
0.546 |
|
| 2016 |
Stok J, Chow S, Krenske E, Farfan Soto C, Matyas C, Poirier R, Williams C, De Voss JJ. Direct Observation of an Oxepin from a Bacterial Cytochrome P450 Catalyzed Oxidation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26811874 DOI: 10.1002/Chem.201600246 |
0.54 |
|
| 2010 |
ANG KH, PRAGER RH, WILLIAMS CM. ChemInform Abstract: The Chemistry of 5-Oxodihydroisoxazoles. Part 13. Reactions of the Imino Carbene Derived from Photolysis of Ethyl 5-Oxo-2-phenyl-2,5- dihydroisoxazole-4-carboxylate. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199529073 |
0.304 |
|
| 2009 |
Schwartz BD, Denton JR, Davies HM, Williams CM. Total Synthesis of (±)-Vibsanin E. Australian Journal of Chemistry. 62: 980-982. PMID 21297900 DOI: 10.1071/Ch09267 |
0.681 |
|
| 2009 |
Schwartz BD, Denton JR, Bernhardt PV, Davies HM, Williams CM. Towards the Total Synthesis of 3-Hydroxyvibsanin E. Synthesis. 2009: 2840-2846. PMID 20725592 DOI: 10.1055/S-0029-1216912 |
0.693 |
|
| 2009 |
Schwartz BD, Denton JR, Lian Y, Davies HM, Williams CM. Asymmetric [4 + 3] cycloadditions between vinylcarbenoids and dienes: application to the total synthesis of the natural product (-)-5-epi-vibsanin E. Journal of the American Chemical Society. 131: 8329-32. PMID 19445507 DOI: 10.1021/Ja9019484 |
0.711 |
|
| 2009 |
Davies H, Williams C, Schwartz B, Denton J, Lian Y. Synthesis of (-)-5-epi-Vibsanin E Synfacts. 2009: 1312-1312. DOI: 10.1055/S-0029-1218334 |
0.685 |
|
| 2009 |
Schwartz BD, Porzelle A, Jack KS, Faber JM, Gentle IR, Williams CM. Cyclic enones as substrates in the Morita-Baylis-Hillman reaction: Surfactant interactions, scope and scalability with an emphasis on formaldehyde Advanced Synthesis and Catalysis. 351: 1148-1154. DOI: 10.1002/adsc.200800739 |
0.655 |
|
| 2008 |
Schwartz BD, Williams CM, Bernhardt PV. End game strategies towards the total synthesis of vibsanin E, 3-hydroxyvibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A. Beilstein Journal of Organic Chemistry. 4: 34. PMID 18982074 DOI: 10.3762/bjoc.4.34 |
0.675 |
|
| 2008 |
Schwartz BD, Williams CM, Anders E, Bernhardt PV. Exploiting the Anders-Gaßner variant on the Wittig reaction: new methodology for the synthesis of 3,3-dimethylacroyl enol esters Tetrahedron. 64: 6482-6487. DOI: 10.1016/j.tet.2008.04.068 |
0.698 |
|
| 2008 |
Schwartz BD, Williams CM, Anders E, Bernhardt PV. ChemInform Abstract: Exploiting the Anders-Gassner Variant on the Wittig Reaction: New Methodology for the Synthesis of 3,3-Dimethylacroyl Enol Esters. Cheminform. 39. DOI: 10.1002/CHIN.200846053 |
0.697 |
|
| 2006 |
Schwartz BD, Tilly DP, Heim R, Wiedemann S, Williams CM, Bernhardt PV. 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. 3181-3192. DOI: 10.1002/ejoc.200600246 |
0.65 |
|
| 2006 |
Porzelle A, Williams CM, Schwartz BD, Gentle IR. Evaluating the Baylis—Hillman Reaction of Cyclic Enones Using Surfactants in Water. Cheminform. 37. DOI: 10.1002/chin.200615063 |
0.656 |
|
| 2005 |
Porzelle A, Williams CM, Schwartz BD, Gentle IR. Evaluating the Baylis-Hillman reaction of cyclic enones using surfactants in water Synlett. 2923-2926. DOI: 10.1055/s-2005-921890 |
0.657 |
|
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