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Photoredox Generation of Carbon‐Centered Radicals Enables the Construction of 1,1‐Difluoroalkene Carbonyl Mimics

Angewandte Chemie International Edition, 2017-11, Vol.56 (47), p.15073-15077

International ed. in English, 2017

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Photoredox-Mediated Routes to Radicals: The Value of Catalytic Radical Generation in Synthetic Methods Development

ACS catalysis, 2017-04, Vol.7 (4), p.2563-2575

2017

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Open-Air Alkylation Reactions in Photoredox-Catalyzed DNA-Encoded Library Synthesis

Journal of the American Chemical Society, 2019-02, Vol.141 (8), p.3723-3732

2019

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Redox-Neutral Photocatalytic Cyclopropanation via Radical/Polar Crossover

Journal of the American Chemical Society, 2018-06, Vol.140 (25), p.8037-8047

2018

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Decarboxylative Allylation of Amino Alkanoic Acids and Esters via Dual Catalysis

Journal of the American Chemical Society, 2014-10, Vol.136 (39), p.13606-13609

2014

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A General One-Pot Protocol for Hindered N -Alkyl Azaheterocycles from Tertiary Carboxylic Acids

Organic letters, 2020-06, Vol.22 (11), p.4180-4184

2020

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Photocatalytic Aminodecarboxylation of Carboxylic Acids

European journal of organic chemistry, 2016-07, Vol.2016 (20), p.3331-3334

2016

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Nickel-Catalyzed Antibody Bioconjugation

Journal of the American Chemical Society, 2023-11, Vol.145 (47), p.25842-25849

2023

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Photoinduced Kochi Decarboxylative Elimination for the Synthesis of Enamides and Enecarbamates from N‑Acyl Amino Acids

Journal of organic chemistry, 2019-03, Vol.84 (5), p.2933-2940

2019

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Dual Catalytic Decarboxylative Allylations of α-Amino Acids and Their Divergent Mechanisms

Chemistry : a European journal, 2015-12, Vol.21 (51), p.18589-18593

2015

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Activation of Alcohols with Carbon Dioxide: Intermolecular Allylation of Weakly Acidic Pronucleophiles

Organic letters, 2014-08, Vol.16 (16), p.4308-4311

2014

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Design and Optimization of Selectivity-Tunable Toll-like Receptor 7/8 Agonists as Novel Antibody-Drug Conjugate Payloads

Journal of medicinal chemistry, 2024-09, Vol.67 (17), p.15756-15779

2024

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Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies

Chemical science (Cambridge), 2018-03, Vol.9 (12), p.3215-3220

2018

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Development of Asymmetric Deacylative Allylation

Journal of organic chemistry, 2013-07, Vol.78 (14), p.7281-7287

2013

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Correction: Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies

Chemical science (Cambridge), 2018-06, Vol.9 (22), p.5119-5119

2018

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Engaging sulfinate salts via Ni/photoredox dual catalysis enables facile Csp2–SO2R coupling

Chemical science (Cambridge), 2018-01, Vol.9 (12), p.3186-3191

2018

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A Diels–Alder/Ene Cascade Leading to 5‐(Pyrrolidin‐3‐yl)thieno[3,2‐e]isoindoles from Ketone‐derived 2‐Vinylthiophenes and N‐Phenylmaleimide

Journal of heterocyclic chemistry, 2018-12, Vol.55 (12), p.2698-2714

2018

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Photoredox Generation of Carbon‐Centered Radicals Enables the Construction of 1,1‐Difluoroalkene Carbonyl Mimics

Angewandte Chemie, 2017-11, Vol.129 (47), p.15269-15273

2017

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Crystal structure of (1 S ,2 R ,6 R ,7 R ,8 S ,12 S )-4,10,17-triphenyl-15-thia-4,10-diazapentacyclo[5.5.5.0 1,16 .0 2,6 .0 8,12 ]heptadeca-13,16-diene-3,5,9,11-tetrone p -xylene hemisolvate

Acta crystallographica. Section E, Structure reports online, 2014-12, Vol.70 (12), p.550-554

2014

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Photoredox Enables the Construction of 1,1-Difluoroalkene Carbonyl Mimics

Angewandte Chemie International Edition, 2017-10, Vol.56 (47), p.15073-15077

2017

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Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategiesElectronic supplementary information (ESI) available. CCDC 1811877, 1817386-1817390. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc05420c

2018-03

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Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies† †Electronic supplementary information (ESI) available. CCDC 1811877, 1817386–1817390. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc05420c

Chemical science (Cambridge), 2018-02, Vol.9 (12), p.3215-3220

2018

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Engaging sulfinate salts via Ni/photoredox dual catalysis enables facile C sp 2 -SO 2 R coupling

Chemical science (Cambridge), 2018-03, Vol.9 (12), p.3186

2018

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Engaging sulfinate salts via Ni/photoredox dual catalysis enables facile Csp2-SO2R couplingElectronic supplementary information (ESI) available: Experimental procedures, characterization data for all new products, copies of NMR spectra, Cartesian coordinates for computational data. See DOI: 10.1039/c7sc05402e

2018-03

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Engaging sulfinate salts via Ni/photoredox dual catalysis enables facile Csp2–SO2R coupling† †Electronic supplementary information (ESI) available: Experimental procedures, characterization data for all new products, copies of NMR spectra, Cartesian coordinates for computational data. See DOI: 10.1039/c7sc05402e

Chemical science (Cambridge), 2018-02, Vol.9 (12), p.3186-3191

2018

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Photoredox Generation of Carbon‐Centered Radicals Enables the Construction of 1,1‐Difluoroalkene Carbonyl Mimics

Photoredox-Mediated Routes to Radicals: The Value of Catalytic Radical Generation in Synthetic Methods Development

Open-Air Alkylation Reactions in Photoredox-Catalyzed DNA-Encoded Library Synthesis

Redox-Neutral Photocatalytic Cyclopropanation via Radical/Polar Crossover

Decarboxylative Allylation of Amino Alkanoic Acids and Esters via Dual Catalysis

A General One-Pot Protocol for Hindered N -Alkyl Azaheterocycles from Tertiary Carboxylic Acids

Photocatalytic Aminodecarboxylation of Carboxylic Acids

Nickel-Catalyzed Antibody Bioconjugation

Photoinduced Kochi Decarboxylative Elimination for the Synthesis of Enamides and Enecarbamates from N‑Acyl Amino Acids

Dual Catalytic Decarboxylative Allylations of α-Amino Acids and Their Divergent Mechanisms

Activation of Alcohols with Carbon Dioxide: Intermolecular Allylation of Weakly Acidic Pronucleophiles

Design and Optimization of Selectivity-Tunable Toll-like Receptor 7/8 Agonists as Novel Antibody-Drug Conjugate Payloads

Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies

Development of Asymmetric Deacylative Allylation

Correction: Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies

Engaging sulfinate salts via Ni/photoredox dual catalysis enables facile Csp2–SO2R coupling

A Diels–Alder/Ene Cascade Leading to 5‐(Pyrrolidin‐3‐yl)thieno[3,2‐e]isoindoles from Ketone‐derived 2‐Vinylthiophenes and N‐Phenylmaleimide

Photoredox Generation of Carbon‐Centered Radicals Enables the Construction of 1,1‐Difluoroalkene Carbonyl Mimics

Crystal structure of (1 S ,2 R ,6 R ,7 R ,8 S ,12 S )-4,10,17-triphenyl-15-thia-4,10-diazapentacyclo[5.5.5.0 1,16 .0 2,6 .0 8,12 ]heptadeca-13,16-diene-3,5,9,11-tetrone p -xylene hemisolvate

Photoredox Enables the Construction of 1,1-Difluoroalkene Carbonyl Mimics

Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategiesElectronic supplementary information (ESI) available. CCDC 1811877, 1817386-1817390. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc05420c

Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies† †Electronic supplementary information (ESI) available. CCDC 1811877, 1817386–1817390. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc05420c

Engaging sulfinate salts via Ni/photoredox dual catalysis enables facile C sp 2 -SO 2 R coupling

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