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{{Notability|date=January 2023}}
{{COI|date=January 2023}}
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Peters studied chemistry at [[RWTH Aachen University]] from 1992 to 1997 and subsequently received his doctorate under [[Dieter Enders]] until 2000. This was followed by a stay as a postdoc at [[Harvard University]] with [[Yoshito Kishi]] as a [[DAAD scholarship]] holder. Between 2001 and 2004 he worked as a process research chemist at [[Roche|F. Hoffmann-La Roche LTD]] (Basel). From 2004 to 2008, Peters was an assistant professor at [[ETH Zurich]]. Since 2008 he has been Professor of Organic Chemistry at the University of Stuttgart.
Peters studied chemistry at [[RWTH Aachen University]] from 1992 to 1997 and subsequently received his doctorate under [[Dieter Enders]] until 2000. This was followed by a stay as a postdoc at [[Harvard University]] with [[Yoshito Kishi]] as a [[DAAD scholarship]] holder. Between 2001 and 2004 he worked as a process research chemist at [[Roche|F. Hoffmann-La Roche LTD]] (Basel). From 2004 to 2008, Peters was an assistant professor at [[ETH Zurich]]. Since 2008 he has been Professor of Organic Chemistry at the University of Stuttgart.


The research team led by Prof. Peters contributes to the field of cooperative [[asymmetric catalysis]].<ref>{{Cite book |last=Peters |first=René |title=Cooperative Catalysis – Designing Efficient Catalysts for Synthesis |year=2015 |location=Weinheim}}</ref> The research is focused around the development of bi- and polyfunctional catalysts whose mode of action is inspired by [[Enzyme|enzymes]], although the structure of the artificial catalysts is much simpler than those of enzymes. In the Peters catalysts, a [[Lewis acids and bases|Lewis acid]] often cooperates with charged, non-metallic functionalities such as [[ammonium]],<ref>{{Cite journal |last=Brodbeck |first=Daniel |last2=Broghammer |first2=Florian |last3=Meisner |first3=Jan |last4=Klepp |first4=Julian |last5=Garnier |first5=Delphine |last6=Frey |first6=Wolfgang |last7=Kästner |first7=Johannes |last8=Peters |first8=René |date=2017-03-27 |title=An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201612493 |journal=Angewandte Chemie International Edition |language=en |volume=56 |issue=14 |pages=4056–4060 |doi=10.1002/anie.201612493}}</ref><ref>{{Cite journal |last=Titze |first=Marvin |last2=Heitkämper |first2=Juliane |last3=Junge |first3=Thorsten |last4=Kästner |first4=Johannes |last5=Peters |first5=René |date=2021-03-01 |title=Highly Active Cooperative Lewis Acid—Ammonium Salt Catalyst for the Enantioselective Hydroboration of Ketones |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202012796 |journal=Angewandte Chemie International Edition |language=en |volume=60 |issue=10 |pages=5544–5553 |doi=10.1002/anie.202012796 |issn=1433-7851 |pmc=PMC7986937 |pmid=33210781}}</ref> [[pyridinium]]<ref>{{Cite journal |last=Kull |first=Thomas |last2=Peters |first2=René |date=2008-07-07 |title=Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis of trans ‐Configured β‐Lactones |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200801143 |journal=Angewandte Chemie International Edition |language=en |volume=47 |issue=29 |pages=5461–5464 |doi=10.1002/anie.200801143}}</ref> or olium salts,<ref>{{Cite journal |last=Mechler |first=Melanie |last2=Peters |first2=René |date=2015-08-24 |title=Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201502930 |journal=Angewandte Chemie International Edition |language=en |volume=54 |issue=35 |pages=10303–10307 |doi=10.1002/anie.201502930}}</ref><ref>{{Cite journal |last=Schmid |first=Juliane |last2=Junge |first2=Thorsten |last3=Lang |first3=Johannes |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2019-04-08 |title=Polyfunctional Bis‐Lewis‐Acid‐/Bis‐Triazolium Catalysts for Stereoselective 1,4‐Additions of 2‐Oxindoles to Maleimides |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201814453 |journal=Angewandte Chemie International Edition |language=en |volume=58 |issue=16 |pages=5447–5451 |doi=10.1002/anie.201814453 |issn=1433-7851}}</ref> betaine units<ref>{{Cite journal |last=Willig |first=Felix |last2=Lang |first2=Johannes |last3=Hans |first3=Andreas C. |last4=Ringenberg |first4=Mark R. |last5=Pfeffer |first5=Daniel |last6=Frey |first6=Wolfgang |last7=Peters |first7=René |date=2019-07-31 |title=Polyfunctional Imidazolium Aryloxide Betaine/Lewis Acid Catalysts as Tools for the Asymmetric Synthesis of Disfavored Diastereomers |url=https://pubs.acs.org/doi/10.1021/jacs.9b04902 |journal=Journal of the American Chemical Society |language=en |volume=141 |issue=30 |pages=12029–12043 |doi=10.1021/jacs.9b04902 |issn=0002-7863}}</ref><ref>{{Cite journal |last=Miskov‐Pajic |first=Vukoslava |last2=Willig |first2=Felix |last3=Wanner |first3=Daniel M. |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2020-11-02 |title=Enantiodivergent [4+2] Cycloaddition of Dienolates by Polyfunctional Lewis Acid/Zwitterion Catalysis |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202009093 |journal=Angewandte Chemie International Edition |language=en |volume=59 |issue=45 |pages=19873–19877 |doi=10.1002/anie.202009093 |issn=1433-7851 |pmc=PMC7693193 |pmid=32697020}}</ref> and classical hydrogen bond donors.<ref>{{Cite journal |last=Mechler |first=Melanie |last2=Peters |first2=René |date=2015-08-24 |title=Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201502930 |journal=Angewandte Chemie International Edition |language=en |volume=54 |issue=35 |pages=10303–10307 |doi=10.1002/anie.201502930}}</ref><ref>{{Cite journal |last=Schmid |first=Juliane |last2=Junge |first2=Thorsten |last3=Lang |first3=Johannes |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2019-04-08 |title=Polyfunctional Bis‐Lewis‐Acid‐/Bis‐Triazolium Catalysts for Stereoselective 1,4‐Additions of 2‐Oxindoles to Maleimides |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201814453 |journal=Angewandte Chemie International Edition |language=en |volume=58 |issue=16 |pages=5447–5451 |doi=10.1002/anie.201814453 |issn=1433-7851}}</ref> Through the different catalyst functional groups, simultaneous activation and a precise spatial alignment of both reactants is often possible, so that high catalytic activity can be combined with very high stereocontrol. In addition to the development of catalysts for asymmetric catalysis, the Peters research group investigates their mechanistic mode of action in an interdisciplinary approach.
The research team led by Prof. Peters contributes to the field of cooperative [[asymmetric catalysis]].<ref>{{Cite book |last=Peters |first=René |title=Cooperative Catalysis – Designing Efficient Catalysts for Synthesis |year=2015 |location=Weinheim}}</ref> The research is focused around the development of bi- and polyfunctional catalysts whose mode of action is inspired by [[Enzyme|enzymes]], although the structure of the artificial catalysts is much simpler than those of enzymes. In the Peters catalysts, a [[Lewis acids and bases|Lewis acid]] often cooperates with charged, non-metallic functionalities such as [[ammonium]],<ref>{{Cite journal |last=Brodbeck |first=Daniel |last2=Broghammer |first2=Florian |last3=Meisner |first3=Jan |last4=Klepp |first4=Julian |last5=Garnier |first5=Delphine |last6=Frey |first6=Wolfgang |last7=Kästner |first7=Johannes |last8=Peters |first8=René |date=2017-03-27 |title=An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201612493 |journal=Angewandte Chemie International Edition |language=en |volume=56 |issue=14 |pages=4056–4060 |doi=10.1002/anie.201612493}}</ref><ref>{{Cite journal |last=Titze |first=Marvin |last2=Heitkämper |first2=Juliane |last3=Junge |first3=Thorsten |last4=Kästner |first4=Johannes |last5=Peters |first5=René |date=2021-03-01 |title=Highly Active Cooperative Lewis Acid—Ammonium Salt Catalyst for the Enantioselective Hydroboration of Ketones |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202012796 |journal=Angewandte Chemie International Edition |language=en |volume=60 |issue=10 |pages=5544–5553 |doi=10.1002/anie.202012796 |issn=1433-7851 |pmc=PMC7986937 |pmid=33210781}}</ref> [[pyridinium]]<ref name=":0">{{Cite journal |last=Kull |first=Thomas |last2=Peters |first2=René |date=2008-07-07 |title=Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis of trans ‐Configured β‐Lactones |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200801143 |journal=Angewandte Chemie International Edition |language=en |volume=47 |issue=29 |pages=5461–5464 |doi=10.1002/anie.200801143}}</ref> or olium salts,<ref>{{Cite journal |last=Mechler |first=Melanie |last2=Peters |first2=René |date=2015-08-24 |title=Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201502930 |journal=Angewandte Chemie International Edition |language=en |volume=54 |issue=35 |pages=10303–10307 |doi=10.1002/anie.201502930}}</ref><ref>{{Cite journal |last=Schmid |first=Juliane |last2=Junge |first2=Thorsten |last3=Lang |first3=Johannes |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2019-04-08 |title=Polyfunctional Bis‐Lewis‐Acid‐/Bis‐Triazolium Catalysts for Stereoselective 1,4‐Additions of 2‐Oxindoles to Maleimides |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201814453 |journal=Angewandte Chemie International Edition |language=en |volume=58 |issue=16 |pages=5447–5451 |doi=10.1002/anie.201814453 |issn=1433-7851}}</ref> [[betaine]] units<ref>{{Cite journal |last=Willig |first=Felix |last2=Lang |first2=Johannes |last3=Hans |first3=Andreas C. |last4=Ringenberg |first4=Mark R. |last5=Pfeffer |first5=Daniel |last6=Frey |first6=Wolfgang |last7=Peters |first7=René |date=2019-07-31 |title=Polyfunctional Imidazolium Aryloxide Betaine/Lewis Acid Catalysts as Tools for the Asymmetric Synthesis of Disfavored Diastereomers |url=https://pubs.acs.org/doi/10.1021/jacs.9b04902 |journal=Journal of the American Chemical Society |language=en |volume=141 |issue=30 |pages=12029–12043 |doi=10.1021/jacs.9b04902 |issn=0002-7863}}</ref><ref>{{Cite journal |last=Miskov‐Pajic |first=Vukoslava |last2=Willig |first2=Felix |last3=Wanner |first3=Daniel M. |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2020-11-02 |title=Enantiodivergent [4+2] Cycloaddition of Dienolates by Polyfunctional Lewis Acid/Zwitterion Catalysis |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202009093 |journal=Angewandte Chemie International Edition |language=en |volume=59 |issue=45 |pages=19873–19877 |doi=10.1002/anie.202009093 |issn=1433-7851 |pmc=PMC7693193 |pmid=32697020}}</ref> and classical [[hydrogen bond]] donors.<ref>{{Cite journal |last=Mechler |first=Melanie |last2=Peters |first2=René |date=2015-08-24 |title=Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201502930 |journal=Angewandte Chemie International Edition |language=en |volume=54 |issue=35 |pages=10303–10307 |doi=10.1002/anie.201502930}}</ref><ref>{{Cite journal |last=Schmid |first=Juliane |last2=Junge |first2=Thorsten |last3=Lang |first3=Johannes |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2019-04-08 |title=Polyfunctional Bis‐Lewis‐Acid‐/Bis‐Triazolium Catalysts for Stereoselective 1,4‐Additions of 2‐Oxindoles to Maleimides |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201814453 |journal=Angewandte Chemie International Edition |language=en |volume=58 |issue=16 |pages=5447–5451 |doi=10.1002/anie.201814453 |issn=1433-7851}}</ref> Through the different catalyst functional groups, simultaneous activation and a precise spatial alignment of both reactants is often possible, so that high catalytic activity can be combined with very high stereocontrol. In addition to the development of catalysts for asymmetric [[catalysis]], the Peters research group investigates their mechanistic mode of action in an interdisciplinary approach<ref name=":0" />.


The research group is also known for its development of planar chiral metallacycles,<ref>{{Cite journal |last=Weiss |first=Matthias E. |last2=Fischer |first2=Daniel F. |last3=Xin |first3=Zhuo-qun |last4=Jautze |first4=Sascha |last5=Schweizer |first5=W. Bernd |last6=Peters |first6=René |date=2006-08-25 |title=Practical, Highly Active, and Enantioselective Ferrocenyl–Imidazoline Palladacycle Catalysts (FIPs) for the Aza-Claisen Rearrangement ofN-para-Methoxyphenyl Trifluoroacetimidates |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200601731 |journal=Angewandte Chemie International Edition |language=en |volume=45 |issue=34 |pages=5694–5698 |doi=10.1002/anie.200601731 |issn=1433-7851}}</ref><ref>{{Cite journal |last=Huang |first=Haoxi |last2=Peters |first2=René |date=2009-01-05 |title=A Highly Strained Planar-Chiral Platinacycle for Catalytic Activation of Internal Olefins in the Friedel-Crafts Alkylation of Indoles |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200804944 |journal=Angewandte Chemie International Edition |language=en |volume=48 |issue=3 |pages=604–606 |doi=10.1002/anie.200804944}}</ref><ref>{{Cite journal |last=Fischer |first=Daniel F. |last2=Barakat |first2=Assem |last3=Xin |first3=Zhuo-qun |last4=Weiss |first4=Matthias E. |last5=Peters |first5=René |date=2009-09-07 |title=The Asymmetric Aza-Claisen Rearrangement: Development of Widely Applicable Pentaphenylferrocenyl Palladacycle Catalysts |url=https://onlinelibrary.wiley.com/doi/10.1002/chem.200900712 |journal=Chemistry - A European Journal |language=en |volume=15 |issue=35 |pages=8722–8741 |doi=10.1002/chem.200900712}}</ref><ref>{{Cite journal |last=Schrapel |first=Carmen |last2=Peters |first2=René |date=2015-08-24 |title=Exogenous-Base-Free Palladacycle-Catalyzed Highly Enantioselective Arylation of Imines with Arylboroxines |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201501846 |journal=Angewandte Chemie International Edition |language=en |volume=54 |issue=35 |pages=10289–10293 |doi=10.1002/anie.201501846}}</ref><ref>{{Cite journal |last=Pfeffer |first=Camilla |last2=Probst |first2=Patrick |last3=Wannenmacher |first3=Nick |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2022-08-26 |title=Direct Enantioselective Addition of Alkynes to Imines by a Highly Efficient Palladacycle Catalyst |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202206835 |journal=Angewandte Chemie International Edition |language=en |volume=61 |issue=35 |doi=10.1002/anie.202206835 |issn=1433-7851 |pmc=PMC9545068 |pmid=35701311}}</ref><ref>{{Cite journal |last=Yu |first=Xin |last2=Hu |first2=Lingfei |last3=Frey |first3=Wolfgang |last4=Lu |first4=Gang |last5=Peters |first5=René |date=2022-10-17 |title=Stereoretentive Regio‐ and Enantioselective Allylation of Isoxazolinones by a Planar Chiral Palladacycle Catalyst |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202210145 |journal=Angewandte Chemie International Edition |language=en |volume=61 |issue=42 |doi=10.1002/anie.202210145 |issn=1433-7851}}</ref> in which an intramolecular cooperation of two metal centers could often be used.<ref>{{Cite journal |last=Jautze |first=Sascha |last2=Peters |first2=René |date=2008-11-17 |title=Enantioselective Bimetallic Catalysis of Michael Additions Forming Quaternary Stereocenters |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200803539 |journal=Angewandte Chemie International Edition |language=en |volume=47 |issue=48 |pages=9284–9288 |doi=10.1002/anie.200803539 |issn=1433-7851}}</ref><ref>{{Cite journal |last=Weber |first=Manuel |last2=Jautze |first2=Sascha |last3=Frey |first3=Wolfgang |last4=Peters |first4=René |date=2010-09-08 |title=Bispalladacycle-Catalyzed Brønsted Acid/Base-Promoted Asymmetric Tandem Azlactone Formation−Michael Addition |url=https://pubs.acs.org/doi/10.1021/ja106088v |journal=Journal of the American Chemical Society |language=en |volume=132 |issue=35 |pages=12222–12225 |doi=10.1021/ja106088v |issn=0002-7863}}</ref><ref>{{Cite journal |last=Eitel |first=Simon H. |last2=Jautze |first2=Sascha |last3=Frey |first3=Wolfgang |last4=Peters |first4=René |date=2013 |title=Asymmetric Michael additions of α-cyanoacetates by soft Lewis acid/hard Brønsted acid catalysis: stereodivergency with bi- vs. monometallic catalysts |url=http://xlink.rsc.org/?DOI=c3sc50419k |journal=Chemical Science |language=en |volume=4 |issue=5 |pages=2218 |doi=10.1039/c3sc50419k |issn=2041-6520}}</ref>
The research group is also known for its development of planar chiral [[metallacycle]]<nowiki/>s,<ref>{{Cite journal |last=Weiss |first=Matthias E. |last2=Fischer |first2=Daniel F. |last3=Xin |first3=Zhuo-qun |last4=Jautze |first4=Sascha |last5=Schweizer |first5=W. Bernd |last6=Peters |first6=René |date=2006-08-25 |title=Practical, Highly Active, and Enantioselective Ferrocenyl–Imidazoline Palladacycle Catalysts (FIPs) for the Aza-Claisen Rearrangement ofN-para-Methoxyphenyl Trifluoroacetimidates |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200601731 |journal=Angewandte Chemie International Edition |language=en |volume=45 |issue=34 |pages=5694–5698 |doi=10.1002/anie.200601731 |issn=1433-7851}}</ref><ref>{{Cite journal |last=Huang |first=Haoxi |last2=Peters |first2=René |date=2009-01-05 |title=A Highly Strained Planar-Chiral Platinacycle for Catalytic Activation of Internal Olefins in the Friedel-Crafts Alkylation of Indoles |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200804944 |journal=Angewandte Chemie International Edition |language=en |volume=48 |issue=3 |pages=604–606 |doi=10.1002/anie.200804944}}</ref><ref>{{Cite journal |last=Fischer |first=Daniel F. |last2=Barakat |first2=Assem |last3=Xin |first3=Zhuo-qun |last4=Weiss |first4=Matthias E. |last5=Peters |first5=René |date=2009-09-07 |title=The Asymmetric Aza-Claisen Rearrangement: Development of Widely Applicable Pentaphenylferrocenyl Palladacycle Catalysts |url=https://onlinelibrary.wiley.com/doi/10.1002/chem.200900712 |journal=Chemistry - A European Journal |language=en |volume=15 |issue=35 |pages=8722–8741 |doi=10.1002/chem.200900712}}</ref><ref>{{Cite journal |last=Schrapel |first=Carmen |last2=Peters |first2=René |date=2015-08-24 |title=Exogenous-Base-Free Palladacycle-Catalyzed Highly Enantioselective Arylation of Imines with Arylboroxines |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.201501846 |journal=Angewandte Chemie International Edition |language=en |volume=54 |issue=35 |pages=10289–10293 |doi=10.1002/anie.201501846}}</ref><ref>{{Cite journal |last=Pfeffer |first=Camilla |last2=Probst |first2=Patrick |last3=Wannenmacher |first3=Nick |last4=Frey |first4=Wolfgang |last5=Peters |first5=René |date=2022-08-26 |title=Direct Enantioselective Addition of Alkynes to Imines by a Highly Efficient Palladacycle Catalyst |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202206835 |journal=Angewandte Chemie International Edition |language=en |volume=61 |issue=35 |doi=10.1002/anie.202206835 |issn=1433-7851 |pmc=PMC9545068 |pmid=35701311}}</ref><ref>{{Cite journal |last=Yu |first=Xin |last2=Hu |first2=Lingfei |last3=Frey |first3=Wolfgang |last4=Lu |first4=Gang |last5=Peters |first5=René |date=2022-10-17 |title=Stereoretentive Regio‐ and Enantioselective Allylation of Isoxazolinones by a Planar Chiral Palladacycle Catalyst |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.202210145 |journal=Angewandte Chemie International Edition |language=en |volume=61 |issue=42 |doi=10.1002/anie.202210145 |issn=1433-7851}}</ref> in which an intramolecular cooperation of two metal centers could often be used.<ref>{{Cite journal |last=Jautze |first=Sascha |last2=Peters |first2=René |date=2008-11-17 |title=Enantioselective Bimetallic Catalysis of Michael Additions Forming Quaternary Stereocenters |url=https://onlinelibrary.wiley.com/doi/10.1002/anie.200803539 |journal=Angewandte Chemie International Edition |language=en |volume=47 |issue=48 |pages=9284–9288 |doi=10.1002/anie.200803539 |issn=1433-7851}}</ref><ref>{{Cite journal |last=Weber |first=Manuel |last2=Jautze |first2=Sascha |last3=Frey |first3=Wolfgang |last4=Peters |first4=René |date=2010-09-08 |title=Bispalladacycle-Catalyzed Brønsted Acid/Base-Promoted Asymmetric Tandem Azlactone Formation−Michael Addition |url=https://pubs.acs.org/doi/10.1021/ja106088v |journal=Journal of the American Chemical Society |language=en |volume=132 |issue=35 |pages=12222–12225 |doi=10.1021/ja106088v |issn=0002-7863}}</ref><ref>{{Cite journal |last=Eitel |first=Simon H. |last2=Jautze |first2=Sascha |last3=Frey |first3=Wolfgang |last4=Peters |first4=René |date=2013 |title=Asymmetric Michael additions of α-cyanoacetates by soft Lewis acid/hard Brønsted acid catalysis: stereodivergency with bi- vs. monometallic catalysts |url=http://xlink.rsc.org/?DOI=c3sc50419k |journal=Chemical Science |language=en |volume=4 |issue=5 |pages=2218 |doi=10.1039/c3sc50419k |issn=2041-6520}}</ref>




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* [https://orcid.org/0000-0002-6668-4017 René Peters] - ORCID
* [https://orcid.org/0000-0002-6668-4017 René Peters] - ORCID
* [https://scholar.google.de/citations?user=GCh01V8AAAAJ&hl=de&oi=ao René Peters] - Google Scholar
* [https://scholar.google.de/citations?user=GCh01V8AAAAJ&hl=de&oi=ao René Peters] - Google Scholar
* Web of Science researcher ID: I-9702-2019<br />
* Web of Science researcher ID: I-9702-2019
* [https://www.researchgate.net/profile/Rene-Peters René Peters] - researchgate
* [https://everipedia.org/wiki/lang_en/rene-peters René Peters] - IQ.wiki
* [https://research.com/u/rene-peters René Peters] - research.com
* René [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201311144 Peters] - Wiley online library<br />


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Revision as of 17:12, 4 January 2023

René Peters (born August 26, 1971 in Simmerath) is a German chemist and since 2008 Professor of Organic Chemistry at the University of Stuttgart.

Life and work

Peters studied chemistry at RWTH Aachen University from 1992 to 1997 and subsequently received his doctorate under Dieter Enders until 2000. This was followed by a stay as a postdoc at Harvard University with Yoshito Kishi as a DAAD scholarship holder. Between 2001 and 2004 he worked as a process research chemist at F. Hoffmann-La Roche LTD (Basel). From 2004 to 2008, Peters was an assistant professor at ETH Zurich. Since 2008 he has been Professor of Organic Chemistry at the University of Stuttgart.

The research team led by Prof. Peters contributes to the field of cooperative asymmetric catalysis.[1] The research is focused around the development of bi- and polyfunctional catalysts whose mode of action is inspired by enzymes, although the structure of the artificial catalysts is much simpler than those of enzymes. In the Peters catalysts, a Lewis acid often cooperates with charged, non-metallic functionalities such as ammonium,[2][3] pyridinium[4] or olium salts,[5][6] betaine units[7][8] and classical hydrogen bond donors.[9][10] Through the different catalyst functional groups, simultaneous activation and a precise spatial alignment of both reactants is often possible, so that high catalytic activity can be combined with very high stereocontrol. In addition to the development of catalysts for asymmetric catalysis, the Peters research group investigates their mechanistic mode of action in an interdisciplinary approach[4].

The research group is also known for its development of planar chiral metallacycles,[11][12][13][14][15][16] in which an intramolecular cooperation of two metal centers could often be used.[17][18][19]


Further Information

References

  1. ^ Peters, René (2015). Cooperative Catalysis – Designing Efficient Catalysts for Synthesis. Weinheim.{{cite book}}: CS1 maint: location missing publisher (link)
  2. ^ Brodbeck, Daniel; Broghammer, Florian; Meisner, Jan; Klepp, Julian; Garnier, Delphine; Frey, Wolfgang; Kästner, Johannes; Peters, René (2017-03-27). "An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes". Angewandte Chemie International Edition. 56 (14): 4056–4060. doi:10.1002/anie.201612493.
  3. ^ Titze, Marvin; Heitkämper, Juliane; Junge, Thorsten; Kästner, Johannes; Peters, René (2021-03-01). "Highly Active Cooperative Lewis Acid—Ammonium Salt Catalyst for the Enantioselective Hydroboration of Ketones". Angewandte Chemie International Edition. 60 (10): 5544–5553. doi:10.1002/anie.202012796. ISSN 1433-7851. PMC 7986937. PMID 33210781.{{cite journal}}: CS1 maint: PMC format (link)
  4. ^ a b Kull, Thomas; Peters, René (2008-07-07). "Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis of trans ‐Configured β‐Lactones". Angewandte Chemie International Edition. 47 (29): 5461–5464. doi:10.1002/anie.200801143.
  5. ^ Mechler, Melanie; Peters, René (2015-08-24). "Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts". Angewandte Chemie International Edition. 54 (35): 10303–10307. doi:10.1002/anie.201502930.
  6. ^ Schmid, Juliane; Junge, Thorsten; Lang, Johannes; Frey, Wolfgang; Peters, René (2019-04-08). "Polyfunctional Bis‐Lewis‐Acid‐/Bis‐Triazolium Catalysts for Stereoselective 1,4‐Additions of 2‐Oxindoles to Maleimides". Angewandte Chemie International Edition. 58 (16): 5447–5451. doi:10.1002/anie.201814453. ISSN 1433-7851.
  7. ^ Willig, Felix; Lang, Johannes; Hans, Andreas C.; Ringenberg, Mark R.; Pfeffer, Daniel; Frey, Wolfgang; Peters, René (2019-07-31). "Polyfunctional Imidazolium Aryloxide Betaine/Lewis Acid Catalysts as Tools for the Asymmetric Synthesis of Disfavored Diastereomers". Journal of the American Chemical Society. 141 (30): 12029–12043. doi:10.1021/jacs.9b04902. ISSN 0002-7863.
  8. ^ Miskov‐Pajic, Vukoslava; Willig, Felix; Wanner, Daniel M.; Frey, Wolfgang; Peters, René (2020-11-02). "Enantiodivergent [4+2] Cycloaddition of Dienolates by Polyfunctional Lewis Acid/Zwitterion Catalysis". Angewandte Chemie International Edition. 59 (45): 19873–19877. doi:10.1002/anie.202009093. ISSN 1433-7851. PMC 7693193. PMID 32697020.{{cite journal}}: CS1 maint: PMC format (link)
  9. ^ Mechler, Melanie; Peters, René (2015-08-24). "Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts". Angewandte Chemie International Edition. 54 (35): 10303–10307. doi:10.1002/anie.201502930.
  10. ^ Schmid, Juliane; Junge, Thorsten; Lang, Johannes; Frey, Wolfgang; Peters, René (2019-04-08). "Polyfunctional Bis‐Lewis‐Acid‐/Bis‐Triazolium Catalysts for Stereoselective 1,4‐Additions of 2‐Oxindoles to Maleimides". Angewandte Chemie International Edition. 58 (16): 5447–5451. doi:10.1002/anie.201814453. ISSN 1433-7851.
  11. ^ Weiss, Matthias E.; Fischer, Daniel F.; Xin, Zhuo-qun; Jautze, Sascha; Schweizer, W. Bernd; Peters, René (2006-08-25). "Practical, Highly Active, and Enantioselective Ferrocenyl–Imidazoline Palladacycle Catalysts (FIPs) for the Aza-Claisen Rearrangement ofN-para-Methoxyphenyl Trifluoroacetimidates". Angewandte Chemie International Edition. 45 (34): 5694–5698. doi:10.1002/anie.200601731. ISSN 1433-7851.
  12. ^ Huang, Haoxi; Peters, René (2009-01-05). "A Highly Strained Planar-Chiral Platinacycle for Catalytic Activation of Internal Olefins in the Friedel-Crafts Alkylation of Indoles". Angewandte Chemie International Edition. 48 (3): 604–606. doi:10.1002/anie.200804944.
  13. ^ Fischer, Daniel F.; Barakat, Assem; Xin, Zhuo-qun; Weiss, Matthias E.; Peters, René (2009-09-07). "The Asymmetric Aza-Claisen Rearrangement: Development of Widely Applicable Pentaphenylferrocenyl Palladacycle Catalysts". Chemistry - A European Journal. 15 (35): 8722–8741. doi:10.1002/chem.200900712.
  14. ^ Schrapel, Carmen; Peters, René (2015-08-24). "Exogenous-Base-Free Palladacycle-Catalyzed Highly Enantioselective Arylation of Imines with Arylboroxines". Angewandte Chemie International Edition. 54 (35): 10289–10293. doi:10.1002/anie.201501846.
  15. ^ Pfeffer, Camilla; Probst, Patrick; Wannenmacher, Nick; Frey, Wolfgang; Peters, René (2022-08-26). "Direct Enantioselective Addition of Alkynes to Imines by a Highly Efficient Palladacycle Catalyst". Angewandte Chemie International Edition. 61 (35). doi:10.1002/anie.202206835. ISSN 1433-7851. PMC 9545068. PMID 35701311.{{cite journal}}: CS1 maint: PMC format (link)
  16. ^ Yu, Xin; Hu, Lingfei; Frey, Wolfgang; Lu, Gang; Peters, René (2022-10-17). "Stereoretentive Regio‐ and Enantioselective Allylation of Isoxazolinones by a Planar Chiral Palladacycle Catalyst". Angewandte Chemie International Edition. 61 (42). doi:10.1002/anie.202210145. ISSN 1433-7851.
  17. ^ Jautze, Sascha; Peters, René (2008-11-17). "Enantioselective Bimetallic Catalysis of Michael Additions Forming Quaternary Stereocenters". Angewandte Chemie International Edition. 47 (48): 9284–9288. doi:10.1002/anie.200803539. ISSN 1433-7851.
  18. ^ Weber, Manuel; Jautze, Sascha; Frey, Wolfgang; Peters, René (2010-09-08). "Bispalladacycle-Catalyzed Brønsted Acid/Base-Promoted Asymmetric Tandem Azlactone Formation−Michael Addition". Journal of the American Chemical Society. 132 (35): 12222–12225. doi:10.1021/ja106088v. ISSN 0002-7863.
  19. ^ Eitel, Simon H.; Jautze, Sascha; Frey, Wolfgang; Peters, René (2013). "Asymmetric Michael additions of α-cyanoacetates by soft Lewis acid/hard Brønsted acid catalysis: stereodivergency with bi- vs. monometallic catalysts". Chemical Science. 4 (5): 2218. doi:10.1039/c3sc50419k. ISSN 2041-6520.
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