Dr. Sami Lakhdar

Sami Lakhdar Dr. New address: Laboratoire de Chimie Moléculaire et Thio-organique UMR CNRS 6507 ENSICAEN-Université de Caen Basse-Normandie 6 Boulevard du Maréchal Juin 14050 Caen (France)
Awards
	Postdoc-Award by the Dr. Klaus Römer-Stiftung (2011).
Publications
	Structures and Reactivities of 2-Trityl- and 2-(Triphenylsilyl)pyrrolidine-Derived Enamines: Evidence for Negative Hyperconjugation with the Trityl Group H. Erdmann, F. An, P. Mayer, A. R. Ofial, S. Lakhdar, H. Mayr, J. Am. Chem. Soc. 2014, 136, 14263-14269. [download]
	Structures and Reactivities of Iminium Ions Derived From Substituted Cinnamaldehydes and Various Chiral Imidazolidin-4-ones F. An, S. Paul, J. Ammer, A. R. Ofial, P. Mayer, S. Lakhdar, H. Mayr, Asian J. Org. Chem. 2014, 3, 550-555. [download]
	Nichtbindende Wechselwirkungen in der Organokatalyse: Modulierung konformativer Diversität und Reaktivität im MacMillan-Katalysator Non-Covalent Interactions in Organocatalysis: Modulating Conformational Diversity and Reactivity in the MacMillan Catalyst M. C. Holland, S. Paul, W. B. Schweizer, K. Bergander, C. Mück-Lichtenfeld, S. Lakhdar, H. Mayr, R. Gilmour, Angew. Chem. 2013, 125, 8125-8129; Angew. Chem. Int. Ed. 2013, 52, 7967-7971. [deutsch-download] [english-download]
	A quantitative approach to nucleophilic organocatalysis H. Mayr, S. Lakhdar, B. Maji, A. R. Ofial, Beilstein J. Org. Chem. 2012, 8, 1458–1478. [download]
	Kinetics and mechanism of organocatalytic aza-Michael Additions: Direct observation of enamine intermediates S. Lakhdar, M. Baidya, H. Mayr, Chem. Commun. 2012, 48, 4504-4506. [download]
	Enamine aus Imidazolidinonen: Nucleophile mit geringer Reaktivität Imidazolidinone Derived Enamines: Nucleophiles with Low Reactivity S. Lakhdar, B. Maji, H. Mayr, Angew. Chem. 2012, 124, 5837-5840; Angew. Chem. Int. Ed. 2012, 51, 5739-5742. [deutsch-download][english-download]
	Nucleophilicity Parameters of Enamides and their Implications for Organocatalytic Transformations B. Maji, S. Lakhdar, H. Mayr, Chem. Eur. J. 2012, 18, 5732-5740. [download]
	Laserblitzphotolytische Erzeugung α,β-ungesättigter Iminium-Ionen Generation of α,β-Unsaturated Iminium Ions by Laser Flash Photolysis S. Lakhdar, J. Ammer, H. Mayr, Angew. Chem. 2011, 123, 10127-10130; Angew. Chem. Int. Ed. 2011, 50, 9953-9956 [deutsch-download][english-download]
	Counterion Effects in Iminium-Activated Electrophilic Aromatic Substitutions of Pyrroles S. Lakhdar, H. Mayr, Chem. Commun. 2011, 47, 1866-1868. [download]
	Kinetischer Nachweis der Bildung von Oxazolidinonen im stereogenen Schritt prolinkatalysierter Reaktionen Kinetic Evidence for Oxazolidinone Formation in the Stereogenic Step of Proline-Catalyzed Reactions T. Kanzian, S. Lakhdar, H. Mayr, Angew. Chem. 2010, 122, 9717-9720; Angew. Chem. Int. Ed. 2010, 49, 9526-9529. [deutsch-download][english-download]
	Reactivity Parameters for Rationalizing Iminium-Catalyzed Reactions S. Lakhdar, A. R. Ofial, H. Mayr, J. Phys. Org. Chem. 2010, 23, 886-892. [download]
	Wie werden Iminium-katalysierte Cyclopropanierungen durch elektrostatische Aktivierung gesteuert? How Does Electrostatic Activation Control Iminium Catalyzed Cyclopropanations? S. Lakhdar, R. Appel, H. Mayr, Angew. Chem. 2009, 121, 5134-5137; Angew. Chem. Int. Ed. 2009, 48, 5034-5037. [deutsch-download][english-download]
	Electrophilic Reactivities of α,β-Unsaturated Iminium Ions S. Lakhdar, T. Tokuyasu, H. Mayr, Angew. Chem. 2008, 120, 8851-8854; Angew. Chem. Int. Ed. 2008, 47, 8723-8726. [deutsch-download][english-download]
	Nucleophilic Reactivities of Indoles S. Lakhdar, M. Westermaier, F. Terrier, R. Goumont, T. Boubaker, A. R. Ofial, H. Mayr, J. Org. Chem. 2006, 71, 9088-9095. [download]