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Australian Journal of Chemistry

Australian Journal of Chemistry

Volume 78 Number 8 2025

CH25070The value of telling it like it was. The best honours project ever?

Christopher Barnett 0000-0002-8818-6908, Thomas Maschmeyer, Anthony F. Masters and Alexander K. L. Yuen 0000-0002-6908-8851

Cartoon by Sidney Harris of a reviewer of a chemical process saying ‘I think you should be more explicit here in step two’ where it says ‘Then a miracle occurs’

Undergraduate students should appreciate that chemical understanding is not static; what we teach is our ‘best guess’ to explain observables. Textbooks frequently conflate (and often incorrectly describe) the concept of the nucleus, inferred by Rutherford from Marsden’s ‘gold foil’ experiment, with the model of the nucleus, containing protons and neutrons, despite nearly 25 years between these advances. We argue that an opportunity is lost in the teaching of chemistry, to illustrate to students the incremental progress in chemistry and that the ‘wrong’ explanation can be very useful. (Image credit: © Sidney Harris, originally appearing in American Scientist in 1977, reproduced with permission.)

CH25086Rational design and selection of next-generation cyclotide drugs using the knotted cyclic peptide scaffold MCoTI-II

Sven Ullrich 0000-0003-4184-7024, Grégoire Jean-Baptiste Philippe 0000-0001-8103-9211, Choi Yi Li 0000-0001-8823-3666 and Hiroaki Suga 0000-0002-5298-9186

Schematic showing the solution structure of MCoTI-II with cystine-knotted disulfide bridges highlighted.

This mini-review highlights tactics to engineer MCoTI-II, a cyclic cystine-knot peptide natural product, into next-generation therapeutics and diagnostics. Through both rational modification and genetically encoded selection platforms, variants of the MCoTI-II cyclotide have been developed for a diverse range of potential biomedical applications. (Image credit: Sven Ullrich.)

This article belongs to the collection: 70th Birthday tribute to Prof. David Craik.


Friedel–Crafts cyclisations of indole carboxylic acids or indole alcohols to tetracyclic azopinoindoles.

Indole fused N-heterocycles form the structural core of a large number of natural products and pharmaceuticals. These properties make them exciting targets for synthetic chemists, with a wide range of synthetic methodologies reported. However, these often have a number of drawbacks, including cost, scalability and low yields. Herein, we explore an efficient construction of benzo-, pyrido-, thieno-, naphtho-fused azepinoindolones and indolo-azepinoquinolinones from readily available starting materials through Lewis and Brønsted acid mediated Friedel–Crafts reactions. (Image credit: Hassan A. K. Abd El-Aal.)

CH25050An unusual triterpene fatty acid conjugate from Dodonaea caespitosa

Andrew M. Bloomfield 0000-0003-4449-6872, Eugene Eades, Hendra Gunosewoyo 0000-0003-3897-1948 and Alan D. Payne 0000-0003-4530-6348

Chemical structure of the betulin conjugate 2 extracted from Dodonaea caespitosa.

The south-west of Western Australia is a biodiversity hotspot, where collaborations between local communities and scientists play a pivotal role in the study of native plants. The leaf resin of Dodonaea caespitosa, growing in Nowanup, contained only two compounds, one of which was an unusual bioconjugate comprising a triterpene, a cutin monomer and a p-hydroxycinnamate. This natural product was the first isolated to date and will help our understanding of the biology and ecology of this plant. (Image credit: Andrew M. Bloomfield.)

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