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The (Not So) Ephemeral Trifluoromethanide Anion

Angewandte Chemie (International ed.), 2014-10, Vol.53 (43), p.11414-11415

International ed. in English, 2014

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Rate of single electron reduction of Togni’s reagent

Journal of fluorine chemistry, 2017-11, Vol.203, p.218-222

2017

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Accessing N-Stereogenicity through a Double Aza-Michael Reaction: Mechanistic Insights

Chemistry : a European journal, 2016-01, Vol.22 (1), p.390-403

2016

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Making the SF5 Group More Accessible: A Gas‐Reagent‐Free Approach to Aryl Tetrafluoro‐λ6‐sulfanyl Chlorides

Angewandte Chemie International Edition, 2019-02, Vol.58 (7), p.1950-1954

International ed. in English, 2019

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Hypervalent Iodine-based Trifluoromethylating Agents Made in Switzerland

Chimia, 2014-01, Vol.68 (6), p.419

2014

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Determining the predominant tautomeric structure of iodine-based group-transfer reagents by 17O NMR spectroscopy

Beilstein journal of organic chemistry, 2018-01, Vol.14 (1), p.2289-2294

2018

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An Experimental Radical Electrophilicity Index

Chemphyschem, 2017-11, Vol.18 (21), p.2973-2976

2017

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Quantitative Profiling of the Heavy‐Atom Effect in BODIPY Dyes: Correlating Initial Rates, Atomic Numbers, and 1O2 Quantum Yields

European journal of organic chemistry, 2017-04, Vol.2017 (15), p.2170-2178

2017

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A Janus cyclohexane ring

Nature chemistry, 2015-06, Vol.7 (6), p.467-468

2015

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Electrophilic Trifluoromethylation of S-Hydrogen Phosphorothioates

Journal of organic chemistry, 2011-05, Vol.76 (10), p.4189-4193

2011

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Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH → F] Substitution in d-Glucose and d-Galactose

European journal of organic chemistry, 2015-11, Vol.2015 (32), p.6983-6987

2015

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Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH[arrow right]F] Substitution in d-Glucose and d-Galactose

European journal of organic chemistry, 2015-11, Vol.2015 (32), p.6983

2015

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Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH → F] Substitution in d-Glucose and d-Galactose (Eur. J. Org. Chem. 32/2015)

European journal of organic chemistry, 2015-11, Vol.2015 (32), p.n/a

2015

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Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH[arrow right]F] Substitution in d-Glucose and d-Galactose

European journal of organic chemistry, 2015-11, Vol.2015 (32)

2015

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Synthesis, characterization and initial evaluation of 5-nitro-1-(trifluoromethyl)-3H-1λ3,2-benziodaoxol-3-one

Beilstein journal of organic chemistry, 2014-01, Vol.10 (1), p.1-6

2014

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Das (nicht so) kurzlebige Trifluormethylanion

Angewandte Chemie, 2014-10, Vol.126 (43), p.11598-11599

2014

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Mechanistic insight into the thermal activation of Togni's trifluoromethylation reagentsDedicated to Prof. Antonio Togni on account of receiving the 2017 ACS National Award for Creative Work in Fluorine Chemistry.Electronic supplementary information (ESI) available. See DOI: 10.1039/c7cp01396e

2017-07

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Profiling the oxidative activation of DMSO-F by pulse radiolysis and translational potential for radical C-H trifluoromethylation

Organic & biomolecular chemistry, 2019-11, Vol.17 (45), p.9734-9742

2019

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Mechanistic insight into the thermal activation of Togni's trifluoromethylation reagents

Physical chemistry chemical physics : PCCP, 2017, Vol.19 (28), p.18172-18177

2017

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Profiling the oxidative activation of DMSO-F 6 by pulse radiolysis and translational potential for radical C-H trifluoromethylation

Organic & biomolecular chemistry, 2019-12, Vol.17 (45), p.9734-9742

2019

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Making the SF 5 Group More Accessible: A Gas-Reagent-Free Approach to Aryl Tetrafluoro-λ 6 -sulfanyl Chlorides

Angewandte Chemie International Edition, 2019-02, Vol.58 (7), p.1950-1954

2019

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Trifluoromethyl Derivatives of Benzooxatellurole

Helvetica chimica acta, 2019-06, Vol.102 (6), p.n/a

2019

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Die SF5‐Gruppe zugänglicher gemacht: Eine gasfreie Synthese von Aryl‐Tetrafluor‐λ6‐Sulfanyl‐Chloriden

Angewandte Chemie, 2019-02, Vol.131 (7), p.1970-1974

2019

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S-Trifluoromethylation of Thiols by Hypervalent Iodine Reagents: A Joint Experimental and Computational Study

Chemistry : a European journal, 2016-01, Vol.22 (5), p.1704-1713

2016

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Profiling the oxidative activation of DMSO-F6 by pulse radiolysis and translational potential for radical C–H trifluoromethylation

Organic & biomolecular chemistry, 2019, Vol.17 (45), p.9734-9742

2019

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The (Not So) Ephemeral Trifluoromethanide Anion

Rate of single electron reduction of Togni’s reagent

Accessing N-Stereogenicity through a Double Aza-Michael Reaction: Mechanistic Insights

Making the SF5 Group More Accessible: A Gas‐Reagent‐Free Approach to Aryl Tetrafluoro‐λ6‐sulfanyl Chlorides

Hypervalent Iodine-based Trifluoromethylating Agents Made in Switzerland

Determining the predominant tautomeric structure of iodine-based group-transfer reagents by 17O NMR spectroscopy

An Experimental Radical Electrophilicity Index

Quantitative Profiling of the Heavy‐Atom Effect in BODIPY Dyes: Correlating Initial Rates, Atomic Numbers, and 1O2 Quantum Yields

A Janus cyclohexane ring

Electrophilic Trifluoromethylation of S-Hydrogen Phosphorothioates

Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH → F] Substitution in d-Glucose and d-Galactose

Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH[arrow right]F] Substitution in d-Glucose and d-Galactose

Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH → F] Substitution in d-Glucose and d-Galactose (Eur. J. Org. Chem. 32/2015)

Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH[arrow right]F] Substitution in d-Glucose and d-Galactose

Synthesis, characterization and initial evaluation of 5-nitro-1-(trifluoromethyl)-3H-1λ3,2-benziodaoxol-3-one

Das (nicht so) kurzlebige Trifluormethylanion

Mechanistic insight into the thermal activation of Togni's trifluoromethylation reagentsDedicated to Prof. Antonio Togni on account of receiving the 2017 ACS National Award for Creative Work in Fluorine Chemistry.Electronic supplementary information (ESI) available. See DOI: 10.1039/c7cp01396e

Profiling the oxidative activation of DMSO-F by pulse radiolysis and translational potential for radical C-H trifluoromethylation

Mechanistic insight into the thermal activation of Togni's trifluoromethylation reagents

Profiling the oxidative activation of DMSO-F 6 by pulse radiolysis and translational potential for radical C-H trifluoromethylation

Making the SF 5 Group More Accessible: A Gas-Reagent-Free Approach to Aryl Tetrafluoro-λ 6 -sulfanyl Chlorides

Trifluoromethyl Derivatives of Benzooxatellurole

Die SF5‐Gruppe zugänglicher gemacht: Eine gasfreie Synthese von Aryl‐Tetrafluor‐λ6‐Sulfanyl‐Chloriden

S-Trifluoromethylation of Thiols by Hypervalent Iodine Reagents: A Joint Experimental and Computational Study

Profiling the oxidative activation of DMSO-F6 by pulse radiolysis and translational potential for radical C–H trifluoromethylation

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