Matthias Beller

Matthias Beller

orcid

Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 December 2009 in Advanced Synthesis & Catalysis
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Journal Article
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CTChristian Torborg
Christian Torborg
MBMatthias Beller
Matthias Beller

19 May 2009 in Angewandte Chemie International Edition
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Journal Article
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ABAnne Brennführer
Anne Brennführer
HNHelfried Neumann
Helfried Neumann
MBMatthias Beller
Matthias Beller

15 April 2008 in Angewandte Chemie International Edition
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Journal Article
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SEStephan Enthaler
Stephan Enthaler
KJKathrin Junge
Kathrin Junge
MBMatthias Beller
Matthias Beller

12 June 2018 in Nature Catalysis
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Journal Article
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XCXinjiang Cui
Xinjiang Cui
WLWu Li
Wu Li
PRPavel Ryabchuk
Pavel Ryabchuk
KJKathrin Junge
Kathrin Junge
MBMatthias Beller
Matthias Beller

6 October 2017 in Chemical Reviews
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Journal Article
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KSKaterina Sordakis
Katerina Sordakis
Conghui TangConghui Tang
Conghui Tang
LVLydia K. Vogt
Lydia K. Vogt
HJHenrik Junge
Henrik Junge
PDPaul Dyson
Paul Dyson
GLGabor Laurenczy
Gabor Laurenczy

29 November 2013 in Science
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Jagadeesh RajenahallyJagadeesh Rajenahally
Jagadeesh Rajenahally
ASAnnette-Enrica Surkus
Annette-Enrica Surkus
HJHenrik Junge
Henrik Junge
MPMarga-Martina Pohl
Marga-Martina Pohl
JRJorg Radnik
Jorg Radnik
MBMatthias Beller
Matthias Beller
Lighter Hydrogenation Catalysts: Enzymes have evolved to use abundant metals such as iron, cobalt, and nickel for redox catalysis. However, synthetic catalysis has generally relied on the rarer, heavier relatives of these elements: ruthenium, rhodium, iridium, palladium, and platinum (see the Perspective by Bullock ). Friedfeld et al. (p. 1076 ) used high-throughput screening to show that the right cobalt precursor can be activated for asymmetric hydrogenation catalysis by using the traditional ligands developed for the precious metals. Zuo et al. (p. 1080 ) focused on iron, demonstrating a highly effective asymmetric transfer hydrogenation catalyst that uses a ligand rationally designed after careful mechanistic study. Jagadeesh et al. (p. 1073 ) prepared supported iron catalysts that selectively reduce nitro substituents on aromatic rings to amines, thereby facilitating the preparation of a wide range of aniline derivatives.