Matthias Beller
University of Rostock
803 Papers
7.1K Citations
Matthias Beller is an academic researcher from University of Rostock. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 113, co-authored 733 publications. Previous affiliations of Matthias Beller include Technische Universität München & Ludwig Maximilian University of Munich.
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Papers
The Development of a Lead-Free Replacement for the Lindlar Catalyst for Alkyne Semi-Hydrogenation Using Silica Supported, N-doped Carbon Modified Cobalt Nanoparticles
Peter McNeice,Marc-André Müller,Jonathan Medlock,Werner Bonrath,Nils Rockstroh,Stephan Bartling,Henrik Lund,Kathrin Junge,Matthias Beller +8 more
TL;DR: In this paper , the synthesis of vitamin precursors via alkyne semi-hydrogenation has been achieved with a lead and palladium-free catalyst, which was used to modify Cobalt nanoparticles modified by nitrogen doped carbon and supported on silica.
Ruthenium‐Catalyzed Alkoxycarbonylation of Alkenes with Paraformaldehyde as a Carbon Monoxide Substitute
TL;DR: In this article, the first efficient use of paraformaldehyde in the alkoxy carbonylation of alkenes is reported, using a combination of readily available [Ru3(CO)12] and PCy3 (Cy=cyclohexyl) as catalyst, industrially important esters are produced in good to high yield (up to 90%) at relatively low temperature.
Hypervalent-iodine Promoted Selective Cleavage of C(sp3)-C(sp3) Bonds in Ethers
TL;DR: In this paper , a visible light-promoted and radical-mediated strategy for the site-specific cleavage of C(sp3)-C(sp 3) bonds in ethers is reported.
Synthesis of 3-(2-N,N-diethylaminoethoxy)indoles as potential 5-HT6 receptor ligands
Karolin Alex,Nicolle Schwarz,Vivek Khedkar,Iliyas Ali Sayyed,Annegret Tillack,Dirk Michalik,Joerg Holenz,Jose Luis Diaz,Matthias Beller +8 more
TL;DR: The synthesis of new pharmaceutically interesting 3-(2-N,N-diethylaminoethoxy)indole derivatives is described, and sulfonylation of these novel indoles gave access to potential 5-HT(6) receptor ligands.