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
A Convenient Synthesis of Benzonitriles via Electrophilic Cyanation with N‐Cyanobenzimidazole.
TL;DR: In situ generated aryl and hetero-aryl Grignard compounds are cyanated by nitrile (II) to give benzonitriles as discussed by the authors, which is used to synthesize benzonitrile.
A Base-Catalyzed Domino-Isomerization—Hydroamination Reaction — A New Synthetic Route to Amphetamines.
TL;DR: In this paper, an efficient synthesis of pharmaceutically interesting amphetamines by a base-catalyzed domino-isomerization-hydroamination reaction is presented.
Patent
Process for the preparation of aromatic acetyles using palladacyclen as acatalysts
Matthias Beller,Wolfgang A. Herrmann,C.‐P. Reisinger +2 more
- 22 Apr 1996
TL;DR: In this paper, the prodn. of an aromatic acetylene of formula Ar-C IDENTICAL C-R8a (I) comprises reacting an halo-aromatic or aryl-sulphonate of formula AR-X (II) with an acetylene in presence of a Pd cpd. of formula (IV) as catalyst.
Base‐Catalyzed Synthesis of N‐(2‐Arylethyl)anilines and Base‐Promoted Domino Synthesis of 2,3‐Dihydroindoles.
TL;DR: In this article, the use of potassium tert-butyl alcoholate enables the selective addition of primary anilines to substituted styrenes and a new domino reaction, consisting of a hydroamination and an aryne cyclization.
Gold‐Catalyzed Benzylation of Arenes and Heteroarenes.
TL;DR: Friedel-Crafts type benzylation of arenes and heteroarenes with benzylic acetates, alcohols, and carbonates is effectively promoted under mild reaction conditions using catalytic amounts of gold salts as discussed by the authors.