DR ANTHONY MELVIN CRASTO,WorldDrugTracker, helping millions, A 90 % paralysed man in action for you, I am suffering from transverse mylitis and bound to a wheel chair,With death on the horizon, This will not stop me, Gods call only..........
DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 29Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK PHARMA at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contribution

Sunday 25 January 2015

Prof. Dr. Axel Jacobi von Wangelin

Prof. Dr. Axel Jacobi von Wangelin

Research Group , Axel Jacobi von Wangelin

Building CH, 13.1.82

Phone +49 (0)941 943-4802
Fax +49 (0)941 943-4617

E-mail: axel.jacobi@ur.de

http://www.uni-regensburg.de/index.html.en

Professor of Organic Chemistry (2011),

Heisenberg Group Leader (Cologne, 2011)

Emmy Noether Group Leader (Cologne, 2005-2010),

DAAD Postdoc (Stanford, B. M. Trost, 2003-2004),

Postdoc (Cardiff, K. J. Cavell, 2003),

Visiting Scientist (Degussa, 2002-2003),

Ph.D. (Rostock, M. Beller, 2002),

Visiting Scholar (Utah, J. A. Gladysz, 1999),

M.Sc. (Erlangen, J. A. Gladysz, 1998), B.Sc. (Erlangen, 1994)

Awards: ORCHEM Award of the Liebig Association (2012), Heisenberg Fellow of the DFG (2011), Science Award of the Industrieclub (2009), Thieme Journal Award (2007), Emmy Noether Fellow of the DFG (2005-2010), DAAD Fellow (2003-2004), Joachim Jungius Dissertation Award (2002)

Most cited publications:

1. Coming of Age: Sustainable Iron-Catalyzed Cross-Coupling Reactions
Times Cited: 285 (Web of Science Core Collection®)

2. Multicomponent coupling reactions for organic synthesis: Chemoselective reactions with amide-aldehyde mixtures
Times Cited: 173 (Web of Science Core Collection®)

3. Dinuclear Zn-catalyzed asymmetric alkynylation of unsaturated aldehydes
Times Cited: 155 (Web of Science Core Collection®)

more................

http://www.researcherid.com/ProfileView.action?returnCode=ROUTER.Unauthorized&queryString=KG0UuZjN5WlnUgQXxhsj4VTS5Hx4sF8eU%252BJqDvjTrPk%253D&SrcApp=CR&Init=Yes

Postal address
		Prof. Dr. Axel Jacobi von Wangelin
		Institut für Organische Chemie
		Universität Regensburg
		Universitätsstraße 31
		D-93053 Regensburg
		Germany

		Tel.: +49 (0)941 943-4802 (+49 (0)221 470-6122)
		Fax: +49 (0)941 943-4617
		e-mail: axel.jacobi@chemie.uni-regensburg.de

Iron-catalyzed olefin hydrogenation at 1 bar H2 with a FeCl3–LiAlH4catalyst

The scope and mechanism of a practical protocol for the iron-catalyzed hydrogenation of alkenes and alkynes at 1 bar H2 pressure were studied. The catalyst is formed from cheap chemicals (5 mol% FeCl3–LiAlH4, THF). A homogeneous mechanism operates at early stages of the reaction while active nanoparticles form upon ageing of the catalyst solution.

Iron-catalyzed olefin hydrogenation at 1 bar H2 with a FeCl3–LiAlH4catalyst

Tim N. Gieshoff,a Matteo Villa,a Alice Welther,a Markus Plois,b Uttam Chakraborty,b Robert Wolfb and Axel Jacobi von Wangelin*a

*Corresponding authors

aInstitute of Organic Chemistry, University of Regensburg, 93040 Regensburg, Germany

E-mail: axel.jacobi@ur.de

bInstitute of Inorganic Chemistry, University of Regensburg, 93040 Regensburg, Germany

Green Chem., 2015, Advance Article

DOI: 10.1039/C4GC02368D

http://pubs.rsc.org/en/Content/ArticleLanding/2015/GC/C4GC02368D?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+rss%2FGC+%28RSC+-+Green+Chem.+latest+articles%29#!divAbstract

regensburg........

University of Regensburg

The campus in 2009
The old administration
University canteen
A student protest occupies a lecture theater, December 2009
Library Philosophicum 2
Library entrance hall
Athletics track and stand
Ball sculpture
Vielberth building, faculty of business

Regensburg Wurstkueche. Wurstküche

Restaurant “Historisches Wurstkuchl” in Regensburg

Journals

H. Neumann, A. Jacobi von Wangelin, D. Gördes, A. Spannenberg, M. Beller, A New Multicomponent Coupling of Aldehydes, Amides, and Dienophiles: Atom-Efficient One-Pot Synthesis of Highly Substituted Cyclohexenes and Cyclohexadienes, J. Am. Chem. Soc. 2001, 123, 8398.
		A. Jacobi von Wangelin, H. Neumann, D. Gördes, A. Spannenberg, M. Beller, A Facile Three-Component Coupling Procedure for the Synthesis of Substituted Tetrahydroisoindole-1,3-diones from α,β-Unsaturated Aldehydes, Org. Lett. 2001, 3, 2895.
		H. Neumann, A. Jacobi von Wangelin, D. Gördes, A. Spannenberg, W. Baumann, M. Beller, Multicomponent Coupling Reactions of Aldehydes and Amides with Maleic Anhydride: Synthesis of 7-Oxo-6-azabicyclo[3.2.1]oct-2-ene-8-carboxylic Acid Derivatives, Tetrahedron 2002, 58, 2381.
		D. Gördes, H. Neumann, A. Jacobi von Wangelin, C. Fischer, K. Drauz, H.-P. Krimmer, M. Beller, Synthesis of N-Acetyl α-Aminobutyric Acid via Amidocarbonylation: A Case Study, Adv. Synth. Catal. 2003, 345, 510.
		A. Jacobi von Wangelin, H. Neumann, D. Gördes, S. Klaus, H. Jiao, A. Spannenberg, T. Krüger, C. Wendler, K. Thurow, N. Stoll, M. Beller, Unusual Coupling Reactions of Aldehydes and Alkynes: A Novel Preparation of Substituted Phthalic Acid Derivatives by Automated Synthesis, Chem. Eur. J.2003, 9, 2273.
		A. Jacobi von Wangelin, H. Neumann, D. Gördes, S. Klaus, D. Strübing, M. Beller, Multicomponent Coupling Reactions for Organic Synthesis: Chemoselective Reactions with Amide-Aldehyde Mixtures, Chem. Eur. J. 2003, 9, 4286.
		H. Neumann, A. Jacobi von Wangelin, S. Klaus, D. Strübing, D. Gördes, M. Beller, Anilines Made Easily: From Aldehydes to Tri-, Tetra-, and Penta-substituted Anilines in Two Steps, Angew. Chem. Int. Ed. 2003, 42, 4503.
		D. Strübing, H. Neumann, S. Klaus, A. Jacobi von Wangelin, D. Gördes, M. Beller, P. Braiuca, C. Ebert, L. Gardossi, U. Kragl, Enzymatic Resolution of 4-N-Phenylacetylamino Derivatives Obtained from Multicomponent Reactions Using PenG Amidase and In-Silico Studies, Tetrahedron 2004, 60, 683.
		D. Gördes, A. Jacobi von Wangelin, S. Klaus, H. Neumann, D. Strübing, S. Hübner, H. Jiao, W. Baumann, M. Beller, From a Spin-Off to the Advantageous Use in Diels-Alder Reactions: A Combined Synthetic, Spectroscopic and Computational Approach to N-(Dienyl)acylamines, Org. Biomol. Chem. 2004, 2, 845.
		H. Neumann, S. Klaus, M. Klawonn, D. Strübing, S. Hübner, D. Gördes, A. Jacobi von Wangelin, M. Lalk, M. Beller, A New Efficient Synthesis of Substituted Luminols Using Multicomponent Reactions, Z. Naturforsch. 2004, 59b, 431.
		S. Klaus, S. Hübner, H. Neumann, D. Strübing, A. Jacobi von Wangelin, D. Gördes, M. Beller, Second Generation Protocol for Multicomponent Coupling Reactions of Aldehydes, Amides, and Dienophiles, Adv. Synth. Catal. 2004, 346, 970.
		S. Klaus, H. Neumann, H. Jiao, A. Jacobi von Wangelin, D. Gördes, D. Strübing, S. Hübner, M. Hateley, C. Weckbecker, T. Riermeier, M. Beller, Efficient Hydroalkoxycarbonylation of Enamides to N-Acyl Amino Acid Esters: Theoretical Studies and Synthetic Applications, J. Organomet. Chem.2004, 689, 3685.
		D. Strübing, A. Jacobi von Wangelin, H. Neumann, D. Gördes, S. Hübner, S. Klaus, A. Spannenberg, M. Beller, Multicomponent Reaction of Aldehydes, Anhydrides, and Dienophiles: Synthesis of „Butterfly“-like Diazatetradecenes, Eur. J. Org. Chem. 2005, 107.
		A. Jacobi von Wangelin, H. Neumann, D. Gördes, S. Hübner, C. Wendler, S. Klaus, D. Strübing, A. Spannenberg, H. Jiao, L. El Firdoussi, K. Thurow, N. Stoll, M. Beller, Sequential Three-Component and Heck Reactions for the Synthesis of Phenanthridones, Synthesis 2005, 2029.
		S. Hübner, H. Neumann, A. Jacobi von Wangelin, S. Klaus, D. Strübing, H. Klein, M. Beller, Efficient One-Pot Synthesis of Substituted 1-Acylaminocyclohex-2-enes, Synthesis 2005, 2084, 2270.
		B. M. Trost, A. H. Weiss, A. Jacobi von Wangelin, A Dinuclear Zinc Catalyzed Asymmetric Alkynylation of Unsaturated Aldehydes, J. Am. Chem. Soc.2006, 128, 8.
		D. Strübing, H. Neumann, A. Jacobi von Wangelin, S. Klaus, S. Hübner, M. Beller, An Easy and General Protocol for Multicomponent Coupling Reactions of Amides, Aldehydes and Dienophiles, Tetrahedron 2006, 62, 10962.
		S. Hübner, H. Neumann, D. Michalik, S. Klaus, D. Strübing, A. Spannenberg, A. Jacobi von Wangelin, M. Beller, Three Component Reactions of α- and β-Bromo Aldehydes with Amides and Dienophiles – An Easy Way to Versatile 1-Amido-2-Cyclohexenes, Synlett 2007, 1085.
		S. Liebehentschel, J. Cvengros, A. Jacobi von Wangelin, Hydroxymethylpyridine Catalysts for the Enantioselective Alkynylation of Aldehydes,SYNLETT 2007, 2574.
		W. M. Czaplik, J.-M. Neudörfl, A. Jacobi von Wangelin, On the Quantitative Recycling of Raney-Nickel Catalysts On a Lab Scale, Green. Chem.2007, 1163.
		W. M. Czaplik, M. Mayer, A. Jacobi von Wangelin, Domino Iron Catalysis: Direct Aryl-Alkyl Cross-Coupling, Angew. Chem. Int. Ed. 2009, 48, 607-610.
		M. Mayer, W. M. Czaplik, A. Jacobi von Wangelin, On Cobalt-Catalyzed Biaryl Coupling Reactions, SYNLETT 2009, 2919-2923.
		W. M. Czaplik, M. Mayer, A. Jacobi von Wangelin, Direct Cobalt-Catalyzed Cross-Coupling Between Aryl and Alkyl Halides, SYNLETT 2009, 2931-2934.
		W. M. Czaplik, M. Mayer, J. Cvengro, A. Jacobi von Wangelin, Coming of Age: Sustainable Iron-Catalyzed Cross-Coupling Reactions,ChemSusChem 2009, 2, 396-417.
		R. Pérez-Ruiz, R. Fichtler, Y. Diaz Miara, M. Nicoul, D. Schaniel, H. Neumann, M. Beller, D. Blunk, A. G. Griesbeck, A. Jacobi von Wangelin, On the Photophysical Properties of New Luminol Derivatives and their Synthetic Phthalimide Precursors, J. Fluoresc. 2010, 20, 657-664.
		C. E. I. Knappke, J. M. Neudörfl, A. Jacobi von Wangelin, On New N-Heterocyclic Carbene Derived Alkylidene Imidazolines, Org. Biomol. Chem.2010, 8, 1695-1705
		C. E. I. Knappke, A. Jacobi von Wangelin, A Synthetic Double Punch: Suzuki-Miyaura Cross-Coupling Mates with CH Functionalization, Angew. Chem. 2010, 122, 3648-3650; Angew. Chem. Int. Ed. 2010, 49, 3568-3570.
		W. M. Czaplik, M. Mayer, S. Grupe, A. Jacobi von Wangelin, On Direct Iron-Catalyzed Cross-Coupling Reactions, Pure Appl. Chem. 2010, 82, 1545-1553.
		M. Mayer, W. M. Czaplik, A. Jacobi von Wangelin, Practical Iron-Catalyzed Allylations of Aryl Grignard Reagents, Adv. Synth. Catal. 2010, 352, 2147-2152.
		W. M. Czaplik, S. Grupe, M. Mayer, A. Jacobi von Wangelin, Practical Iron-Catalyzed Dehalogenation of Aryl Halides, Chem. Commun. 2010, 46, 6350-6352.
		C. E. I. Knappke, A. Jacobi von Wangelin, The Aminohydroxylation of Alkenes Breaks New Grounds, ChemCatChem 2010, 2, 1381-1383.
		W. M. Czaplik, M. Mayer, A. Jacobi von Wangelin, On Iron-Catalyzed Reductive Aryl-Alkenyl Cross-Coupling Reactions, ChemCatChem 2011, 3, 135.
		M. Mayer, A. Welther, A. Jacobi von Wangelin, Iron-Catalyzed Isomerizations of Olefins, ChemCatChem 2011, in print.
		R. Fichtler, J.-M. Neudörfl, A. Jacobi von Wangelin, Practical Three-Component Synthesis of Crowded Arenes with Donor–Acceptor Substitution,Org. Biomol. Chem. 2011, 9, 7224-7236.
		C. E. I. Knappke, A. Jacobi von Wangelin, 35 Years of Palladium-Catalyzed Cross-Coupling with Grignard Reagents: How far have we come?,Chem. Soc. Rev. 2011, 40, 4948-4962.
		M. Mayer, A. Welther, A. Jacobi von Wangelin, Iron-Catalyzed Isomerizations of Olefins, ChemCatChem 2011, 3, 1567-1571.
		C. E. I. Knappke, A. J. Arduengo, III, H. Jiao, J.-M. Neudörfl, A. Jacobi von Wangelin, On the Dual Role of N-Heterocyclic Carbenes as Bases and Nucleophiles in Reactions with Organic Halides, Synthesis 2011, 3784-3795.
		S. Gülak, A. Jacobi von Wangelin, Chlorostyrenes in Iron-Catalyzed Biaryl Coupling Reactions, Angew. Chem., accepted.
		A. K. Weber, A. Jacobi von Wangelin, Amine-Mediated Synthesis of Nitrocyclohexenes and Nitrocyclohexadienes, submitted.
		A. Welther, M. Bauer, M. Mayer, A. Jacobi von Wangelin, Iron(0) Particles: Catalytic Hydrogenations and Spectroscopic Studies, submitted.

		Books
		A. Jacobi von Wangelin, H. Neumann, D. Gördes, M. Beller, Amidocarbonylation of Aldehydes, in Transition Metals for Organic Synthesis (Ed. M. Beller, C. Bolm), Wiley-VCH: Weinheim, 2004, Ch. 2.5, p 133.
		A. Jacobi von Wangelin, Bismuth Reagents and Catalysts in Organic Synthesis, in Transition Metals for Organic Synthesis (Ed. M. Beller, C. Bolm), Wiley-VCH: Weinheim, 2004, Ch. 2.18, p 379.
		A. Jacobi von Wangelin, M. U. Frederiksen, Zinc-Mediated Reactions, in Transition Metals for Organic Synthesis (Ed. M. Beller, C. Bolm), Wiley-VCH: Weinheim, 2004, Ch. 3.7, p 519.
		A. Jacobi von Wangelin, H. Neumann, M. Beller, Carbonylation of Aldehydes, in Catalytic Carbonylation Reactions, Top. Organomet. Chem., Vol. 18, Springer: Berlin, 2006, p 207.
		R. Fichtler, R. Pérez-Ruiz, Y. Díaz Miara, H. Neumann, M. Beller, D. Blunk, A. G. Griesbeck, A. Jacobi von Wangelin, On the Photophysical Properties of New Luminol Derivatives - Electronic and Steric Substitution Effects, Conference Publication - IV Workshop on Sensors and Molecular Recognition 2010, Ch. 16, ISBN: 978-84-694-0303-7.

		Patents
		H. Neumann, A. Jacobi von Wangelin, D. Gördes, M. Beller, New Amido-Substituted Cyclohexadienes, Used as Precursors for Pharmaceutical, Agrochemical or Natural Substances, e.g. Pumiliotoxin, Lycoricidine or Narciclasine, are Prepared by Reacting Aldehyde, Amide and Alkyne in Solvent, DE 10137731 (2003).
		H. Neumann, A. Jacobi von Wangelin, D. Gördes, M. Beller, New Amido-Substituted Cyclohexenes, Used as Precursors for Pharmaceutical, Agrochemical or Natural Substances, e.g. Pumiliotoxin, Lycoricidine or Narciclasine, are Prepared by Reacting Unsaturated Aldehyde, Amide and Olefin, DE 10137739 (2003).
		H. Neumann, A. Jacobi von Wangelin, D. Gördes, M. Beller, New Amido-Substituted Cyclohexenes, Used as Precursors for Pharmaceutical, Agrochemical or Natural Substances, e.g. Pumiliotoxin, Lycoricidine or Narciclasine, are Prepared by Reacting Unsaturated Aldehyde, Amide and Olefin, DE 10137740 (2003).
		W. M. Czaplik, M. Gotta, M. Sundermeier, A. Jacobi von Wangelin, Katalytische Kreuzkupplung von Aryl-, Heteroaryl- oder Vinylhalogeniden mit Alkylhalogeniden, DE10 2008 016 702.9, DE10 2008 062 690.2.
		W. M. Czaplik, M. Gotta, M. Sundermeier, A. Jacobi von Wangelin, USSN 12/407,947.

		Other
		*Book recension:*
		P. Y. Bruice, Organische Chemie; Nachr. Chem. Tech. Lab. 2007, 55, 1132.
		B. Plietker, Iron Catalysis in Organic Chemistry; Angew. Chem. 2009, 121, 1562.
		M. Oestreich (Ed.), The Mizoroki-Heck Reaction, Nachr. Chem. 2009, 1030.
		*Conference reports:*
		Chem. Sus. Chem. 2008, 1, 565.
		Nachr. Chem. 2008, 56, 824.
		Der 7. Streich – Emmy-Noether in Köln, 19.-20. Februar 2010, Köln: Nachr. Chem. 2010, im Druck.
		*Chemie-Notizen:*
		Wir betreuen seit September 2011 die Rubrik "Chemie-Notizen" in den "Nachrichten aus der Chemie" und berichten über aktuelle Forschungsergebnisse zu katalytischen Themen.


		Talks
		Parallelized and Combinatorial Approaches to Multicomponent Reactions, BMBF-Seminar ‘Combinatorial Catalysis’, December 11, 2000, Rostock.
		Combinatorial Multicomponent and Carbonylation Reactions, BMBF-Seminar ‘Combinatorial Catalysis’, May 29, 2001, Warnemünde.
		Maximizing Synthetic Efficiency: The Development of New Multicomponent Reactions, ProjectHouse Catalysis Degussa AG, August 22, 2002, Frankfurt/Main.
		Maximizing Synthetic Efficiency: The Development of New Multicomponent Reactions, University of Rostock, December 2, 2002, Rostock.
		Homogeneous Catalysis – A Key Technology for the Environmentally Benign Synthesis of Fine Chemicals and Pharmaceuticals, ACHEMA, May 22,2003, Frankfurt/Main.
		Multicomponent and Catalytic Approaches to CC-Bond Forming Reactions, Institute of Organic Chemistry, University of the Saarland, January 8,2004, Saarbrücken.
		Multicomponent and Catalytic Approaches to CC-Bond Forming Reactions, Institute of Organic Chemistry, University of Cologne, March 15, 2004, Cologne.
		Multicomponent and Catalytic Approaches to CC-Bond Forming Reactions, Institute of Organic Chemistry, Technical University Munich, March 17,2004, Garching.
		New Concepts in Organo and Metal Catalysis, Dynamit-Nobel GmbH, February 26, 2007, Leverkusen.
		New Concepts in Organo and Metal Catalysis, Saltigo GmbH, September 24, 2007, Leverkusen.
		Neue Aspekte in Metall-katalysierten Kreuzkupplungen, University of Wuppertal, January 10, 2008, Wuppertal.
		Domino-Metall-Katalyse in Kreuzkupplungen, Chemiedozententagung, April 1, 2008, Kaiserslautern.
		New Aspects in Metal and Organo Catalysis, University of Bologna, April 10, 2008, Bologna.
		Multicomponent Syntheses of Carbo and Heterocycles, EU Project meeting, April 10, 2008, Bologna.
		New Aspects of Metal Catalyzed Cross Coupling Reactions, Leibniz Institute for Catalysis, August 28, 2008, Rostock.
		On New Reactions with N-Heterocyclic Carbenes, BioOrg 2008, September 30, 2008, Konstanz.
		In situ Umpolungsreaktionen: Metall-katalysierte Kreuzkupplungen und Reaktionen mit N-heterocyclischen Carbenen, Technical University Munich,December 3, 2008, Garching.
		New Aspects of Metal-Catalyzed Cross-Coupling Reactions, Merck KgaA, December 11, 2008, Darmstadt.
		New Aspects of Metal-Catalyzed Cross-Coupling Reactions, University of Leipzig, December 16, 2008, Leipzig.
		Preiswert und Sicher: Neue Aspekte Metall-katalysierter Kreuzkupplungsreaktionen, HLN-Kolloquium, Ruhr University Bochum, February 2, 2009, Bochum.
		Direkte Kreuzkupplungen, Emmy-Noether Annual Meeting, LMU Munich, February 14, 2009, München.
		Direkte Eisen-katalysierte Kreuzkupplungen, Chemiedozententagung, March 10, 2009, Göttingen.
		In situ Umpolungsreaktionen, University of Karlsruhe, May 5, 2009, Karlsruhe.
		Umpolung reactions: With metals and without, EPFL, May 14, 2009, Lausanne (CH).
		Zur Maximierung synthetischer Effizienz, Industrie-Club e.V., June 8, 2009, Düsseldorf.
		On Direct Iron-Catalyzed Cross-Coupling Reactions, ESOC 2009, July 13, 2009, Prag (CZ).
		Umpolung Reactions: With Metals and Without, EuCheMS Young Investigator Workshop, July 17, 2009, Liblice (CZ).
		On Direct Iron-Catalyzed Cross-Coupling Reactions, OMCOS 15, July 28, 2009, Glasgow (UK).
		In situ Umpolung Reactions: With Metals and Without, Bayer Schering Pharma, September 1, 2009, Wuppertal.
		On Direct Iron-Catalyzed Cross-Coupling Reactions, ISHHC XIV, September 14, 2009, Stockholm (S).
		Mach mit, mach’s nach, mach’s besser: Kleine Beiträge zu großartiger Chemie mit Metallen und ohne, Christmas Colloquium, University of Cologne, December 15, 2009.
		Eisen für alle, alles für Eisen: Neue Protokolle für Kupplungsreaktionen, University of Erlangen-Nuremburg, February 3, 2010.
		Ironing It Out: A Unifying Concept for Iron-Catalyzed Cross-Coupling Reactions, Annual Emmy Noether Meeting, University of Cologne, February 20, 2010.
		A Unifying Concept for Iron Catalyzed Cross Coupling Reactions, Chemiedozententagung, March 8, 2010, Gießen.
		Eine Spielwiese der Methodenentwicklung: Synthesen von und mit Aromaten für biologische, materialwissenschaftliche und synthetische Anwendungen, Martin Luther University Halle, May 4, 2010.
		Spielwiesen der Methodenentwicklung: Carbocyclen & Aromaten für biologische, materialwissenschaftliche und synthetische Anwendungen,University of Bielefeld, May 19, 2010.
		Spielwiesen der Methodenentwicklung: Carbocyclen & Aromaten für biologische, materialwissenschaftliche und synthetische Anwendungen,Boehringer-Ingelheim Pharma, May 21, 2010, Biberach.
		Eine Spielwiese für Katalysatoren: Synthesen funktionalisierter Carbocyclen für biologische, materialwissenschaftliche und synthetische Anwendungen, TU Darmstadt, June 7, 2010.
		The Aminocyclohexene Playground: Syntheses and Applications Abound, EU network meeting, June 24, 2010, Bratislava (SK).
		A Unifying Concept for Iron Catalyzed Cross Coupling Reactions, 3rd Sino-German Frontiers of Chemistry Symposium, August 13, 2010, Kloster Seeon.
		A Unifying Concept for Iron Catalyzed Cross Coupling Reactions, 3rd EuCheMS, September 1, 2010, Nürnberg.
		Metal- and Organo-Catalyzed Syntheses of Aromatic Materials, IIT Kanpur, October 4, 2010, Kanpur (IND).
		Against the Odds? Reductive Iron Catalysis in an Oxidative World, 14th Sigma-Aldrich Organic Synthesis Meeting, December 3, 2010, Sol Cress, Spa (B).
		Against the Odds? Reductive Iron Catalysis in an Oxidative World, FU Berlin, December 7, 2010.
		Against the Odds? Reductive Iron Catalysis in an Oxidative World, University of Mainz, December 16, 2010.
		Against the Odds? Reductive Iron Catalysis in an Oxidative World, RWTH Aachen, December 17, 2010.
		Iron & Magnesium – A perfect couple?, Chemetall, January 14, 2011, Frankfurt (Main).
		Organozinc Chemistry, Chemetall, January 14, 2011, Frankfurt (Main).
		Against the Odds? Reductive Iron Catalysis in an Oxidative World, University of Dortmund, January 18, 2011.
		Against the Odds? Reductive Iron Catalysis in an Oxidative World, University of Regensburg, January 24, 2011.
		Reduktive Eisen-Katalyse: Zur Entwicklung praktikabler Kreuzkupplungen und Hydrierungen, University of Bonn, February 3, 2011.
		Neue Reaktionen mit N-heterocyclischen Carbenen, Chemiedozententagung, Mainz, March 14, 2011.
		A Unifying Concept for Iron-Catalyzed Cross-Coupling and Reduction Reactions, 44. Jahrestreffen Deutscher Katalytiker, March 16, 2011, Weimar.
		Aminocyclohexenes - From an unwanted side product to a versatile synthetic platform, CATAFLU.OR: Organocatalysis Symposium, March 24, 2011, Bologna (I).
		Invading Palladium-Nickel Country: Iron Catalyzed Cross-Coupling and Reduction Reactions, University of Kaiserslautern, May 9, 2011.
		Invading Palladium-Nickel Country: Iron Catalyzed Cross-Coupling and Reduction Reactions, Boehringer Ingelheim, May 10, 2011.
		High Aims at a Low Price: Iron Catalyzed C-C and C-H Bond Formations, University of Hamburg, June 21, 2011.
		On Reductive Iron Catalysis, University of Göttingen, June 27, 2011.
		Spielwiesen der Methodenentwicklung: Metall- und Organo-Katalyse in der Synthese funktionalisierter Carbocyclen und Aromaten, Bayer Crop.Science, July 4, 2011, Monheim.