E
Eberhardt Herdtweck
Researcher at Technische Universität München
Publications - 332
Citations - 11434
Eberhardt Herdtweck is an academic researcher from Technische Universität München. The author has contributed to research in topics: Catalysis & Carbene. The author has an hindex of 56, co-authored 332 publications receiving 10785 citations. Previous affiliations of Eberhardt Herdtweck include Jordan University of Science and Technology & Ludwig Maximilian University of Munich.
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1-Aryl-3-(dimethylamino)propenones: Strong Proton Acceptors for Hydrogen Bonds
TL;DR: In this article, the electron-donating effects of 1-aryl-3-(dimethylamino)prop-2-en-1-ones are investigated by structural techniques (X-ray and neutron diffraction), spectroscopy, and density functional calculations.
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Oxovanadium(IV) complexes as molecular catalysts in epoxidation: Simple access to pyridylalkoxide derivatives
Gerhard M. Lobmaier,Harald Trauthwein,Guido D. Frey,Bernd Scharbert,Eberhardt Herdtweck,Wolfgang A. Herrmann +5 more
TL;DR: In this article, the metal-oxo complexes (1, 4, 6, 7, 8) demonstrated the ability to catalyse epoxidation reactions of alkenes with molecular oxygen and showed the expected square planar pyramidal geometry with the pyridine ring nitrogens in transposition to each other.
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Monocyclopentadienyl Chloro Bisphenoxo Ti(η5-C5H4SiMe2Cl)(η2-MBMP)Cl Derivative: Ti−Cl, Ti−O, and Si−Cl Reactivity. Crystal Structure of Ti(η5-C5H4SiMe3)(η2-MBMP)Cl and Ti(η5-C5H4SiMe2-η1-MBMP)(CH2Ph)2
TL;DR: The monocyclopentadienyl η2bisphenoxo chloro compound Ti(η5-C5H4SiMe3)(η2-MBMP)Cl (3) has been prepared in this paper.
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Reactivity of Yttrium Carboxylates Toward Alkylaluminum Hydrides
TL;DR: Yttrocene-carboxylate complex was synthesized as a spectroscopically versatile model system for investigating the reactivity of alkylaluminum hydrides towards rare-earth-metal carboxylates.
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Intramolecular Diels–Alder reactions with substituted Feringa-butenolides: a dramatic increase in reactivity by double activation
TL;DR: In this paper, a thermal intramolecular endo-selective Diels-Alder reaction with a substituted Feringa-butenolide was described and the structure of the main product was determined by single crystal X-ray analysis.