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2019

Journal Article

Thermal and sensitiveness determination of cubanes: towards cubane‐based fuels for infrared countermeasures

Dallaston, Madeleine A., Brusnahan, Jason S., Wall, Craig and Williams, Craig M. (2019). Thermal and sensitiveness determination of cubanes: towards cubane‐based fuels for infrared countermeasures. Chemistry: A European Journal, 25 (35) chem.201901086, 8344-8352. doi: 10.1002/chem.201901086

Thermal and sensitiveness determination of cubanes: towards cubane‐based fuels for infrared countermeasures

2019

Journal Article

Reassignments and corroborations of oxo-bridged natural products directed by OSE and DU8+ NMR computation

Kutateladze, Andrei G., Krenske, Elizabeth H. and Williams, Craig M. (2019). Reassignments and corroborations of oxo-bridged natural products directed by OSE and DU8+ NMR computation. Angewandte Chemie International Edition, 58 (21), 7107-7112. doi: 10.1002/anie.201902777

Reassignments and corroborations of oxo-bridged natural products directed by OSE and DU8+ NMR computation

2019

Journal Article

Determining the necessity of phenyl ring π-character in warfarin

Xing, Hui, Houston, Sevan D., Chen, Xuejie, Jin, Da-Yun, Savage, G. Paul, Tie, Jian-Ke and Williams, Craig M. (2019). Determining the necessity of phenyl ring π-character in warfarin. Bioorganic and Medicinal Chemistry Letters, 29 (15), 1954-1956. doi: 10.1016/j.bmcl.2019.05.039

Determining the necessity of phenyl ring π-character in warfarin

2019

Journal Article

Nitric oxide modulates μ‐opioid receptor function in vitro

Huang, Lillian, Wyse, Bruce D., Williams, Craig M. and Smith, Maree T. (2019). Nitric oxide modulates μ‐opioid receptor function in vitro. Clinical and Experimental Pharmacology and Physiology, 46 (7) 1440-1681.13091, 676-685. doi: 10.1111/1440-1681.13091

Nitric oxide modulates μ‐opioid receptor function in vitro

2019

Journal Article

Stachyonic acid: a dengue virus inhibitor from Basilicum polystachyon

Tan, Yuen P., Houston, Sevan D., Modhiran, Naphak, Savchenko, Andrei I., Boyle, Glen M., Young, Paul R., Watterson, Daniel and Williams, Craig M. (2019). Stachyonic acid: a dengue virus inhibitor from Basilicum polystachyon. Chemistry – A European Journal, 25 (22) chem.201900591, 5664-5667. doi: 10.1002/chem.201900591

Stachyonic acid: a dengue virus inhibitor from Basilicum polystachyon

2019

Journal Article

Cyclooctatetraenes through valence isomerization of cubanes: scope and limitations

Houston, Sevan D., Xing, Hui, Bernhardt, Paul V., Vanden Berg, Timothy J., Tsanaktsidis, John, Savage, G. Paul and Williams, Craig M. (2019). Cyclooctatetraenes through valence isomerization of cubanes: scope and limitations. Chemistry: A European Journal, 25 (11), 2735-2739. doi: 10.1002/chem.201805124

Cyclooctatetraenes through valence isomerization of cubanes: scope and limitations

2019

Journal Article

Cyclooctatetraene: a bioactive cubane paradigm complement

Xing, Hui, Houston, Sevan D., Chen, Xuejie, Ghassabian, Sussan, Fahrenhorst-Jones, Tyler, Kuo, Andy, Murray, Cody-Ellen P., Conn, Kyna-Anne, Jaeschke, Kara N., Jin, Da-Yun, Pasay, Cielo, Bernhardt, Paul V., Burns, Jed M., Tsanaktsidis, John, Savage, G. Paul, Boyle, Glen M., De Voss, James J., McCarthy, James, Walter, Gimme H., Burne, Thomas H. J., Smith, Maree T., Tie, Jian-Ke and Williams, Craig M. (2019). Cyclooctatetraene: a bioactive cubane paradigm complement. Chemistry: A European Journal, 25 (11), 2729-2734. doi: 10.1002/chem.201806277

Cyclooctatetraene: a bioactive cubane paradigm complement

2019

Journal Article

Cubanes in medicinal chemistry

Reekie, Tristan A., Williams, Craig M., Rendina, Louis M. and Kassiou, Michael (2019). Cubanes in medicinal chemistry. Journal of Medicinal Chemistry, 62 (3) acs.jmedchem.8b00888, 1078-1095. doi: 10.1021/acs.jmedchem.8b00888

Cubanes in medicinal chemistry

2019

Journal Article

New Halimanes from the Australian rainforest plant Croton Insularis

Maslovskaya, Lidia A., Savchenko, Andrei I., Gordon, Victoria A., Reddell, Paul W., Pierce, Carly J., Boyle, Glen M., Parsons, Peter G. and Williams, Craig M. (2019). New Halimanes from the Australian rainforest plant Croton Insularis. European Journal of Organic Chemistry, 2019 (5), 1058-1060. doi: 10.1002/ejoc.201801548

New Halimanes from the Australian rainforest plant Croton Insularis

2019

Journal Article

Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C–H insertion of cubane

Houston, Sevan D., Chalmers, Benjamin A., Savage, G. Paul and Williams, Craig M. (2019). Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C–H insertion of cubane. Organic & Biomolecular Chemistry, 17 (5), 1067-1070. doi: 10.1039/c8ob02959h

Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C–H insertion of cubane

2019

Journal Article

Synthesis of the seco-limonoid BCD ring system identifies a Hsp90 chaperon machinery (p23) inhibitor

Pinkerton, David M., Chow, Sharon, Eisa, Nada H., Kainth, Kashish, Vanden Berg, Timothy J., Burns, Jed M., Guddat, Luke W., Savage, G. Paul, Chadli, Ahmed and Williams, Craig M. (2019). Synthesis of the seco-limonoid BCD ring system identifies a Hsp90 chaperon machinery (p23) inhibitor. Chemistry - A European Journal, 25 (6), 1451-1455. doi: 10.1002/chem.201805420

Synthesis of the seco-limonoid BCD ring system identifies a Hsp90 chaperon machinery (p23) inhibitor

2019

Journal Article

New casbanes and the first trans‐cyclopropane seco‐casbane from the Australian rainforest plant croton insularis

Maslovskaya, Lidiya A., Savchenko, Andrei I., Pierce, Carly J., Boyle, Glen M., Gordon, Victoria A., Reddell, Paul W., Parsons, Peter G. and Williams, Craig M. (2019). New casbanes and the first trans‐cyclopropane seco‐casbane from the Australian rainforest plant croton insularis. Chemistry - A European Journal, 25 (6), 1525-1534. doi: 10.1002/chem.201804904

New casbanes and the first trans‐cyclopropane seco‐casbane from the Australian rainforest plant croton insularis

2019

Journal Article

Hydrogen-bonding interactions in the Ley-Griffith oxidation: practical considerations for the synthetic chemist

Moore, Peter W., Zerk, Timothy J., Burns, Jed M., Bernhardt, Paul V. and Williams, Craig M. (2019). Hydrogen-bonding interactions in the Ley-Griffith oxidation: practical considerations for the synthetic chemist. European Journal of Organic Chemistry, 2019 (2-3), 303-308. doi: 10.1002/ejoc.201800860

Hydrogen-bonding interactions in the Ley-Griffith oxidation: practical considerations for the synthetic chemist

2019

Journal Article

A protocol for an iodine-metal exchange reaction on cubane using lithium organozincates

Kato, Yumi, Williams, Craig M., Uchiyama, Masanobu and Matsubara, Seijiro (2019). A protocol for an iodine-metal exchange reaction on cubane using lithium organozincates. Organic Letters, 21 (2), 473-475. doi: 10.1021/acs.orglett.8b03721

A protocol for an iodine-metal exchange reaction on cubane using lithium organozincates

2019

Conference Publication

Chemistry, mode of action and clinical efficacy of the anticancer diterpenoid tigilanol tigliate (EBC-46)

Appendino, G., Pagani, A., Williams, C., Cullen, J., Boyle, G., Parsons, P., Campbell, J., Gordon,, Schmidt, P. and Reddell, P. (2019). Chemistry, mode of action and clinical efficacy of the anticancer diterpenoid tigilanol tigliate (EBC-46). 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA), Innsbruck, Austria, 1-5 September, 2019. Stuttgart, Germany: Georg Thieme Verlag. doi: 10.1055/s-0039-3399676

Chemistry, mode of action and clinical efficacy of the anticancer diterpenoid tigilanol tigliate (EBC-46)

2019

Journal Article

Correction: The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research

McAlpine, James B., Chen, Shao-Nong, Kutateladze, Andrei, MacMillan, John B., Appendino, Giovanni, Barison, Andersson, Beniddir, Mehdi A., Biavatti, Maique W., Bluml, Stefan, Boufridi, Asmaa, Butler, Mark S., Capon, Robert J., Choi, Young H., Coppage, David, Crews, Phillip, Crimmins, Michael T., Csete, Marie, Dewapriya, Pradeep, Egan, Joseph M., Garson, Mary J., Genta-Jouve, Grégory, Gerwick, William H., Gross, Harald, Harper, Mary Kay, Hermanto, Precilia, Hook, James M., Hunter, Luke, Jeannerat, Damien, Ji, Nai-Yun ... Pauli, Guido F. (2019). Correction: The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research. Natural Product Reports, 36 (1), 248-249. doi: 10.1039/c8np90041h

Correction: The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research

2018

Journal Article

Cover Feature: Hydrogen-Bonding Interactions in the Ley-Griffith Oxidation: Practical Considerations for the Synthetic Chemist (Eur. J. Org. Chem. 2-3/2019)

Moore, Peter W., Zerk, Timothy J., Burns, Jed M., Bernhardt, Paul V. and Williams, Craig M. (2018). Cover Feature: Hydrogen-Bonding Interactions in the Ley-Griffith Oxidation: Practical Considerations for the Synthetic Chemist (Eur. J. Org. Chem. 2-3/2019). European Journal of Organic Chemistry, 2019 (2-3), 230-230. doi: 10.1002/ejoc.201801822

Cover Feature: Hydrogen-Bonding Interactions in the Ley-Griffith Oxidation: Practical Considerations for the Synthetic Chemist (Eur. J. Org. Chem. 2-3/2019)

2018

Journal Article

Commercial AHAS-inhibiting herbicides are promising drug leads for the treatment of human fungal pathogenic infections

Garcia, Mario D., Chua, Sheena M. H., Low, Yu-Shang, Lee, Yu-Ting, Agnew-Francis, Kylie, Wang, Jian-Guo, Nouwens, Amanda, Lonhienne, Thierry, Williams, Craig M., Fraser, James A. and Guddat, Luke W. (2018). Commercial AHAS-inhibiting herbicides are promising drug leads for the treatment of human fungal pathogenic infections. Proceedings of the National Academy of Sciences of the United States of America, 115 (41), E9649-E9658. doi: 10.1073/pnas.1809422115

Commercial AHAS-inhibiting herbicides are promising drug leads for the treatment of human fungal pathogenic infections

2018

Journal Article

The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research

McAlpine, James B., Chen, Shao-Nong, Kutateladze, Andrei, MacMillan, John B., Appendino, Giovanni, Barison, Andersson, Beniddir, Mehdi A., Biavatti, Maique W., Bluml, Stefan, Boufridi, Asmaa, Butler, Mark S., Capon, Robert J., Choi, Young H., Coppage, David, Crews, Phillip, Crimmins, Michael T., Csete, Marie, Dewapriya, Pradeep, Egan, Joseph M., Garson, Mary J., Genta-Jouve, Grégory, Gerwick, William H., Gross, Harald, Harper, Mary Kay, Hermanto, Precilia, Hook, James M., Hunter, Luke, Jeannerat, Damien, Ji, Nai-Yun ... Pauli, Guido F. (2018). The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research. Natural Product Reports, 36 (1), 35-107. doi: 10.1039/c7np00064b

The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research

2018

Journal Article

Corrigendum to: Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere (Angewandte Chemie International Edition, (2016), 55, 11, (3580-3585), 10.1002/anie.201510675)

Chalmers, Benjamin A., Xing, Hui, Houston, Sevan, Clark, Charlotte, Ghassabian, Sussan, Kuo, Andy, Cao, Benjamin, Reitsma, Andrea, Murray, Cody-Ellen P., Stok, Jeanette E., Boyle, Glen M., Pierce, Carly J., Littler, Stuart W., Winkler, David A., Bernhardt, Paul V., Pasay, Cielo, De Voss, James J., McCarthy, James, Parsons, Peter G., Walter, Gimme H., Smith, Maree T., Cooper, Helen M., Nilsson, Susan K., Tsanaktsidis, John, Savage, G. Paul and Williams, Craig M. (2018). Corrigendum to: Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere (Angewandte Chemie International Edition, (2016), 55, 11, (3580-3585), 10.1002/anie.201510675). Angewandte Chemie - International Edition, 57 (28), 8359-8359. doi: 10.1002/anie.201711161

Corrigendum to: Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere (Angewandte Chemie International Edition, (2016), 55, 11, (3580-3585), 10.1002/anie.201510675)