We are delighted to present the 2024 edition of the RSC Advances Emerging Investigators series! Following the success of our 2023 edition, we are excited to continue highlighting the chemistry research being conducted by some of the leading investigators in our community.
This year’s Series Editors were Professor Shirley Nakagaki (Federal University of Paraná, Brazil) and Professor Fabienne Dumoulin (Acıbadem Mehmet Ali Aydınlar Universit, Türkiye). Nine articles were selected to support emerging researchers who are already making strides in their respective fields of research, both nationally and internationally. This series focused on interesting studies showcasing researchers’ efforts to obtain information that could potentially address the United Nations Sustainable Development Goals (UN SDGs). Here we showcase publications that present an advance in chemistry and support societal efforts for sustainable development. Read all about the collection in this accompanying Editorial.
We would like to take this opportunity to highlight an author from the series, Valerio Fasano . We interviewed Valerio about his work.
Valerio Fasano

First total synthesis of caerulomycin K: a case study on selective, multiple C–H functionalizations of pyridines
Alessandro Dimasi, Mattia Failla, Arianna Montoli, Andrea Citarella, Paolo Ronchi, Daniele Passarella and Valerio Fasano
RSC Adv., 2024,14, 5542-5546
Dr Valerio Fasano earned his B.Sc. from the University of Catania and M.Sc. from the University of Bologna (Italy). After a research visit to the University of Lund (Sweden), he completed his Ph.D. at the University of Manchester (UK) under Prof. Michael Ingleson. Supported by a Royal Society of Chemistry mobility grant, he joined Prof. Douglas Stephan at the University of Toronto (Canada). He then returned to the UK as a Doctoral Prize Fellow at the University of Bristol with Prof. Varinder Aggarwal. In 2023, he became a Tenure Track Assistant Professor at the University of Milan (Italy), where he was promoted to Associate Professor in 2026.
Could you briefly explain the focus of your article to the non-specialist and why it is of current interest?
We achieved the first total synthesis of caerulomycin K, a natural product isolated from marine-derived bacteria. This pyridine-based alkaloid is of interest due to its antimicrobial potential and relevance in natural product chemistry.
How big an impact could your results potentially have?
Although structurally simple, previous syntheses of similar molecules required numerous steps. Our new three-step route offers a rapid and efficient access to caerulomycin K, enabling the swift preparation of related analogues for biological evaluation.
Could you explain the motivation behind this study?
Our group focuses on the total synthesis of natural products and the functionalization of nitrogen-containing heterocycles. Caerulomycin K was an ideal target as it lies at the intersection of both research areas.
In your opinion, what are the key design considerations for your study?
From the outset, we aimed to synthesize caerulomycin K without relying on pre-functionalized intermediates, instead using selective C–H functionalization of N-heterocycles. Achieving this required testing several strategies before identifying the successful one.
Which part of the work towards this paper proved to be most challenging?
Our initial approach relied on a double functionalization of the pyridine ring, which could have allowed tunable derivatization. Despite promising attempts, this strategy ultimately proved unfeasible.
What aspect of your work are you most excited about at the moment?
Achieving a concise, three-step total synthesis of caerulomycin K is particularly exciting, as it opens the door to rapidly generating diverse analogues for further study.
How has your research evolved from your first article to this particular article?
While we continue to explore N-heterocycle functionalization, our research has expanded to include isotopic labelling and the study of boron-containing heterocycles.
What is the next step? What work is planned?
We are developing new methodologies for heterocycle functionalization, with a particular focus on integrating photocatalysis and automated synthesis technologies.
Why did you want to publish in RSC Advances?
The Royal Society of Chemistry is a long-standing and highly respected institution. RSC Advances offers excellent visibility and scientific credibility, making it an ideal platform for our work.
What are your thoughts on open access publishing?
I strongly support open access, as science should be freely accessible to all. My main concern, however, is the rise of predatory journals, which threaten the quality and integrity of scientific research.

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