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Synthesis of [18F]Arenes via the Copper-Mediated [18F]Fluorination of Boronic Acids

Organic letters, 2015-12, Vol.17 (23), p.5780-5783

2015

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Copper-Catalyzed [18F]Fluorination of (Mesityl)(aryl)iodonium Salts

Organic letters, 2014-06, Vol.16 (12), p.3224-3227

2014

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Late-stage [ 18 F]fluorination: new solutions to old problems

Chemical science (Cambridge), 2014-01, Vol.5 (12), p.4545-4553

2014

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Protecting group free radical C-H trifluoromethylation of peptides

Chemical science (Cambridge), 2018, Vol.9 (17), p.4168-4175

2018

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Synthesis of high-molar-activity [ 18 F]6-fluoro-L-DOPA suitable for human use via Cu-mediated fluorination of a BPin precursor

Nature protocols, 2020-05, Vol.15 (5), p.1742-1759

2020

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Development of Customized [ 18 F]Fluoride Elution Techniques for the Enhancement of Copper-Mediated Late-Stage Radiofluorination

Scientific reports, 2017-03, Vol.7 (1), p.233-233, Article 233

2017

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One-pot synthesis of high molar activity 6-[ 18 F]fluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor

Organic & biomolecular chemistry, 2019, Vol.17 (38), p.8701-8705

2019

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Mechanistic Investigations of Cu-Catalyzed Fluorination of Diaryliodonium Salts: Elaborating the CuI/CuIII Manifold in Copper Catalysis

Organometallics, 2014-10, Vol.33 (19), p.5525-5534

2014

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Automated synthesis of PET radiotracers by copper‐mediated 18F‐fluorination of organoborons: Importance of the order of addition and competing protodeborylation

Journal of labelled compounds & radiopharmaceuticals, 2018-03, Vol.61 (3), p.228-236

2018

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Pd-Catalyzed Decarbonylative Cross-Couplings of Aroyl Chlorides

Organic letters, 2017-08, Vol.19 (15), p.4142-4145

2017

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Palladium- and Nickel-Catalyzed Decarbonylative C–S Coupling to Convert Thioesters to Thioethers

Organic letters, 2018-01, Vol.20 (1), p.44-47

2018

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Cu-Catalyzed Fluorination of Diaryliodonium Salts with KF

Organic letters, 2013-10, Vol.15 (19), p.5134-5137

2013

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Mechanistic Investigations of Cu-Catalyzed Fluorination of Diaryliodonium Salts: Elaborating the Cu I /Cu III Manifold in Copper Catalysis

Organometallics, 2014-10, Vol.33 (19), p.5525-5534

2014

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Catalytic Sulfamoylation of Alcohols with Activated Aryl Sulfamates

Organic letters, 2020-01, Vol.22 (1), p.168-174

2020

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C-H 18F-fluorination of 8-methylquinolines with Ag[18F]FElectronic supplementary information (ESI) available: Experimental procedures, optimization details, radio-HPLC/TLC traces and spectral data. See DOI: 10.1039/c9cc00641a

2019-03

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Synthesis of High Molar Activity [18F]6-Fluoro-L-DOPA Suitable for Human Use by Cu-Mediated Fluorination of a BPin Precursor

Nature protocols, 2020-04, Vol.15 (5), p.1742-1759

2020

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C-H 18 F-fluorination of 8-methylquinolines with Ag[ 18 F]F

Chemical communications (Cambridge, England), 2019-03, Vol.55 (20), p.2976-2979

2019

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C–H 18F-fluorination of 8-methylquinolines with Ag[18F]F

Chemical communications (Cambridge, England), 2019-03, Vol.55 (20), p.2976-2979

2019

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Synthesis of [18F]-γ-Fluoro-α,β-unsaturated Esters and Ketones via Vinylogous 18F-Fluorination of α-Diazoacetates with [18F]AgF

Synthesis (Stuttgart), 2019-12, Vol.51 (23), p.4401-4407

2019

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One-pot synthesis of high molar activity 6-18Ffluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor

Organic & biomolecular chemistry, 2019-10, Vol.17 (38), p.8701

2019

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One-pot synthesis of high molar activity 6-[F]fluoro--DOPA by Cu-mediated fluorination of a BPin precursor

Organic & biomolecular chemistry, 2019-10, Vol.17 (38), p.871-875

2019

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Reducing Limitation in Probe Design: The Development of a Diazirine-Compatible Suzuki–Miyaura Cross Coupling Reaction

ACS medicinal chemistry letters, 2019-01, Vol.10 (1), p.56-61

2019

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One-pot synthesis of high molar activity 6-[18F]fluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor

Organic & biomolecular chemistry, 2019-09, Vol.17 (38)

2019

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Protecting group free radical C-H trifluoromethylation of peptidesElectronic supplementary information (ESI) available. See DOI: 10.1039/c8sc00368h

2018-05

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Protecting group free radical C–H trifluoromethylation of peptides† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc00368h

Chemical science (Cambridge), 2018-04, Vol.9 (17), p.4168-4175

2018

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Synthesis of [18F]Arenes via the Copper-Mediated [18F]Fluorination of Boronic Acids

Copper-Catalyzed [18F]Fluorination of (Mesityl)(aryl)iodonium Salts

Late-stage [ 18 F]fluorination: new solutions to old problems

Protecting group free radical C-H trifluoromethylation of peptides

Synthesis of high-molar-activity [ 18 F]6-fluoro-L-DOPA suitable for human use via Cu-mediated fluorination of a BPin precursor

Development of Customized [ 18 F]Fluoride Elution Techniques for the Enhancement of Copper-Mediated Late-Stage Radiofluorination

One-pot synthesis of high molar activity 6-[ 18 F]fluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor

Mechanistic Investigations of Cu-Catalyzed Fluorination of Diaryliodonium Salts: Elaborating the CuI/CuIII Manifold in Copper Catalysis

Automated synthesis of PET radiotracers by copper‐mediated 18F‐fluorination of organoborons: Importance of the order of addition and competing protodeborylation

Pd-Catalyzed Decarbonylative Cross-Couplings of Aroyl Chlorides

Palladium- and Nickel-Catalyzed Decarbonylative C–S Coupling to Convert Thioesters to Thioethers

Cu-Catalyzed Fluorination of Diaryliodonium Salts with KF

Mechanistic Investigations of Cu-Catalyzed Fluorination of Diaryliodonium Salts: Elaborating the Cu I /Cu III Manifold in Copper Catalysis

Catalytic Sulfamoylation of Alcohols with Activated Aryl Sulfamates

C-H 18F-fluorination of 8-methylquinolines with Ag[18F]FElectronic supplementary information (ESI) available: Experimental procedures, optimization details, radio-HPLC/TLC traces and spectral data. See DOI: 10.1039/c9cc00641a

Synthesis of High Molar Activity [18F]6-Fluoro-L-DOPA Suitable for Human Use by Cu-Mediated Fluorination of a BPin Precursor

C-H 18 F-fluorination of 8-methylquinolines with Ag[ 18 F]F

C–H 18F-fluorination of 8-methylquinolines with Ag[18F]F

Synthesis of [18F]-γ-Fluoro-α,β-unsaturated Esters and Ketones via Vinylogous 18F-Fluorination of α-Diazoacetates with [18F]AgF

One-pot synthesis of high molar activity 6-18Ffluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor

One-pot synthesis of high molar activity 6-[F]fluoro--DOPA by Cu-mediated fluorination of a BPin precursor

Reducing Limitation in Probe Design: The Development of a Diazirine-Compatible Suzuki–Miyaura Cross Coupling Reaction

One-pot synthesis of high molar activity 6-[18F]fluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor

Protecting group free radical C-H trifluoromethylation of peptidesElectronic supplementary information (ESI) available. See DOI: 10.1039/c8sc00368h

Protecting group free radical C–H trifluoromethylation of peptides† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc00368h

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