Recent & Highlight Publications
Full listings of the (>200) group publications are available from Web of Knowledge or Google Scholar. Open access requirements are dealt with by the Nottingham eprints facility, which can be accessed from here (link).
Current Highlight Publication for 2025: Homogeneous catalyst graph neural network: A human-interpretable graph neural network tool for ligand optimization in asymmetric catalysis [iScience (Cell Press) doi]
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Already under use in other laboratories.
2024: Probing the Mechanism of Action of Bis-phenolato Amine (ONO donor set) Titanium(IV) Anti-Cancer Agents [J. Med. Chem. doi]
2023: Can "Electric Flare Stacks" Reduce CO2 Emissions? A Case Study with Non Thermal Plasma [Ind. Eng. Chem. Res. doi]
2023: Scalable Synthesis of Chiral Himbert Diene Ligands for Asymmetric Catalysis [Adv. Synth. Catal. doi]
Front cover of edition
2023: Catalysis enabled synthesis, structures, and reactivities of fluorinated S8-corona[n]arenes (n = 8–12) [Chemical Science doi]
One of the Jan 2023 covers
2023: Design, and synthesis of selectively anticancer 4-cyanophenyl substituted thiazol-2-ylhydrazones [RSC Advances doi]
2022: Rate of Formation of Industrial Lubricant Additive Precursors from Maleic Anhydride and Polyisobutylene [OPRD doi]
2022: Machine learnt patterns in rhodium-catalysed asymmetric Michael addition using chiral diene ligands [Results in Chemistry doi]
2022: Identifying Chirality in Line Drawings of Molecules Using Imbalanced Dataset Sampler for a Multilabel Classification Task [Molecular Informatics doi]
Try the tool or add to the data set
2019: Tripodal O-N-O Bis-Phenolato Amine Titanium(IV) Complexes Show High in vitro Anti-Cancer Activity [Eur J Inorg Chem doi]
2017: Kinetic Analysis of Copper(I)/Feringa-Phosphorannidite Catalyzed AIEt3 1,4-Addition to Cyclohex-2-en-1-one [ACS Catalysis doi]
ACS 'paper of the day' 21 Sept
2017: Low-Cost and Sustainable Organic Thermoelectrics Based on Low-Dimensional Molecular Metals [Advanced Materials doi]
2017: Straightforward Synthesis of 2-and 2,8-Substituted Tetracenes [Chem Eur J doi]
