Research record

Publications

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201 publications found

Journal article

Benzo[1,2,3]dithiazole Compounds: A History of Synthesis and Their Renewed Applicability in Materials and Synthetic Chemistry, Originating from the Herz Reaction

A. J. Nicholls; I. R. Baxendale

Reactions · 2021 · 2 · 175–208

The benzo[1,2,3]dithiazole is a unique heteroaromatic functionality whose conjugated profile instils some fascinating electronic properties. This has been historically recognized in the design and manufacture of organic dyes early last century. Although, with…

Journal article

Protein domain-based prediction of drug/ compound-target interactions and experimental validation on LIM kinases

Doğan, T.; Akhan, Güzelcan E.; Baumann, M.; Koyas, A.; Atas, H.; Baxendale, I. R; Martin, M.; Cetin-Atalay, R.

PLoS Comput. Biol. · 2021 · 17(11) · e1009171-1–34

Predictive approaches such as virtual screening have been used in drug discovery with the objective of reducing developmental time and costs. Current machine learning and networkbased approaches have issues related to generalization, usability, or model int…

Journal article

Synthesis of 7-Chloroquinoline Derivatives Using Mixed Lithium-Magnesium Reagents

Murie, V. E.; Nicolino, P. V.; dos Santos, T.; Gambacorta, G.; R. H. V. Nishimura, R. H. V., Perovani, I. S.; Furtado, L. C.; Costa-Lotufo, L. V.; de Oliveira, A. M.; Vessecchi, R.; Baxendale, I. R.; Clososki, G. C.

J. Org. Chem. · 2021 · 86 · 13402–13419

We have prepared a library of functionalized quinolines through the magnesiation of 7-chloroquinolines under mild conditions, employing both batch and continuous flow conditions. The preparation involved the generation of mixed lithium-magnesium intermediat…

Journal article

A One-Pot Divergent Sequence to Pyrazole and Quinoline Derivatives

Gambacorta, G.; Apperley, D. C.; Baxendale, I. R.

Molecules · 2020 · 25 · 2160–2160(14)

The hydroxy-pyrazole and 3-hydroxy oxindole motifs have been utilised in several pharma and agrochemical leads but are distinctly underrepresented in the scientific literature due to the limited routes of preparation. We have developed a one-pot procedure fo…

Book chapter

Ionic Polymerisation and New Approaches to Polymerisation under Flow Conditions

Brocken, L.; Baxendale. I. R.

Flow Chemistry: Integrated Approaches for Practical Applications - Green Chemistry Series · 2020 · Chapter 8 · 257–315

Although ionic polymerisations are a valuable methodology historically they are less widely used because they are considered capricious, requiring significantly more optimisation due to their sensitivity to the specific reaction and processing conditions. …

Journal article

Photochemical Flow Oximation of Alkanes

Griffiths,O. M.; Ruggeri, M.; Baxendale, I. R.

Synlett · 2020 · 19 · 1907–1912

The nitrosation of several alkanes using tert-butyl nitrite has been performed in flow showing a remarkable reduction in the reaction time compared with batch processing. Due to the necessity for large excesses of the alkane component a continuous recyclin…

Book chapter

Radical Polymerisation under Flow Conditions

Brocken, L.; Baxendale. I. R.

Flow Chemistry: Integrated Approaches for Practical Applications · 2020 · Chapter 7 · 217–256

Polymers are an important class of compounds used in many commercial products; for example, in the aerospace and automotive industries functioning as low weight construction parts and seals, through into the packaging of food and drink and even as aqueous s…

Journal article

Rearrangement of 3-Hydroxyazetidines into 2-Oxazolines

Ruggeri, M.; Dombrowski, A. W.; Djuric, S. W.; Baxendale, I. R.

J. Org. Chem. · 2020 · 85 · 7276–7286

A novel rearrangement sequence of 3-hydroxyazetidines via a Ritter initiated cascade provides highly substituted 2-oxazolines in high yields. The reaction conditions and substrate scope of the transformation have been studied demonstrating the generality of t…

Journal article

Straight forward and versatile differentiation of the L-glycero and D-glycero-D-manno heptose scaffold

Suster, C.; Baxendale, I. R.; Mihovilovic, M. D.; Stanetty, C.

Front. Chem. · 2020 · 8 · 1–7

Bacterial lipopolysaccharides (LPS) are important bio-medical structures, playing a major role in the interaction with human immune systems. Their core regions, containing multiple units of L-glycero-D-manno heptoses (L,D-heptose), are highly conserved struct…

Journal article

A Simple and Efficient Flow Preparation of Pyocyanin a Virulence Factor of Pseudomonas aeruginosa

Mortzfeld, F. B.; Pietruszka, J.; Baxendale, I. R.

Euro. J. Org. Chem. · 2019 · X · 5424–5433

The synthesis of the naturally occurring toxin pyocyanin has been realized in a short 4 step sequence. The key photochemical reaction and isolation of the final product have been facilitated by the use of flow chemistry techniques and immobilised reagents. Us…

Journal article

A solid-supported arylboronic acid catalyst for direct amidation

Du, Y.; Barber, T.; Lim, S. E.; Baxendale, I. R.; Whiting, A.

Chem. Commun. · 2019 · 55 · 2916–2919

A new catalyst has been prepared by co-polymerisation of styrene, DVB with 4-styreneboronic acid to derive a efficient heterogeneous direct amidation catalyst. The catalyst shows wide substrate applicability and higher levels of reactivity than the equivalent…

Journal article

Copper-Mediated Nitrosation: 2-Nitrosophenolato Complexes and Their Use in the Synthesis of Heterocycles

Nicholls, A. J.; Batsanov, A. S.; Baxendale, I. R.

Molecules · 2019 · 24(22) · 4154–(1-19)

A simple protocol yielding ortho-substituted nitrosophenols from phenols is demonstrated, in the form of copper(II) bis(nitrosophenolato) complexes. The developed methodology was applied to a range of substrates, confirming the role of the copper in both the …