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One-Pot Sulfoxide Synthesis Exploiting a Sulfinyl-Dication Equivalent Generated from a DABSO/Trimethylsilyl Chloride Sequence

Organic letters, 2016-05, Vol.18 (9), p.2086-2089

2016

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Sustainable organophosphorus-catalysed Staudinger reduction

Green chemistry : an international journal and green chemistry resource : GC, 2018, Vol.20 (19), p.4418-4422

2018

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Catalytic Staudinger Reduction at Room Temperature

Journal of organic chemistry, 2019-05, Vol.84 (10), p.6536-6545

2019

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Triphenylphosphine-catalysed amide bond formation between carboxylic acids and amines

Chemical communications (Cambridge, England), 2014-06, Vol.50 (43), p.5763-5766

2014

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Zirconium-catalyzed direct amide bond formation between carboxylic esters and amines

Tetrahedron, 2015-08, Vol.71 (34), p.5547-5553

2015

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Inhibition of histone lysine methyltransferases G9a and GLP by ejection of structural Zn(II)

Bioorganic & medicinal chemistry letters, 2018-04, Vol.28 (7), p.1234-1238

2018

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Chemoselective calcium-catalysed direct amidation of carboxylic esters

RSC advances, 2015-01, Vol.5 (95), p.77658-77661

2015

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Poly(methylhydrosiloxane) as a green reducing agent in organophosphorus-catalysed amide bond formation

Organic & biomolecular chemistry, 2017-08, Vol.15 (30), p.6426-6432

2017

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(R)‐PFI‐2 Analogues as Substrates and Inhibitors of Histone Lysine Methyltransferase SETD7

ChemMedChem, 2023-12, Vol.18 (23), p.e202300457-n/a

2023

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Importance of the main chain of lysine for histone lysine methyltransferase catalysis

Organic & biomolecular chemistry, 2019-06, Vol.17 (23), p.5693-5697

2019

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Lysine Ethylation by Histone Lysine Methyltransferases

Chembiochem : a European journal of chemical biology, 2020-02, Vol.21 (3), p.392-400

2020

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Investigating the active site of human trimethyllysine hydroxylase

Biochemical journal, 2019-04, Vol.476 (7), p.1109-1119

2019

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Examining sterically demanding lysine analogs for histone lysine methyltransferase catalysis

Scientific reports, 2020-02, Vol.10 (1), p.3671-3671, Article 3671

2020

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Novel SAR for quinazoline inhibitors of EHMT1 and EHMT2

Bioorganic & medicinal chemistry letters, 2019-09, Vol.29 (17), p.2516-2524

2019

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Sustainable organophosphorus-catalysed Staudinger reductionElectronic supplementary information (ESI) available: Synthetic procedures, characterisation of compounds, and NMR spectra. See DOI: 10.1039/c8gc02136h

2018-10

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Front Cover

ChemMedChem, 2023-12, Vol.18 (23)

2023

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Front Cover: (R)‐PFI‐2 Analogues as Substrates and Inhibitors of Histone Lysine Methyltransferase SETD7 (ChemMedChem 23/2023)

ChemMedChem, 2023-12, Vol.18 (23), p.n/a

2023

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Triphenylphosphine-catalysed amide bond formation between carboxylic acids and aminesElectronic supplementary information (ESI) available: Synthetic procedures, characterisation of compounds, and chiral HPLC data. See DOI: 10.1039/c4cc01861c

2014-05

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Poly(methylhydrosiloxane) as a green reducing agent in organophosphorus-catalysed amide bond formationElectronic supplementary information (ESI) available: Synthetic procedures, characterisation of compounds, and NMR spectra. See DOI: 10.1039/c7ob01510k

2017-08

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ChemInform Abstract: Chemoselective Calcium‐Catalyzed Direct Amidation of Carboxylic Esters

ChemInform, 2016-01, Vol.47 (6), p.no-no

2016

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ChemInform Abstract: Zirconium-Catalyzed Direct Amide Bond Formation Between Carboxylic Esters and Amines

ChemInform, 2015-12, Vol.46 (50), p.no-no

2015

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ChemInform Abstract: One‐Pot Sulfoxide Synthesis Exploiting a Sulfinyl‐Dication Equivalent Generated from a DABSO/Trimethylsilyl Chloride Sequence

ChemInform, 2016-08, Vol.47 (37), p.no-no

2016

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Chemoselective calcium-catalysed direct amidation of carboxylic estersElectronic supplementary information (ESI) available: Reaction optimisation, background reactions, characterisation of products. See DOI: 10.1039/c5ra18288c

2015-09

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Organic Synthesis in Flow: Toward Higher Levels of Sustainability

Sustainable Flow Chemistry, 2017, p.103-134

2017

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ChemInform Abstract: Triphenylphosphine-Catalyzed Amide Bond Formation Between Carboxylic Acids and Amines

ChemInform, 2014-09, Vol.45 (38), p.no-no

2014

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One-Pot Sulfoxide Synthesis Exploiting a Sulfinyl-Dication Equivalent Generated from a DABSO/Trimethylsilyl Chloride Sequence

Sustainable organophosphorus-catalysed Staudinger reduction

Catalytic Staudinger Reduction at Room Temperature

Triphenylphosphine-catalysed amide bond formation between carboxylic acids and amines

Zirconium-catalyzed direct amide bond formation between carboxylic esters and amines

Inhibition of histone lysine methyltransferases G9a and GLP by ejection of structural Zn(II)

Chemoselective calcium-catalysed direct amidation of carboxylic esters

Poly(methylhydrosiloxane) as a green reducing agent in organophosphorus-catalysed amide bond formation

(R)‐PFI‐2 Analogues as Substrates and Inhibitors of Histone Lysine Methyltransferase SETD7

Importance of the main chain of lysine for histone lysine methyltransferase catalysis

Lysine Ethylation by Histone Lysine Methyltransferases

Investigating the active site of human trimethyllysine hydroxylase

Examining sterically demanding lysine analogs for histone lysine methyltransferase catalysis

Novel SAR for quinazoline inhibitors of EHMT1 and EHMT2

Sustainable organophosphorus-catalysed Staudinger reductionElectronic supplementary information (ESI) available: Synthetic procedures, characterisation of compounds, and NMR spectra. See DOI: 10.1039/c8gc02136h

Front Cover

Front Cover: (R)‐PFI‐2 Analogues as Substrates and Inhibitors of Histone Lysine Methyltransferase SETD7 (ChemMedChem 23/2023)

Triphenylphosphine-catalysed amide bond formation between carboxylic acids and aminesElectronic supplementary information (ESI) available: Synthetic procedures, characterisation of compounds, and chiral HPLC data. See DOI: 10.1039/c4cc01861c

Poly(methylhydrosiloxane) as a green reducing agent in organophosphorus-catalysed amide bond formationElectronic supplementary information (ESI) available: Synthetic procedures, characterisation of compounds, and NMR spectra. See DOI: 10.1039/c7ob01510k

ChemInform Abstract: Chemoselective Calcium‐Catalyzed Direct Amidation of Carboxylic Esters

ChemInform Abstract: Zirconium-Catalyzed Direct Amide Bond Formation Between Carboxylic Esters and Amines

ChemInform Abstract: One‐Pot Sulfoxide Synthesis Exploiting a Sulfinyl‐Dication Equivalent Generated from a DABSO/Trimethylsilyl Chloride Sequence

Chemoselective calcium-catalysed direct amidation of carboxylic estersElectronic supplementary information (ESI) available: Reaction optimisation, background reactions, characterisation of products. See DOI: 10.1039/c5ra18288c

Organic Synthesis in Flow: Toward Higher Levels of Sustainability

ChemInform Abstract: Triphenylphosphine-Catalyzed Amide Bond Formation Between Carboxylic Acids and Amines

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