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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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Bidentate Lewis Base Adducts of Methyltrioxidorhenium(VII): Ligand Influence on Catalytic Performance and Stability

TL;DR: In this article, the 2,2'-bipyridine derived complexes exhibit good catalytic activities for cyclooctene epoxidation in a biphasic H(2)O(2)/organic solvent catalytic system using hydrogen peroxide as oxidizing agent.
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Synthesis and Structural Characterisation of an Isomorphous Series of Bis(imidazolin‐2‐imine) Metal Dichlorides Containing the First Row Transition Metals Mn, Fe, Co, Ni, Cu and Zn

TL;DR: The bis(imidazolin)-2-imine ligand N,N′-bis(1,3-diisopropyl-4,5-dimethylimidazalin-2-ylidene)-1,2-ethanediamine (BLiPr) was used to synthesize a complete series of transition metal dichloride complexes of the type [(BLiP)MCl2] with M = Mn, Fe, Co, Ni, Cu, Zn] as discussed by the authors.
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Synthesis and Catalytic Applications of ansa Compounds with Cycloalkyl Moieties as Bridging Units: A Comparative Study

TL;DR: In this paper, the molybdenum and tungsten compounds (Moeta(5)-C(5)H(5)[CH(CH(2))(n)]-eta(1)-CH(CO)(3)) and (Weta( 5]-C(4)-H(4)
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Hydrogen bond induced enantioselectivity in Mn(salen)-catalysed sulfoxidaton reactions

TL;DR: A chiral Mn(salen) complex exhibiting two lactam binding sites at two rigid 1,5,7-trimethyl-3-azabicyclo[3.3.1]nonan-2-one skeletons is capable of enantioselective sulfoxidation due to spatially remote substrate hydrogen bonding.
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Mechanistic Investigations of the Stereoselective Rare Earth Metal-Mediated Ring-Opening Polymerization of β-Butyrolactone

TL;DR: Experimental and computational results converge in one specific mechanism for the ring-opening polymerization of BL and even allow us to rationalize the preference for syndiotactic PHB.