Pilarski Group

Synthetic methodology, catalysis and green chemistry
Organic molecules underpin huge areas of modern life, from pharmaceuticals to functional materials and beyond. However, making the molecules society needs can be enormously challenging, inefficient and expensive. New methods in organic synthesis are needed all the time.
Our group invents and develops new methods to build organic molecules in ever faster, cheaper and more environmentally sustainable ways. We use several strategies to achieve this. These include:
- Catalytic C-H functionalisation
- Aryne Chemistry
- Mechanochemistry
Group members
Publications
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Solventless Catalytic C-H and C-X Functionalization without Ball Milling
Part of Journal of Organic Chemistry, p. 8846-8856, 2025
- DOI for Solventless Catalytic C-H and C-X Functionalization without Ball Milling
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Access to long-lived room temperature phosphorescence through auration of 2,1,3-benzothiadiazole
Part of Dalton Transactions, p. 5658-5664, 2024
- DOI for Access to long-lived room temperature phosphorescence through auration of 2,1,3-benzothiadiazole
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Part of Journal of Organic Chemistry, p. 6138-6148, 2024
- DOI for Derivatization of 2,1,3-Benzothiadiazole via Regioselective C–H Functionalization and Aryne Reactivity
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Synthesis and crystal structures of boryl ortho-silylaryl trifluoromethanesulfonates
Part of Acta Crystallographica Section E, p. 143-147, 2024
- DOI for Synthesis and crystal structures of boryl ortho-silylaryl trifluoromethanesulfonates
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Solvent-free and ball mill-free catalytic C–H methylation
Part of Green Chemistry, p. 9138-9145, 2023
- DOI for Solvent-free and ball mill-free catalytic C–H methylation
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Mechanochemical Solvent-Free Catalytic C-H Methylation
Part of Angewandte Chemie International Edition, p. 6660-6666, 2021
- DOI for Mechanochemical Solvent-Free Catalytic C-H Methylation
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Mechanochemical synthesis of (hetero)aryl Au(i) complexes
Part of Green Chemistry, p. 5648-5655, 2020
- DOI for Mechanochemical synthesis of (hetero)aryl Au(i) complexes
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Mild and Efficient Synthesis of Diverse Organo-Au-I-L Complexes in Green Solvents
Part of ChemSusChem, p. 2032-2037, 2020
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Arynes and Their Precursors from Arylboronic Acids via Catalytic C-H Silylation
Part of Journal of Organic Chemistry, p. 5863-5871, 2019
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Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations
Part of Molecules, 2019
- DOI for Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations
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C4-H indole functionalisation: precedent and prospects
Part of Chemical Science, p. 4203-4216, 2018
- DOI for C4-H indole functionalisation: precedent and prospects
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Young Career Focus: Dr. Lukasz T. Pilarski (Uppsala University, Sweden)
Part of Synlett, 2017
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Ru-Catalysed C-H Silylation of Gramines, Tryptamines and their Congeners
Part of Chemical Communications, p. 5868-5871, 2016
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Part of Synlett, p. 969-976, 2016
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Part of Synlett, p. 969-976, 2016
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Part of Angewandte Chemie International Edition, p. 11765-11769, 2015
- DOI for Boryl (Hetero)aryne Precursors as Versatile Arylation Reagents: Synthesis through C-H Activation and Orthogonal Reactivity
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Ru-Catalysed C-H Arylation of Indoles and Pyrroles with Boronic Acids: Scope and Mechanistic Studies
Part of Chemistry - A European Journal, p. 5380-5386, 2015
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Part of Acta Crystallographica Section E, p. 1190-+, 2015
- DOI for Crystal structure of acetonitrile[eta(6)-1-methyl-4-(1-methylethyl)benzene][1-(pyrimidin-2-yl )-3H-indol-1-ium-2-yl-kappa N-2,C]ruthenium(II) bis-(hexafluoridoantimonate)
- Download full text (pdf) of Crystal structure of acetonitrile[eta(6)-1-methyl-4-(1-methylethyl)benzene][1-(pyrimidin-2-yl )-3H-indol-1-ium-2-yl-kappa N-2,C]ruthenium(II) bis-(hexafluoridoantimonate)
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Synthesis of aryne precursors via transition metal-catalyzed C-H silylation
Part of Abstracts of Papers of the American Chemical Society, 2014
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Part of Abstracts of Papers of the American Chemical Society, 2014
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Benchmarking computational methods for the optimisation of aryne and cycloalkyne geometries
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Elucidating structure-distortion relationships in arynes and cycloalkynes
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Aryne Capture Regiocontrol via Fluoroboronate-induced Distortion
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Chemo- and Regioselective Generation of the 1,3-Benzdiyne Synthon
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