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Analysis of inositol phosphate metabolism by capillary electrophoresis electrospray ionization mass spectrometry

Nature communications, 2020-11, Vol.11 (1), p.6035-12, Article 6035

2020

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Synthesis of Bridged Benzazocines and Benzoxocines by a Titanium-Catalyzed Double-Reductive Umpolung Strategy

Chemistry : a European journal, 2015-02, Vol.21 (6), p.2339-2342

2015

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Synthesis of Modified Nucleoside Oligophosphates Simplified: Fast, Pure, and Protecting Group Free

Journal of the American Chemical Society, 2019-09, Vol.141 (38), p.15013-15017

2019

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The Aryne Phosphate Reaction

Angewandte Chemie (International ed.), 2022-01, Vol.61 (1), p.e202113231-n/a

International ed. in English, 2022

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Lost in Condensation: Poly‑, Cyclo‑, and Ultraphosphates

Accounts of chemical research, 2021-11, Vol.54 (21), p.4036-4050

2021

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Direct conjugate alkylation of α,β-unsaturated carbonyls by Ti(III)-catalysed reductive umpolung of simple activated alkenes

Organic & biomolecular chemistry, 2016-06, Vol.14 (24), p.5673-5682

2016

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Four Phosphates at One Blow: Access to Pentaphosphorylated Magic Spot Nucleotides and Their Analysis by Capillary Electrophoresis

Journal of organic chemistry, 2020-11, Vol.85 (22), p.14496-14506

2020

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Photoaffinity Capture Compounds to Profile the Magic Spot Nucleotide Interactomes

Angewandte Chemie (International ed.), 2022-05, Vol.61 (22), p.e202201731-n/a

International ed. in English, 2022

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Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites

Angewandte Chemie (International ed.), 2022-01, Vol.61 (5), p.n/a

International ed. in English, 2022

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Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O-Phosphoramidites

Angewandte Chemie International Edition, 2022-01, Vol.61 (5), p.e202112457

2022

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Magic spot nucleotides: tunable target-specific chemoenzymatic synthesis

Chemical communications (Cambridge, England), 2019-05, Vol.55 (37), p.5339-5342

2019

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Correction to “Synthesis of Modified Nucleoside Oligophosphates Simplified: Fast, Pure, and Protecting Group Free”

Journal of the American Chemical Society, 2019-10, Vol.141 (41), p.16513-16513

2019

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The Aryne Phosphate Reaction

Angewandte Chemie, 2022-01, Vol.134 (1), p.n/a

2022

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Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites

Angewandte Chemie, 2022-01, Vol.134 (5), p.e202112457-n/a

2022

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Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O-Phosphoramidites

Angewandte Chemie, 2022-01, Vol.134 (5), p.e202112457

2022

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Innentitelbild: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites (Angew. Chem. 5/2022)

Angewandte Chemie, 2022-01, Vol.134 (5), p.n/a

2022

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Photoaffinity Capture Compounds to Profile the Magic Spot Nucleotide Interactomes

Angewandte Chemie, 2022-05, Vol.134 (22), p.n/a

2022

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Direct conjugate alkylation of α,β-unsaturated carbonyls by Ti III -catalysed reductive umpolung of simple activated alkenes

Organic & biomolecular chemistry, 2016, Vol.14 (24), p.5673-5682

2016

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Inside Cover: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites (Angew. Chem. Int. Ed. 5/2022)

Angewandte Chemie International Edition, 2022-01, Vol.61 (5), p.n/a

2022

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Inside Cover: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites (Angew. Chem. Int. Ed. 5/2022)

Angewandte Chemie International Edition, 2022-01, Vol.61 (5)

2022

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Direct conjugate alkylation of α,β-unsaturated carbonyls by TiIII-catalysed reductive umpolung of simple activated alkenesElectronic supplementary information (ESI) available: Additional screening tables, experimental and computational details, characterisation data and NMR spectra of new compounds. CCDC 1440298 and 1440299. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ob02631h

2016-06

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Direct conjugate alkylation of alpha , beta -unsaturated carbonyls by Ti super(III)-catalysed reductive umpolung of simple activated alkenes

Organic & biomolecular chemistry, 2016-06, Vol.14 (24), p.5673-5682

2016

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Magic spot nucleotides: tunable target-specific chemoenzymatic synthesisElectronic supplementary information (ESI) available: Detailed synthetic procedures, characterization data and PAGE - analysis. See DOI: 10.1039/c9cc01688k

2019-05

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Innentitelbild: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites (Angew. Chem. 5/2022)

Angewandte Chemie, 2022-01, Vol.134 (5)

2022

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Bleeding Dieulafoy lesions of the small bowel: a systematic study on the epidemiology and efficacy of enteroscopic treatment

Gastrointestinal endoscopy, 2011-09, Vol.74 (3), p.573-580

2011

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Analysis of inositol phosphate metabolism by capillary electrophoresis electrospray ionization mass spectrometry

Synthesis of Bridged Benzazocines and Benzoxocines by a Titanium-Catalyzed Double-Reductive Umpolung Strategy

Synthesis of Modified Nucleoside Oligophosphates Simplified: Fast, Pure, and Protecting Group Free

The Aryne Phosphate Reaction

Lost in Condensation: Poly‑, Cyclo‑, and Ultraphosphates

Direct conjugate alkylation of α,β-unsaturated carbonyls by Ti(III)-catalysed reductive umpolung of simple activated alkenes

Four Phosphates at One Blow: Access to Pentaphosphorylated Magic Spot Nucleotides and Their Analysis by Capillary Electrophoresis

Photoaffinity Capture Compounds to Profile the Magic Spot Nucleotide Interactomes

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O-Phosphoramidites

Magic spot nucleotides: tunable target-specific chemoenzymatic synthesis

Correction to “Synthesis of Modified Nucleoside Oligophosphates Simplified: Fast, Pure, and Protecting Group Free”

The Aryne Phosphate Reaction

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O-Phosphoramidites

Innentitelbild: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites (Angew. Chem. 5/2022)

Photoaffinity Capture Compounds to Profile the Magic Spot Nucleotide Interactomes

Direct conjugate alkylation of α,β-unsaturated carbonyls by Ti III -catalysed reductive umpolung of simple activated alkenes

Inside Cover: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18O‐Phosphoramidites (Angew. Chem. Int. Ed. 5/2022)

Inside Cover: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites (Angew. Chem. Int. Ed. 5/2022)

Direct conjugate alkylation of alpha , beta -unsaturated carbonyls by Ti super(III)-catalysed reductive umpolung of simple activated alkenes

Magic spot nucleotides: tunable target-specific chemoenzymatic synthesisElectronic supplementary information (ESI) available: Detailed synthetic procedures, characterization data and PAGE - analysis. See DOI: 10.1039/c9cc01688k

Innentitelbild: Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites (Angew. Chem. 5/2022)

Bleeding Dieulafoy lesions of the small bowel: a systematic study on the epidemiology and efficacy of enteroscopic treatment

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