Magnus Rueping

Prof. Magnus Rueping

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Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

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

Representative Publications

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4 December 2013 in Chemical Reviews
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CVChandra M. R. Volla
Chandra M. R. Volla
IAIuliana Atodiresei
Iuliana Atodiresei
Magnus RuepingMagnus Rueping
Magnus Rueping

18 May 2006 in Angewandte Chemie International Edition
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Magnus RuepingMagnus Rueping
Magnus Rueping
AAAndrey P. Antonchick
Andrey P. Antonchick
TTThomas Theissmann
Thomas Theissmann

20 January 2010 in Beilstein Journal of Organic Chemistry
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Magnus RuepingMagnus Rueping
Magnus Rueping
BNBoris J. Nachtsheim
Boris J. Nachtsheim
The development of efficient Friedel–Crafts alkylations of arenes and heteroarenes using only catalytic amounts of a Lewis acid has gained much attention over the last decade. The new catalytic approaches described in this review are favoured over classical Friedel–Crafts conditions as benzyl-, propargyl- and allyl alcohols, or styrenes, can be used instead of toxic benzyl halides. Additionally, only low catalyst loadings are needed to provide a wide range of products. Following a short introduction about the origin and classical definition of the Friedel–Crafts reaction, the review will describe the different environmentally benign substrates which can be applied today as an approach towards greener processes. Additionally, the first diastereoselective and enantioselective Friedel–Crafts-type alkylations will be highlighted.

25 May 2011 in Chemical Society Reviews
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Magnus RuepingMagnus Rueping
Magnus Rueping
AKAlexander Kuenkel
Alexander Kuenkel
IAIuliana Atodiresei
Iuliana Atodiresei
Chiral phosphoric acids and derivatives have attracted considerable attention as a powerful tool in asymmetric catalysis. Various enantioselective reactions have been developed by using these efficient Brønsted acid organocatalysts. Although initially the activation was restricted to reactive Brønsted basic substrates, recent reports are demonstrating the versatility of phosphoric acid catalysts in the activation of carbonyl compounds in a stereochemically controlled fashion. This tutorial review gives an overview of enantioselective Brønsted acid catalyzed transformations with the main focus on carbonyl activation. Different activation modes, key features of the catalysts and the applied substrates are presented and discussed with the goal to elucidate the origin of stereoselectivity in these Brønsted acid catalyzed transformations.

26 July 2005 in Organic Letters
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Magnus RuepingMagnus Rueping
Magnus Rueping
ESErli Sugiono
Erli Sugiono
CACengiz Azap
Cengiz Azap
TTThomas Theissmann
Thomas Theissmann
MBMichael Bolte
Michael Bolte