TY - JOUR A1 - Hetenyi, Gyorgy A1 - Molinari, Irene A1 - Clinton, John A1 - Bokelmann, Gotz A1 - Bondar, Istvan A1 - Crawford, Wayne C. A1 - Dessa, Jean-Xavier A1 - Doubre, Cecile A1 - Friederich, Wolfgang A1 - Fuchs, Florian A1 - Giardini, Domenico A1 - Graczer, Zoltan A1 - Handy, Mark R. A1 - Herak, Marijan A1 - Jia, Yan A1 - Kissling, Edi A1 - Kopp, Heidrun A1 - Korn, Michael A1 - Margheriti, Lucia A1 - Meier, Thomas A1 - Mucciarelli, Marco A1 - Paul, Anne A1 - Pesaresi, Damiano A1 - Piromallo, Claudia A1 - Plenefisch, Thomas A1 - Plomerova, Jaroslava A1 - Ritter, Joachim A1 - Rumpker, Georg A1 - Sipka, Vesna A1 - Spallarossa, Daniele A1 - Thomas, Christine A1 - Tilmann, Frederik A1 - Wassermann, Joachim A1 - Weber, Michael A1 - Weber, Zoltan A1 - Wesztergom, Viktor A1 - Zivcic, Mladen A1 - Abreu, Rafael A1 - Allegretti, Ivo A1 - Apoloner, Maria-Theresia A1 - Aubert, Coralie A1 - Besancon, Simon A1 - de Berc, Maxime Bes A1 - Brunel, Didier A1 - Capello, Marco A1 - Carman, Martina A1 - Cavaliere, Adriano A1 - Cheze, Jerome A1 - Chiarabba, Claudio A1 - Cougoulat, Glenn A1 - Cristiano, Luigia A1 - Czifra, Tibor A1 - Danesi, Stefania A1 - Daniel, Romuald A1 - Dannowski, Anke A1 - Dasovic, Iva A1 - Deschamps, Anne A1 - Egdorf, Sven A1 - Fiket, Tomislav A1 - Fischer, Kasper A1 - Funke, Sigward A1 - Govoni, Aladino A1 - Groschl, Gidera A1 - Heimers, Stefan A1 - Heit, Ben A1 - Herak, Davorka A1 - Huber, Johann A1 - Jaric, Dejan A1 - Jedlicka, Petr A1 - Jund, Helene A1 - Klingen, Stefan A1 - Klotz, Bernhard A1 - Kolinsky, Petr A1 - Kotek, Josef A1 - Kuhne, Lothar A1 - Kuk, Kreso A1 - Lange, Dietrich A1 - Loos, Jurgen A1 - Lovati, Sara A1 - Malengros, Deny A1 - Maron, Christophe A1 - Martin, Xavier A1 - Massa, Marco A1 - Mazzarini, Francesco A1 - Metral, Laurent A1 - Moretti, Milena A1 - Munzarova, Helena A1 - Nardi, Anna A1 - Pahor, Jurij A1 - Pequegnat, Catherine A1 - Petersen, Florian A1 - Piccinini, Davide A1 - Pondrelli, Silvia A1 - Prevolnik, Snjezan A1 - Racine, Roman A1 - Regnier, Marc A1 - Reiss, Miriam A1 - Salimbeni, Simone A1 - Santulin, Marco A1 - Scherer, Werner A1 - Schippkus, Sven A1 - Schulte-Kortnack, Detlef A1 - Solarino, Stefano A1 - Spieker, Kathrin A1 - Stipcevic, Josip A1 - Strollo, Angelo A1 - Sule, Balint A1 - Szanyi, Gyongyver A1 - Szucs, Eszter A1 - Thorwart, Martin A1 - Ueding, Stefan A1 - Vallocchia, Massimiliano A1 - Vecsey, Ludek A1 - Voigt, Rene A1 - Weidle, Christian A1 - Weyland, Gauthier A1 - Wiemer, Stefan A1 - Wolf, Felix A1 - Wolyniec, David A1 - Zieke, Thomas T1 - The AlpArray seismic network BT - a large-scale european experiment to image the alpine orogen JF - Surveys in Geophysics N2 - The AlpArray programme is a multinational, European consortium to advance our understanding of orogenesis and its relationship to mantle dynamics, plate reorganizations, surface processes and seismic hazard in the Alps-Apennines-Carpathians-Dinarides orogenic system. The AlpArray Seismic Network has been deployed with contributions from 36 institutions from 11 countries to map physical properties of the lithosphere and asthenosphere in 3D and thus to obtain new, high-resolution geophysical images of structures from the surface down to the base of the mantle transition zone. With over 600 broadband stations operated for 2 years, this seismic experiment is one of the largest simultaneously operated seismological networks in the academic domain, employing hexagonal coverage with station spacing at less than 52 km. This dense and regularly spaced experiment is made possible by the coordinated coeval deployment of temporary stations from numerous national pools, including ocean-bottom seismometers, which were funded by different national agencies. They combine with permanent networks, which also required the cooperation of many different operators. Together these stations ultimately fill coverage gaps. Following a short overview of previous large-scale seismological experiments in the Alpine region, we here present the goals, construction, deployment, characteristics and data management of the AlpArray Seismic Network, which will provide data that is expected to be unprecedented in quality to image the complex Alpine mountains at depth. KW - Seismology KW - Alps KW - Seismic network KW - Geodynamics KW - Seismic imaging KW - Mountain building Y1 - 2018 U6 - https://doi.org/10.1007/s10712-018-9472-4 SN - 0169-3298 SN - 1573-0956 VL - 39 IS - 5 SP - 1009 EP - 1033 PB - Springer CY - Dordrecht ER - TY - JOUR A1 - Schmidt, Bernd A1 - Wolf, Felix T1 - Synthesis of Phenylpropanoids via Matsuda-Heck Coupling of Arene Diazonium Salts JF - The journal of organic chemistry N2 - The Pd-catalyzed Heck-type coupling (Matsuda Heck reaction) of electron rich arene diazonium salts with electron deficient olefins has been exploited for the synthesis of phenylpropanoid natural products. Examples described herein are the naturally occurring benzofurans methyl wutaifuranate, wutaifuranol, wutaifuranal, their 7-methoxy derivatives, and the O-prenylated natural products boropinols A and C. Y1 - 2017 U6 - https://doi.org/10.1021/acs.joc.7b00447 SN - 0022-3263 VL - 82 SP - 4386 EP - 4395 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Schmidt, Bernd A1 - Wolf, Felix A1 - Brunner, Heiko T1 - Styrylsulfonates and -Sulfonamides through Pd-Catalysed Matsuda-Heck Reactions of Vinylsulfonic Acid Derivatives and Arenediazonium Salts JF - European journal of organic chemistry N2 - Arene diazonium salts undergo Matsuda-Heck reactions with vinylsulfonates and -sulfonamides to give styrylsulfonic acid derivatives in high to excellent yields and with high to excellent selectivities. By quantifying the evolution of nitrogen over time in a gas-meter apparatus, the reactivities of ethylvinylsulfonate and the benchmark olefin methyl acrylate were compared for an electron-rich and an -deficient arene diazonium salt. Tertiary sulfonamides react in Matsuda-Heck couplings with high conversions, but require long reaction times, which prevents the determination of kinetic data through the measurement of nitrogen evolution. Secondary sulfonamides were found to be unreactive. From these results, the following order of reactivity could be deduced: H2C=CHCO2Me > H2C=CHSO2OEt > H2C=CHSO2N(Me)Bn >> H2C=CHSO2NHBn. Through the Matsuda-Heck coupling of 5-indolyldiazonium salt and a tertiary vinylsulfonamide, the synthesis of the C-5-substituted indole part of the antimigraine drug naratriptan was accomplished in high yield. KW - Homogeneous catalysis KW - Cross-coupling KW - Palladium KW - Sulfonamides KW - Alkenes KW - Drug design Y1 - 2016 U6 - https://doi.org/10.1002/ejoc.201600469 SN - 1434-193X SN - 1099-0690 SP - 2972 EP - 2982 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Schmidt, Bernd A1 - Wolf, Felix A1 - Ehlert, Christopher T1 - Systematic Investigation into the Matsuda-Heck Reaction of alpha-Methylene Lactones: How Conformational Constraints Direct the beta-H-Elimination Step JF - The journal of organic chemistry N2 - alpha-Methylene-gamma-butyrolactone and alpha-methylene-gamma-valerolactone undergo Pd-catalyzed Matsuda-Heck couplings with arene diazonium salts to alpha-benzyl butenolides or pentenolides, respectively, or to alpha-benzylidene lactones. The observed regioselectivity is strongly ring size dependent, with six-membered rings giving exclusively alpha-benzyl pentenolides, whereas the five-membered alpha-methylene lactone reacts to mixtures of regioisomers with a high proportion of (E)-alpha-benzylidene-gamma-butyrolactones. DFT calculations suggest that the reasons for these differences are not thermodynamic but kinetic in nature. The relative energies of the conformers of the Pd sigma-complexes resulting from insertion into the Pd-aryl bond were correlated with the dihedral angles between Pd and endo-beta-H. This correlation revealed that in the case of the six-membered lactone an energetically favorable conformer adopts a nearly synperiplanar Pd/endo-beta-H arrangement, whereas for the analogous Pd sigma-complex of the five-membered lactone the smallest Pd/endo-beta-H dihedral angle is observed for a conformer with a comparatively high potential energy. The optimized conditions for Matsuda-Heck arylations of exo-methylene lactones were eventually applied to the synthesis of the natural product anemarcoumarin A. Y1 - 2016 U6 - https://doi.org/10.1021/acs.joc.6b02207 SN - 0022-3263 VL - 81 SP - 11235 EP - 11249 PB - American Chemical Society CY - Washington ER - TY - THES A1 - Wolf, Felix T1 - Neuartige Olefine und Aryldiazoniumtetrafluoroborate für die MATSUDA-HECK-Reaktion Y1 - 2016 ER -