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Thomas Schaub (1980-)

Chemiker

Name	Thomas Schaub
Zeit	1980- (Lebensdaten)
Ort	Deutschland
Akademischer Grad bzw. Titel	Dr. (Universität Karlsruhe) (2006)
Beruf	Chemiker (charakteristischer Beruf)
Beziehung	CarLa (Heidelberg) (2014-) BASF SE (2008-2014)
Weitere Angaben	Diss. Fakultät für Chemie und Biowissenschaften an der Universität Karlsruhe 2006; Seit 2014 Laborleiter des " Catalysis Research Laboratory in Heidelberg"; Referent für Presse- und Öffentlichkeitsarbeit der Vereinigung der Pfälzer Kletterer, Neustadt, Weinstraße
Datensatztyp	Person
GND-Nummer	132888343
Datensatz-ID	132888343
Beteiligt an alle anzeigen Copper (II)‐Catalyzed Amination of Aryl Chlorides in Aqueous Ammonia H 2 Pressure Dependence in the Homogeneously Catalyzed Guerbet Reaction of Ethanol to Butanol using Mn (I) and Ru (II) Mn (III) O^N^O Complexes as Water‐tolerant and Environmentally Benign Catalysts for Polyurethane Foam Synthesis An Organocatalytic Route to endo ‐Vinylene Carbonates from Carbon Dioxide‐Based exo ‐Vinylene Carbonates Synthesis of Anilides by Aminolysis of Unactivated Esters using MnCl 2 in Combination with strong Bases as Catalyst Synthesis of 1,2‐Dialkylaminoethers via Photoredox Catalyzed Hydroamination of Vinylethers Ligand Backbone Influence on the Enantioselectivity in the Ruthenium‐Catalyzed Direct Asymmetric Reductive Amination of Ketones with NH 3/H 2 Using Binaphthyl‐Substituted Phosphines Triflic‐Acid‐Catalyzed Friedel‐Crafts Reaction for the Synthesis of Diaryl Sulfones Copper‐Catalysed Synthesis of Propargyl Alcohol and Derivatives from Acetylene and other Terminal Alkynes Manganese‐Catalyzed Hydrogenation of Sclareolide to Ambradiol Hydrogenative Depolymerization of Polyurethanes Catalyzed by a Manganese Pincer Complex Efficient Industrial Organic Synthesis and the Principles of Green Chemistry Liquid‐liquid‐phase Synthesis of exo ‐Vinylene Carbonates from Primary Propargylic Alcohols: Catalyst Design and Recycling Selektive und skalierbare Synthese von Zuckeralkoholen durch homogene asymmetrische Hydrierung von ungeschützten Ketosen Ruthenium Catalyzed Direct Asymmetric Reductive Amination of Simple Aliphatic Ketones Using Ammonium Iodide and Hydrogen Depolymerization of Technical‐Grade Polyamide 66 and Polyurethane Materials through Hydrogenation Ruthenium‐Catalyzed Deaminative Hydrogenation of Amino Nitriles: Direct Access to 1,2‐Amino Alcohols Direct Photoassisted α‐Trifluoromethylation of Aromatic Ketones with Trifluoroacetic Anhydride (TFAA) Hydrogen Storage : Based on Hydrogenation and Dehydrogenation Reactions of Small Molecules Photoinduced Direct Conversion of Cyclohexane into Cyclohexanone Oxime using LEDs Ruthenium‐Catalyzed Deaminative Hydrogenation of Aliphatic and Aromatic Nitriles to Primary Alcohols Enhanced Activity and Recyclability of Palladium Complexes in the Catalytic Synthesis of Sodium Acrylate from Carbon Dioxide and Ethylene Synthesis of Industrially Relevant Carbamates towards Isocyanates using Carbon Dioxide and Organotin (IV) Alkoxides Direct Synthesis of Primary Amines via Ruthenium‐Catalysed Amination of Ketones with Ammonia and Hydrogen Palladium‐ and Nickel‐Catalyzed Synthesis of Sodium Acrylate from Ethylene, CO 2, and Phenolate Bases: Optimization of the Catalytic System for a Potential Process Neuartige Nickel-Carbenkomplexe und deren Anwendung in Element-Element-Aktivierungsreaktionen

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Thomas Schaub (1980-)

Copper (II)‐Catalyzed Amination of Aryl Chlorides in Aqueous Ammonia

H 2 Pressure Dependence in the Homogeneously Catalyzed Guerbet Reaction of Ethanol to Butanol using Mn (I) and Ru (II)

Mn (III) O^N^O Complexes as Water‐tolerant and Environmentally Benign Catalysts for Polyurethane Foam Synthesis

An Organocatalytic Route to endo ‐Vinylene Carbonates from Carbon Dioxide‐Based exo ‐Vinylene Carbonates

Synthesis of Anilides by Aminolysis of Unactivated Esters using MnCl 2 in Combination with strong Bases as Catalyst

Synthesis of 1,2‐Dialkylaminoethers via Photoredox Catalyzed Hydroamination of Vinylethers

Ligand Backbone Influence on the Enantioselectivity in the Ruthenium‐Catalyzed Direct Asymmetric Reductive Amination of Ketones with NH 3/H 2 Using Binaphthyl‐Substituted Phosphines

Triflic‐Acid‐Catalyzed Friedel‐Crafts Reaction for the Synthesis of Diaryl Sulfones

Copper‐Catalysed Synthesis of Propargyl Alcohol and Derivatives from Acetylene and other Terminal Alkynes

Manganese‐Catalyzed Hydrogenation of Sclareolide to Ambradiol

Hydrogenative Depolymerization of Polyurethanes Catalyzed by a Manganese Pincer Complex

Efficient Industrial Organic Synthesis and the Principles of Green Chemistry

Liquid‐liquid‐phase Synthesis of exo ‐Vinylene Carbonates from Primary Propargylic Alcohols: Catalyst Design and Recycling

Selektive und skalierbare Synthese von Zuckeralkoholen durch homogene asymmetrische Hydrierung von ungeschützten Ketosen

Ruthenium Catalyzed Direct Asymmetric Reductive Amination of Simple Aliphatic Ketones Using Ammonium Iodide and Hydrogen

Depolymerization of Technical‐Grade Polyamide 66 and Polyurethane Materials through Hydrogenation

Ruthenium‐Catalyzed Deaminative Hydrogenation of Amino Nitriles: Direct Access to 1,2‐Amino Alcohols

Direct Photoassisted α‐Trifluoromethylation of Aromatic Ketones with Trifluoroacetic Anhydride (TFAA)

Hydrogen Storage : Based on Hydrogenation and Dehydrogenation Reactions of Small Molecules

Photoinduced Direct Conversion of Cyclohexane into Cyclohexanone Oxime using LEDs

Ruthenium‐Catalyzed Deaminative Hydrogenation of Aliphatic and Aromatic Nitriles to Primary Alcohols

Enhanced Activity and Recyclability of Palladium Complexes in the Catalytic Synthesis of Sodium Acrylate from Carbon Dioxide and Ethylene

Synthesis of Industrially Relevant Carbamates towards Isocyanates using Carbon Dioxide and Organotin (IV) Alkoxides

Direct Synthesis of Primary Amines via Ruthenium‐Catalysed Amination of Ketones with Ammonia and Hydrogen

Palladium‐ and Nickel‐Catalyzed Synthesis of Sodium Acrylate from Ethylene, CO 2, and Phenolate Bases: Optimization of the Catalytic System for a Potential Process

Neuartige Nickel-Carbenkomplexe und deren Anwendung in Element-Element-Aktivierungsreaktionen