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Ferryl Protonation in Oxoiron(IV) Porphyrins and Its Role in Oxygen Transfer

Journal of the American Chemical Society, 2015-03, Vol.137 (8), p.2875-2885

2015

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Selective CH Functionalization of Methane, Ethane, and Propane by a Perfluoroarene Iodine(III) Complex

Angewandte Chemie International Edition, 2014-09, Vol.53 (39), p.10490-10494

International ed. in English, 2014

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Mechanism of Hydrocarbon Functionalization by an Iodate/Chloride System: The Role of Ester Protection

ACS catalysis, 2018-04, Vol.8 (4), p.3138-3149

2018

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Selective benzylic C-H monooxygenation mediated by iodine oxides

Beilstein journal of organic chemistry, 2019-03, Vol.15 (1), p.602-609

2019

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Omadacycline dihydrate, C29H40N4O7·2H2O, from X-ray powder diffraction data

Acta crystallographica. Section E, Crystallographic communications, 2024-03, Vol.80 (Pt 3), p.292-295

2024

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Fishing for peroxidase protons

Science (American Association for the Advancement of Science), 2014-07, Vol.345 (6193), p.142-143

2014

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Crystal structure of ractopamine hydrochloride, C18H24NO3Cl

Powder diffraction, 2024-06, Vol.39 (2), p.94-104

2024

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Selective Monooxidation of Light Alkanes Using Chloride and Iodate

Journal of the American Chemical Society, 2014-06, Vol.136 (23), p.8393-8401

2014

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Omadacycline dihydrate, C 29 H 40 N 4 O 7 ·2H 2 O, from X-ray powder diffraction data

Acta crystallographica. Section E, Crystallographic communications, 2024-03, Vol.80 (Pt 3), p.292-295

2024

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Cynarine monohydrate from synchrotron powder X‐ray diffraction data

Acta crystallographica. Section C, Crystal structure communications, 2022-02, Vol.78 (2), p.101-106

2022

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Crystal structure of fulvestrant hydrate (ethyl acetate), C32H47F5O3S(H2O)0.16(C4H8O2)0.025

Powder diffraction, 2022-09, Vol.37 (3), p.157-165

2022

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Selective Photo‐Oxygenation of Light Alkanes Using Iodine Oxides and Chloride

ChemCatChem, 2019-10, Vol.11 (20), p.5045-5054

2019

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Partial oxidation of light alkanes by periodate and chloride salts

Dalton transactions : an international journal of inorganic chemistry, 2015-03, Vol.44 (12), p.5294-5298

2015

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Crystal structure of osimertinib mesylate Form B (Tagrisso), (C28H34N7O2)(CH3O3S)

Powder diffraction, 2021-12, Vol.36 (4), p.282-290

2021

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Crystal structure of ivermectin hemihydrate ethanolate, (C48H74O14)(H2O)0.5(C2H5OH)0.82

Powder diffraction, 2021-12, Vol.36 (4), p.247-256

2021

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Reductive functionalization of a rhodium(III)-methyl bond by electronic modification of the supporting ligand

Dalton transactions : an international journal of inorganic chemistry, 2014-06, Vol.43 (22), p.8273-8281

2014

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Crystal structure of oxybutynin hydrochloride hemihydrate, C22H32NO3Cl(H2O)0.5

Powder diffraction, 2019-03, Vol.34 (1), p.50-58

2019

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Substituent Effects on Keto–Enol Equilibria Using NMR Spectroscopy

Journal of chemical education, 2011-10, Vol.88 (10), p.1444-1445

2011

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Activation of Fmoc-Protected N,O-Acetals Using Trimethylsilyl Halides: Mechanistic and Synthetic Studies

Organic letters, 2010-06, Vol.12 (11), p.2464-2467

2010

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Correction to Substituent Effects on Keto–Enol Equilibria Using NMR Spectroscopy

Journal of chemical education, 2012-02, Vol.89 (3), p.421-421

2012

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Crystal structure of ractopamine hydrochloride, C 18 H 24 NO 3 Cl

Powder diffraction, 2024-06, Vol.39 (2), p.94-104

2024

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X-ray scattering investigation of ion aggregation in imidazolium-based ionic liquids upon doping with lithium, sodium, potassium, rubidium and cesium salts

Journal of molecular liquids, 2020-03, Vol.302, p.112540, Article 112540

2020

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Crystal structures of large-volume commercial pharmaceuticals

Acta crystallographica. Section A, Foundations and advances, 2021-08, Vol.77 (a2), p.C111-C111

2021

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Fishing for peroxidase protons: Where are the protons in heme protein catalysis?

Science (American Association for the Advancement of Science), 2014-07, Vol.345 (6193), p.142-143

2014

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Crystal structure of fulvestrant hydrate (ethyl acetate), C 32 H 47 F 5 O 3 S(H 2 O) 0.16 (C 4 H 8 O 2 ) 0.025

Powder diffraction, 2022-09, Vol.37 (3), p.157-165

2022

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Ferryl Protonation in Oxoiron(IV) Porphyrins and Its Role in Oxygen Transfer

Selective CH Functionalization of Methane, Ethane, and Propane by a Perfluoroarene Iodine(III) Complex

Mechanism of Hydrocarbon Functionalization by an Iodate/Chloride System: The Role of Ester Protection

Selective benzylic C-H monooxygenation mediated by iodine oxides

Omadacycline dihydrate, C29H40N4O7·2H2O, from X-ray powder diffraction data

Fishing for peroxidase protons

Crystal structure of ractopamine hydrochloride, C18H24NO3Cl

Selective Monooxidation of Light Alkanes Using Chloride and Iodate

Omadacycline dihydrate, C 29 H 40 N 4 O 7 ·2H 2 O, from X-ray powder diffraction data

Cynarine monohydrate from synchrotron powder X‐ray diffraction data

Crystal structure of fulvestrant hydrate (ethyl acetate), C32H47F5O3S(H2O)0.16(C4H8O2)0.025

Selective Photo‐Oxygenation of Light Alkanes Using Iodine Oxides and Chloride

Partial oxidation of light alkanes by periodate and chloride salts

Crystal structure of osimertinib mesylate Form B (Tagrisso), (C28H34N7O2)(CH3O3S)

Crystal structure of ivermectin hemihydrate ethanolate, (C48H74O14)(H2O)0.5(C2H5OH)0.82

Reductive functionalization of a rhodium(III)-methyl bond by electronic modification of the supporting ligand

Crystal structure of oxybutynin hydrochloride hemihydrate, C22H32NO3Cl(H2O)0.5

Substituent Effects on Keto–Enol Equilibria Using NMR Spectroscopy

Activation of Fmoc-Protected N,O-Acetals Using Trimethylsilyl Halides: Mechanistic and Synthetic Studies

Correction to Substituent Effects on Keto–Enol Equilibria Using NMR Spectroscopy

Crystal structure of ractopamine hydrochloride, C 18 H 24 NO 3 Cl

X-ray scattering investigation of ion aggregation in imidazolium-based ionic liquids upon doping with lithium, sodium, potassium, rubidium and cesium salts

Crystal structures of large-volume commercial pharmaceuticals

Fishing for peroxidase protons: Where are the protons in heme protein catalysis?

Crystal structure of fulvestrant hydrate (ethyl acetate), C 32 H 47 F 5 O 3 S(H 2 O) 0.16 (C 4 H 8 O 2 ) 0.025

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