Jackson Henneveld

Mr Jackson Henneveld

Grant-Funded Researcher (A)

SAIGENCI

College of Health


Postdoctoral Researcher, Drug Discovery Chemistry
Adelaide Drug Discovery Incubator (ADDI) + Molecular & Proximity Discovery (MPD) Lab, SAiGENCI

Year Citation
2025 Craig, A. J., Cording, A. P., Gilmer, S. C. L., Henneveld, J. S., Gai, S., Harker, O. H., . . . Hawkins, B. C. (2025). The Synthesis of Cyclopropyl-Fused Tetrahydrofurans from Vinylcyclopropanes. Asian Journal of Organic Chemistry, 14(9), 5 pages.
DOI
2025 Henneveld, J. S., Lucas, N. T., Bissember, A. C., & Hawkins, B. C. (2025). Dipole-Transmissive 1,3-Dipolar Cycloadditions: Modular, Diversity-Oriented Synthesis of Polycyclic Alkaloid Scaffolds. Organic Letters, 27(22), 5917-5923.
DOI Scopus2 WoS2 Europe PMC1
2023 Henneveld, J. S., Shiri, F., Ariafard, A., Lucas, N. T., Bissember, A. C., & Hawkins, B. C. (2023). Dipole‐Transmissive 1,3‐Dipolar Cycloadditions for the Rapid Construction of Polycyclic N‐Heterocycles: Synthetic and Mechanistic Investigations. Chemistry - A European Journal, 29(42), e202301254-1-e202301254-7.
DOI Scopus6 WoS6 Europe PMC5
2022 Olivier, W. J., Henneveld, J. S., Smith, J. A., Hawkins, B. C., & Bissember, A. C. (2022). Strategies for the synthesis of 𝘚𝘵𝘦𝘮𝘰𝘯𝘢 alkaloids:
an update. Natural product reports (Print), 39(12), 2308-2335.

DOI Scopus16 WoS14 Europe PMC7
2021 Gai, S., Henneveld, J. S., Cording, A. P., Badart, M. P., Lucas, N. T., & Hawkins, B. C. (2021). The synthesis of benzannulated spiroketals from 1,1-diacyl-2-phenylcyclopropanes. Tetrahedron Letters, 69, 4 pages.
DOI Scopus5 WoS5
2021 Henneveld, J. S., Gilmer, S. C. L., Lucas, N. T., & Hawkins, B. C. (2021). Rapid Generation of 2-Acyl-4-phenyltetralones from 1,1-Diacylphenylcyclopropanes. Asian Journal of Organic Chemistry, 10(10), 2553-2556.
DOI Scopus3 WoS3

Year Citation
2021 Bissember, A. C., Hyland, C. J. T., Wales, S. M., Hawkins, B. C., Chen, J. L. Y., Fleming, C. L., . . . Zarfos, S. D. (2021). Seven-membered rings. In Progress in Heterocyclic Chemistry (Vol. 33, pp. 533-581). Elsevier.
DOI Scopus3

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