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Jörg Pietruszka (1965-)

Chemiker

Name	Jörg Pietruszka
Zeit	1965- (Lebensdaten)
Ort	Deutschland
Akademischer Grad bzw. Titel	Dipl.-Chem. Prof. Dr.
Beruf	Chemiker (charakteristischer Beruf) Hochschullehrer
Beziehung	Forschungszentrum Jülich (2013-) Heinrich-Heine-Universität Düsseldorf. Institut für Bioorganische Chemie (2004-) Universität Stuttgart (1995-2004) University of Cambridge (1993-1995) Universität Hamburg (1985-1993)
Weitere Angaben	Seit 2013 Direktor, Biotechnologie (IBG-1), Institut für Bio- und Geowissenschaften (IBG), Forschungszentrum Jülich Seit 2004 Institutsleiter, Institut für Bioorganische Chemie, Heinrich-Heine-Universität Düsseldorf 2001 Habilition, Universität Stuttgart 1993 Promotion, Universität Hamburg 1985-1991 Chemiestudium, Universität Hamburg und Newcastle upon Tyne (UK)
Datensatztyp	Person
GND-Nummer	172656052
Datensatz-ID	172656052
Beteiligt an alle anzeigen From the Total Synthesis of Semi–Viriditoxin, Semi–Viriditoxic Acid and Dimeric Naphthopyranones to their Biological Activities in Burkitt B Cell Lymphoma High‐Throughput Colorimetric Detection and Quantification of Indoles and Pyrroloindoles for Enzymatic Activity Determination Application of cyclic diaryliodonium salts in the synthesis of axially chiral natural product analogues Generation of Cannabigerolic Acid Derivatives and Their Precursors by Using the Promiscuity of the Aromatic Prenyltransferase NphB Atroposelective Total Synthesis of (+)‐Isokotanin A via Combined Metal and Enzyme Catalysis A Common C 2 ‐Symmetric 2,2’‐Biphenol Building Block and its Application in the Synthesis of (+)‐di‐ epi ‐Gonytolide A Synthesis of a Water-Soluble Tridentate (Dimethylamino) ethyl Cu (I)/Cu (II)-Ligand Carrier‐Free Enzyme Immobilizates for Flow Chemistry Enzymatic valorization of sustainable carbon sources Covalently Immobilized 2‐Deoxyribose‐5‐phosphate Aldolase (DERA) for Biocatalysis in Flow: Utilization of the 3‐Hydroxyaldehyde Intermediate in Reaction Cascades Optochemical Control of Bacterial Gene Expression: Novel Photocaged Compounds for Different Promoter Systems Enantioselective Allylation of Cyclic and In Situ Formed N ‐Unsubstituted Imines with Tetraol‐Protected Allylboronates Biokatalytische C3‐Indol‐Methylierung – ein nützliches Werkzeug für die naturstoffinspirierte stereoselektive Synthese von Pyrroloindolen Biocatalytic C3‐Indole Methylation—A Useful Tool for the Natural‐Product‐Inspired Stereoselective Synthesis of Pyrroloindoles Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses Lewis‐Base‐Brønsted‐Säure‐Enzym‐Katalyse in enantioselektiven mehrstufigen Eintopf‐Synthesen Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses Optogenetic control of bio(techno)logical processes in bacteria at different cellular levels Synthesis of the Thomsen-Friedenreich-antigen (TF-antigen) and binding of Galectin-3 to TF-antigen presenting neo-glycoproteins A Fluorescence‐Based Assay System for the Determination of Haloperoxidase‐Activity Using a Two‐Dimensional Calibration Ap‐proach Frontispiece: Exceptional Substrate Diversity in Oxygenation Reactions Catalyzed by a Bis (μ‐oxo) Copper Complex Effect of Photocaged Isopropyl β‐ d ‐1‐thiogalactopyranoside Solubility on the Light Responsiveness of LacI‐controlled Expression Systems in Different Bacteria Experimental and Computational Investigations of the Reactions between α,β‐Unsaturated Lactones and 1,3‐Dienes by Cooperative Lewis Acid/Brønsted Acid Catalysis Cover Picture: Enantioselective Ammonium Ylide Mediated One‐Pot Synthesis of Highly Substituted γ ‐Butyrolactones (Adv. Synth. Catal. 12/2020) Tyrosinases in Organic Chemistry: A Versatile Tool for the α‐Arylation of β‐Dicarbonyl Compounds Enantioselective, Catalytic One‐Pot Synthesis of γ ‐Butyrolactone‐Based Fragrances Preparation of Cyclic Prodiginines by Mutasynthesis in Pseudomonas putida KT2440 Cover Feature: Preparation of Cyclic Prodiginines by Mutasynthesis in Pseudomonas putida KT2440 (ChemBioChem 14/2018) Identification of Stable and Enantioselective Lipases for Biotechnological Applications Highly Enantioselective Allylation of Ketones: An Efficient Approach to All Stereoisomers of Tertiary Homoallylic Alcohols P450 BM3‐Catalyzed Regio‐ and Stereoselective Hydroxylation Aiming at the Synthesis of Phthalides and Isocoumarins Neuartige Synthesen funktioneller π-Systeme auf Basis palladiumkatalysierter Alkinylierungsreaktionen P450 BM3 Monooxygenase as an Efficient NAD (P) H‐Oxidase for Regeneration of Nicotinamide Cofactors in ADH‐Catalysed Preparative Scale Biotransformations Design, synthesis and biological evaluation of rhomboid protease specific inhibitors Etablierung von P450 BM3 Monooxygenasen als chemo- und stereoselektive Biokatalysatoren für die organische Synthese Erratum to: Alternative hosts for functional (meta)genome analysis 2-Steps in 1-pot: enzyme cascades for the synthesis of chiral vicinal amino alcohols Magic-Angle-Spinning Solid-state NMR Studies of the Membrane Binding Heme Protein Nitrophorin 7 (NP7) from Rhodnius prolixus Methodische Erweiterung der Masuda-Borylierungs-Suzuki-Kupplungs-Sequenz Multikomponentensynthese von Oligothiophenen und deren chemoenzymatische Transformation The Metagenome-derived enzymes LipS and LipT increase the diversity of known lipases Crystal structure of ethyl 2,3,4-tri-O-acetyl-1-thio-β-L-rhamnopyranoside, C 14 H 22 O 7 S Crystal structure of ethyl 2,3,4,6-tetra-O-acetyl-1-thio-α-Dmannopyranoside, C 16 H 24 O 9 S Enantiomerically Pure Vinylcyclopropylboronic Esters † Enantiomerenreine Cyclopropane : neue Bausteine für die Natur- und Wirkstoffsynthese Synthese und gaschromatographische Enantiomerentrennung von axial chiralen Allenen

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Katalog der Deutschen Nationalbibliothek

Jörg Pietruszka (1965-)

From the Total Synthesis of Semi–Viriditoxin, Semi–Viriditoxic Acid and Dimeric Naphthopyranones to their Biological Activities in Burkitt B Cell Lymphoma

High‐Throughput Colorimetric Detection and Quantification of Indoles and Pyrroloindoles for Enzymatic Activity Determination

Application of cyclic diaryliodonium salts in the synthesis of axially chiral natural product analogues

Generation of Cannabigerolic Acid Derivatives and Their Precursors by Using the Promiscuity of the Aromatic Prenyltransferase NphB

Atroposelective Total Synthesis of (+)‐Isokotanin A via Combined Metal and Enzyme Catalysis

A Common C 2 ‐Symmetric 2,2’‐Biphenol Building Block and its Application in the Synthesis of (+)‐di‐ epi ‐Gonytolide A

Synthesis of a Water-Soluble Tridentate (Dimethylamino) ethyl Cu (I)/Cu (II)-Ligand

Carrier‐Free Enzyme Immobilizates for Flow Chemistry

Enzymatic valorization of sustainable carbon sources

Covalently Immobilized 2‐Deoxyribose‐5‐phosphate Aldolase (DERA) for Biocatalysis in Flow: Utilization of the 3‐Hydroxyaldehyde Intermediate in Reaction Cascades

Optochemical Control of Bacterial Gene Expression: Novel Photocaged Compounds for Different Promoter Systems

Enantioselective Allylation of Cyclic and In Situ Formed N ‐Unsubstituted Imines with Tetraol‐Protected Allylboronates

Biokatalytische C3‐Indol‐Methylierung – ein nützliches Werkzeug für die naturstoffinspirierte stereoselektive Synthese von Pyrroloindolen

Biocatalytic C3‐Indole Methylation—A Useful Tool for the Natural‐Product‐Inspired Stereoselective Synthesis of Pyrroloindoles

Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses

Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses

Lewis‐Base‐Brønsted‐Säure‐Enzym‐Katalyse in enantioselektiven mehrstufigen Eintopf‐Synthesen

Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses

Optogenetic control of bio(techno)logical processes in bacteria at different cellular levels

Synthesis of the Thomsen-Friedenreich-antigen (TF-antigen) and binding of Galectin-3 to TF-antigen presenting neo-glycoproteins

A Fluorescence‐Based Assay System for the Determination of Haloperoxidase‐Activity Using a Two‐Dimensional Calibration Ap‐proach

Frontispiece: Exceptional Substrate Diversity in Oxygenation Reactions Catalyzed by a Bis (μ‐oxo) Copper Complex

Effect of Photocaged Isopropyl β‐ d ‐1‐thiogalactopyranoside Solubility on the Light Responsiveness of LacI‐controlled Expression Systems in Different Bacteria

Experimental and Computational Investigations of the Reactions between α,β‐Unsaturated Lactones and 1,3‐Dienes by Cooperative Lewis Acid/Brønsted Acid Catalysis

Cover Picture: Enantioselective Ammonium Ylide Mediated One‐Pot Synthesis of Highly Substituted γ ‐Butyrolactones (Adv. Synth. Catal. 12/2020)

Tyrosinases in Organic Chemistry: A Versatile Tool for the α‐Arylation of β‐Dicarbonyl Compounds

Enantioselective, Catalytic One‐Pot Synthesis of γ ‐Butyrolactone‐Based Fragrances

Preparation of Cyclic Prodiginines by Mutasynthesis in Pseudomonas putida KT2440

Cover Feature: Preparation of Cyclic Prodiginines by Mutasynthesis in Pseudomonas putida KT2440 (ChemBioChem 14/2018)

Identification of Stable and Enantioselective Lipases for Biotechnological Applications

Highly Enantioselective Allylation of Ketones: An Efficient Approach to All Stereoisomers of Tertiary Homoallylic Alcohols

P450 BM3‐Catalyzed Regio‐ and Stereoselective Hydroxylation Aiming at the Synthesis of Phthalides and Isocoumarins

Neuartige Synthesen funktioneller π-Systeme auf Basis palladiumkatalysierter Alkinylierungsreaktionen

P450 BM3 Monooxygenase as an Efficient NAD (P) H‐Oxidase for Regeneration of Nicotinamide Cofactors in ADH‐Catalysed Preparative Scale Biotransformations

Design, synthesis and biological evaluation of rhomboid protease specific inhibitors

Etablierung von P450 BM3 Monooxygenasen als chemo- und stereoselektive Biokatalysatoren für die organische Synthese

Erratum to: Alternative hosts for functional (meta)genome analysis

2-Steps in 1-pot: enzyme cascades for the synthesis of chiral vicinal amino alcohols

Magic-Angle-Spinning Solid-state NMR Studies of the Membrane Binding Heme Protein Nitrophorin 7 (NP7) from Rhodnius prolixus

Methodische Erweiterung der Masuda-Borylierungs-Suzuki-Kupplungs-Sequenz

Multikomponentensynthese von Oligothiophenen und deren chemoenzymatische Transformation

The Metagenome-derived enzymes LipS and LipT increase the diversity of known lipases

Crystal structure of ethyl 2,3,4-tri-O-acetyl-1-thio-β-L-rhamnopyranoside, C 14 H 22 O 7 S

Crystal structure of ethyl 2,3,4,6-tetra-O-acetyl-1-thio-α-Dmannopyranoside, C 16 H 24 O 9 S

Enantiomerically Pure Vinylcyclopropylboronic Esters †

Enantiomerenreine Cyclopropane : neue Bausteine für die Natur- und Wirkstoffsynthese

Synthese und gaschromatographische Enantiomerentrennung von axial chiralen Allenen