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Jan Wiesenthal

Chemiker

Name	Jan Wiesenthal
Ort	Hilden Deutschland
Akademischer Grad bzw. Titel	Dr. rer. nt., M. Sc. RWTH
Beruf	Chemiker (charakteristischer Beruf)
Variante	J. Wiesenthal
Weitere Angaben	Dissertation an der Rheinisch-Westfälischen Technischen Hochschule Aachen, Fakultät für Mathematik, Informatik und Naturwissenschaften, 2023.
Quelle	Dissertation
Datensatztyp	Person
GND-Nummer	1305856279
Datensatz-ID	1305856279
Beteiligt an alle anzeigen Concatenating Microbial, Enzymatic, and Organometallic Catalysis for Integrated Conversion of Renewable Carbon Sources Author Correction: Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol Author Correction : Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol Synthesis of cyclic acetals utilizing homogeneous and immobilized transition metal catalysts Effective Production of Selected Dioxolanes by Sequential Bio‐ and Chemocatalysis Enabled by Adapted Solvent Switching Effective Production of Selected Dioxolanes by Sequential Bio- and Chemocatalysis Enabled by Adapted Solvent Switching Utilization of Formic Acid as C1 Building Block for the Ruthenium‐Catalyzed Synthesis of Formaldehyde Surrogates Utilization of Formic Acid as C1 Building Block for the Ruthenium-Catalyzed Synthesis of Formaldehyde Surrogates Ruthenium‐Catalyzed Synthesis of Dialkoxymethane Ethers Utilizing Carbon Dioxide and Molecular Hydrogen Ruthenium‐Catalyzed Synthesis of Dialkoxymethane Ethers Utilizing Carbon Dioxide and Molecular Hydrogen

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Jan Wiesenthal

Concatenating Microbial, Enzymatic, and Organometallic Catalysis for Integrated Conversion of Renewable Carbon Sources

Author Correction: Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol

Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol

Author Correction : Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol

Interdisciplinary development of an overall process concept from glucose to 4,5-dimethyl-1,3-dioxolane via 2,3-butanediol

Synthesis of cyclic acetals utilizing homogeneous and immobilized transition metal catalysts

Effective Production of Selected Dioxolanes by Sequential Bio‐ and Chemocatalysis Enabled by Adapted Solvent Switching

Effective Production of Selected Dioxolanes by Sequential Bio- and Chemocatalysis Enabled by Adapted Solvent Switching

Utilization of Formic Acid as C1 Building Block for the Ruthenium‐Catalyzed Synthesis of Formaldehyde Surrogates

Utilization of Formic Acid as C1 Building Block for the Ruthenium-Catalyzed Synthesis of Formaldehyde Surrogates

Ruthenium‐Catalyzed Synthesis of Dialkoxymethane Ethers Utilizing Carbon Dioxide and Molecular Hydrogen

Ruthenium‐Catalyzed Synthesis of Dialkoxymethane Ethers Utilizing Carbon Dioxide and Molecular Hydrogen