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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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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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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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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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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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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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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 an international journal of organic chemistry, 2023-07, Vol.10 (14), p.3460-3466

2023

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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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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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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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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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The Bull-James assembly as a chiral auxiliary and shift reagent in kinetic resolution of alkyne amines by the CuAAC reactionDedicated to the 60th Birthday of Tony Czarnik.1Electronic supplementary information (ESI) available. CCDC 1477891. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6ob01623e

2016-11

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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

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

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

Synthesis of complex unnatural fluorine-containing amino acids

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

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

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

Synthesis of pentafluorosulfanyl (SF5) containing aromatic amino acids

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

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

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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