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Carboxylic Acid Deoxyfluorination and One-Pot Amide Bond Formation Using Pentafluoropyridine (PFP)

Organic letters, 2021-08, Vol.23 (15), p.5793-5798

2021

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Negishi cross-couplings in the synthesis of amino acids

Organic & biomolecular chemistry, 2018-01, Vol.16 (1), p.1-2

2018

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Aminoacyl chain translocation catalysed by a type II thioesterase domain in an unusual non-ribosomal peptide synthetase

Nature communications, 2022-01, Vol.13 (1), p.62-62, Article 62

2022

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One-pot ester and thioester formation mediated by pentafluoropyridine (PFP)

Organic & biomolecular chemistry, 2022-10, Vol.2 (41), p.859-864

2022

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Rapid Determination of Enantiomeric Excess via NMR Spectroscopy: A Research-Informed Experiment

Journal of chemical education, 2017-01, Vol.94 (1), p.79-84

2017

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Synthesis of complex unnatural fluorine-containing amino acids

Journal of fluorine chemistry, 2020-11, Vol.239, p.109630-109630, Article 109630

2020

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Recent advances in the use of chiral metal complexes with achiral ligands for application in asymmetric catalysis

Catalysis science & technology, 2015-01, Vol.5 (7), p.3441-3451

2015

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Kinetic resolution of alkyne-substituted quaternary oxindoles via copper catalysed azide-alkyne cycloadditions

Chemical communications (Cambridge, England), 2015-12, Vol.51 (97), p.17217-17220

2015

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N-Terminal speciation for native chemical ligation

Chemical communications (Cambridge, England), 2020-06, Vol.56 (45), p.6114-6117

2020

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Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation

Scientific reports, 2019-10, Vol.9 (1), p.15086-9, Article 15086

2019

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Synthesis of atropisomeric phosphino-triazoles and their corresponding gold( i ) complexes

Organic Chemistry Frontiers, 2023-07, Vol.10 (14), p.3460-3466

2023

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Perfluoroaryl and Perfluoroheteroaryl Reagents as Emerging New Tools for Peptide Synthesis, Modification and Bioconjugation

Chemistry : a European journal, 2022-02, Vol.28 (7), p.e202103305-n/a

2022

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Synthesis of pentafluorosulfanyl (SF5) containing aromatic amino acids

Journal of fluorine chemistry, 2018-08, Vol.212, p.166-170

2018

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The Bull-James assembly as a chiral auxiliary and shift reagent in kinetic resolution of alkyne amines by the CuAAC reaction

Organic & biomolecular chemistry, 2016-11, Vol.14 (46), p.10778-10782

2016

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Synthesis of metal-binding amino acids

Organic & biomolecular chemistry, 2024-10

2024

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Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions

Organic & biomolecular chemistry, 2019-02, Vol.17 (8), p.2110-2115

2019

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Asymmetric Copper-Catalyzed Azide–Alkyne Cycloadditions

ACS catalysis, 2016-06, Vol.6 (6), p.3629-3636

2016

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Protecting Group-Controlled Remote Regioselective Electrophilic Aromatic Halogenation Reactions

Journal of organic chemistry, 2020-06, Vol.85 (11), p.6862-6871

2020

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Frontispiece: Perfluoroaryl and Perfluoroheteroaryl Reagents as Emerging New Tools for Peptide Synthesis, Modification and Bioconjugation

Chemistry : a European journal, 2022-02, Vol.28 (7), p.n/a

2022

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HFO‐1234yf as a CF3 Building Block: Synthesis of Trifluoromethyl Quinoline and Chromene Derivatives from Trifluoromethyl‐ynones

European journal of organic chemistry, 2023-03, Vol.26 (11), p.n/a

2023

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Predicting the increase in electron affinity of phenoxy upon fluorination

Journal of fluorine chemistry, 2024-07, Vol.277, p.110306, Article 110306

2024

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Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditionsElectronic supplementary information (ESI) available. CCDC 1856218-1856219. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ob02899k

2019-02

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Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions† †Electronic supplementary information (ESI) available. CCDC 1856218–1856219. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ob02899k

Organic & biomolecular chemistry, 2019-01, Vol.17 (8), p.2110-2115

2019

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HFO‐1234yf as a CF 3 Building Block: Synthesis of Trifluoromethyl Quinoline and Chromene Derivatives from Trifluoromethyl‐ynones

European journal of organic chemistry, 2023-03, Vol.26 (11)

2023

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Kinetic resolution of alkyne-substituted quaternary oxindoles via copper catalysed azide-alkyne cycloadditionsElectronic supplementary information (ESI) available: Experimental procedures, HPLC traces, NMR data and detailed screening tables. See DOI: 10.1039/c5cc04886a

2015-11

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Carboxylic Acid Deoxyfluorination and One-Pot Amide Bond Formation Using Pentafluoropyridine (PFP)

Negishi cross-couplings in the synthesis of amino acids

Aminoacyl chain translocation catalysed by a type II thioesterase domain in an unusual non-ribosomal peptide synthetase

One-pot ester and thioester formation mediated by pentafluoropyridine (PFP)

Rapid Determination of Enantiomeric Excess via NMR Spectroscopy: A Research-Informed Experiment

Synthesis of complex unnatural fluorine-containing amino acids

Recent advances in the use of chiral metal complexes with achiral ligands for application in asymmetric catalysis

Kinetic resolution of alkyne-substituted quaternary oxindoles via copper catalysed azide-alkyne cycloadditions

N-Terminal speciation for native chemical ligation

Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation

Synthesis of atropisomeric phosphino-triazoles and their corresponding gold( i ) complexes

Perfluoroaryl and Perfluoroheteroaryl Reagents as Emerging New Tools for Peptide Synthesis, Modification and Bioconjugation

Synthesis of pentafluorosulfanyl (SF5) containing aromatic amino acids

The Bull-James assembly as a chiral auxiliary and shift reagent in kinetic resolution of alkyne amines by the CuAAC reaction

Synthesis of metal-binding amino acids

Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions

Asymmetric Copper-Catalyzed Azide–Alkyne Cycloadditions

Protecting Group-Controlled Remote Regioselective Electrophilic Aromatic Halogenation Reactions

Frontispiece: Perfluoroaryl and Perfluoroheteroaryl Reagents as Emerging New Tools for Peptide Synthesis, Modification and Bioconjugation

HFO‐1234yf as a CF3 Building Block: Synthesis of Trifluoromethyl Quinoline and Chromene Derivatives from Trifluoromethyl‐ynones

Predicting the increase in electron affinity of phenoxy upon fluorination

Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditionsElectronic supplementary information (ESI) available. CCDC 1856218-1856219. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ob02899k

Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions† †Electronic supplementary information (ESI) available. CCDC 1856218–1856219. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ob02899k

HFO‐1234yf as a CF 3 Building Block: Synthesis of Trifluoromethyl Quinoline and Chromene Derivatives from Trifluoromethyl‐ynones

Kinetic resolution of alkyne-substituted quaternary oxindoles via copper catalysed azide-alkyne cycloadditionsElectronic supplementary information (ESI) available: Experimental procedures, HPLC traces, NMR data and detailed screening tables. See DOI: 10.1039/c5cc04886a

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