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.
Papers
More filters
Journal ArticleDOI
Multifrequency ESR in ET2 MnCu[N(CN)(2)](4): A radical cation salt with quasi-two-dimensional magnetic layers in a three-dimensional polymeric structure
Kálmán L. Nagy,Bálint Náfrádi,Bálint Náfrádi,Nataliya D. Kushch,Eduard B. Yagubskii,Eberhardt Herdtweck,Titusz Fehér,L. F. Kiss,L. Forró,András Jánossy +9 more
TL;DR: In this paper, the radical cation salt, ET2MnCu[N(CN)(2)](4), [ET=bis(ethylenedithio)tetrathiafulvalene] with an unusual three-dimensional anionic polymeric network is studied by x-ray diffraction, static susceptibility measurements, and electron spin resonance (ESR) at frequencies between 9 and 420 GHz.
Journal ArticleDOI
Preparation of the enantiomers of an N-methylpyrrole analogue of Tröger's base
TL;DR: The enantiomers of bis(1-phenylethyl)-4,9-methano-1,6-dimethyl-4,5,9,10-tetrahydro-1H,6H-dipyrrolo-[3,2-b:3′,2′-f][1,5]diazocin-2,7-dicarboxylate were obtained by crystallization-induced asymmetric transformation.
Journal ArticleDOI
A photocycloaddition/fragmentation approach toward the 3,12-dioxatricyclo[8.2.1.0(6,13)]tridecane skeleton of terpenoid natural products.
TL;DR: Starting from tetronate 1 (R = CH(2)OH), a short photochemical access to the 3,12-dioxatricyclo[8.2.1.0(6,13)]tridecane-skeleton 2 of briarellin and asbestinin diterpenes has been explored and a two-step reaction pathway to the bicyclic ketolactone 3 was discovered.
Journal ArticleDOI
Complete Control of Regioselectivity in the Intramolecular [2 + 2] Photocycloaddition of 2-Alkenyl-3(2H)-furanones by the Length of the Side Chain
TL;DR: The 2-(omega-alkenyl)-substituted 2-methyl-3(2H)-furanones 2a and 2b were prepared from biacetyl (3) in four reaction steps and in overall yields of 20% and 21%, respectively, and the regioselectivity in the photocycloaddition was completely reversed.
Journal ArticleDOI
Synthesis and Neurotrophic Activity Studies of Illicium Sesquiterpene Natural Product Analogues
Johannes Richers,Alexander Pöthig,Eberhardt Herdtweck,Claudia Sippel,Felix Hausch,Konrad Tiefenbacher,Konrad Tiefenbacher +6 more
TL;DR: It is indicated that the promising biological activity can be retained by structurally simpler natural product analogues, which are accessible by a straightforward synthetic route.