Thomas J. J. Müller

Professor (W3)

Heinrich Heine Universität Düsseldorf Mathematisch-Naturwissenschaftliche Fakultät

Germany

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Professor Thomas J. J. Müller is a faculty member at Heinrich Heine Universität Düsseldorf's Mathematisch-Naturwissenschaftliche Fakultät in Germany. His research focuses on recent advances in synthetic methodologies, particularly in the areas of Ene reactions, luminescent materials, and heterocycle synthesis. He has contributed to notable publications addressing the synthesis and application of novel compounds in medicinal chemistry and plant immunity.

Thomas J. J. Müller

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Articles (20)

Recent Advances in Ene Reactions with Carbon Enophiles

Ester‐Aroyl‐S,N‐Ketene Acetals with Solid‐State Luminescence: AIEgens from Sequential Three‐Component Desymmetrization

Bis[1]benzothieno[1,4]thiazine‐S‐oxides–Luminescence of the Anti‐Anti‐Regioisomer

Correction: Kornet, M.M.; Müller, T.J.J. Recent Advances in Sequentially Pd-Catalyzed One-Pot Syntheses of Heterocycles. Molecules 2024, 29, 5265

Concise Four‐Component Synthesis of Solid‐State Fluorescent α‐Sulfenylated Enaminones

Recent Advances in the Synthesis of Substituted Polyacetylenes

In-depth analysis of isochorismate synthase-derived metabolism in plant immunity: Identification of meta-substituted benzoates and salicyloyl-malate

Novel 4-alkoxy Meriolin Congeners Potently Induce Apoptosis in Leukemia and Lymphoma Cells

Recent Advances in Sequentially Pd-Catalyzed One-Pot Syntheses of Heterocycles

Multicomponent syntheses of pyrazoles via (3 + 2)-cyclocondensation and (3 + 2)-cycloaddition key steps

Front Cover: Highly Luminescent Blue Emitter with Balanced Hybridized Locally and Charge‐Transfer Excited‐States Emission (ChemPhotoChem 3/2023)

3‐Ligated Phenothiazinyl‐terephthalonitrile Dyads and Triads ‐ Synthesis, Electronic Properties, Delayed Fluorescence and Electronic Structure

Aggregation‐Induced Emission‐Active Donor‐Substituted Aroyl‐S,N‐Ketene Acetals via Nucleophilic Amine Base Attack

Consecutive four-component synthesis of trisubstituted 3-iodoindoles by an alkynylation–cyclization–iodination–alkylation sequence

Diaroyl‐S,N‐ketene Acetals: Red‐Shifted Solid‐State and Aggregation‐Induced Emitters from a One‐Pot Synthesis

Cyclohexene‐Embedded Dicyanomethylene Merocyanines – Consecutive Three‐Component Coupling‐Addition Synthesis and Chromophore Characteristics

Consecutive Four-Component Coupling-Addition Aza-Anellation Pictet–Spengler Synthesis of Tetrahydro-β-Carbolines: An Optimized Michael Addition and Computational Study on the Aza-Anellation Step

Bis[1]benzothieno[1,4]thiaborins as a Platform for BODIPY Singlet Oxygen Photosensitizers

Front Cover: Bis[1]benzothieno[1,4]thiaborins as a Platform for BODIPY Singlet Oxygen Photosensitizers (Chem. Eur. J. 36/2023)

Solid-state fluorescent 3,3-diarylallylidene indolinones by pseudo-five-component synthesis

Collaborators (9)

Christian Ganter

Krzysztof Wozniak

Jürgen Zeier

Krzysztof Durka

Agata Blacha-Grzechnik

Markus Suta

Sebastian Wesselborg

Klaus Meerholz

Karina Stephanie Krings

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