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List of bibliographic references indexed by chemistry

Number of relevant bibliographic references: 15.
Ident.Authors (with country if any)Title
000079 (2016) Dušan Berkeš [Slovaquie] ; Adam Daïch [France] ; Cécile Santos [France] ; Stéphanie Ballereau [France] ; Yves Génisson [France]Chemistry and Biology of HPAs: A Family of Ceramide Trafficking Inhibitors.
000517 (2013) Liliana Boiaryna ; Mohamed Kamal El Mkaddem ; Catherine Taillier ; Vincent Dalla ; Mohamed OthmanChemInform Abstract: Dual Hard/Soft Gold Catalysis: Intermolecular Friedel—Crafts‐Type α‐Amidoalkylation/Alkyne Hydroarylation Sequences by N‐Acyliminium Ion Chemistry.
000659 (2012) Reviewers Environmental Toxicology and Chemistry (15‐September 2010–28‐October 2011)
000670 (2012) Liliana Boiaryna ; El Mkaddem ; Taillier ; Dalla ; OthmanDual Hard/Soft Gold Catalysis: Intermolecular Friedel–Crafts‐Type α‐Amidoalkylation/Alkyne Hydroarylation Sequences by N‐Acyliminium Ion Chemistry
000994 (2010) Raja Ben Thman [Tunisie] ; Radouane Affani ; Marie-José Tranchant ; Sylvain Antoniotti ; Vincent Dalla [France] ; Elisabet Du Ach [France]N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon–Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4
000995 (2010) Raja Ben Thman [Tunisie] ; Radouane Affani ; Marie-José Tranchant ; Sylvain Antoniotti ; Vincent Dalla [France] ; Elisabet Du Ach [France]N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon–Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4
000A19 (2010) Raja Ben Othman ; Radouane Affani ; Marie-Jose Tranchant ; Sylvain Antoniotti ; Vincent Dalla ; Elisabet DunachChemInform Abstract: N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon—Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4.
000B36 (2009) F. Lique [France] ; M. Jorfi ; P. Honvault ; P. Halvick ; S Y Lin ; H. Guo ; D Q Xie ; P J Dagdigian ; J. Kłos ; M H AlexanderO+OH-->O(2)+H: A key reaction for interstellar chemistry. New theoretical results and comparison with experiment.
000C35 (2009) Abderrahmane Hadou ; Abdulkareem Hamid ; Hilarion Mathouet ; Mohamed-Fadel Deida ; Adam DaichChemInform Abstract: An Easy Access to the Exocyclic Lactams Analogous of the Central Nervous System Active Tricyclic Nitroxapine, Mianserine and Chlothiapine Agents Using N‐Acyliminium Chemistry.
000E14 (2008) Stéphane Le Ac [France] ; Jérôme Marrot [France] ; Ivan Jabin [Belgique]Highly Selective Synthesis of a 1,3,5‐Tris‐Protected Calix[6]arene‐Type Molecular Platform through Coordination and Host–Guest Chemistry
001082 (2006) Fridrich Jr. Szemes ; Anthony Fousse ; Raja Ben Othman ; Till Bousquet ; Mohamed Othman ; Vincent DallaTowards Simplifying the Chemistry of N‐Acyliminium Ions: A One‐Pot Protocol for the Preparation of 5‐Acetoxy Pyrrolidin‐2‐ones and 2‐Acetoxy N‐Alkoxycarbonyl Pyrrolidines from Imides.
001120 (2006) Marie-Jose Tranchant ; Charlotte Moine ; Raja Ben Othman ; Till Bousquet ; Mohamed Othman ; Vincent DallaEco‐Friendly N‐Acyliminium Ion Chemistry: Solvent‐Free HNTf2 and TIPSOTf‐Catalyzed α‐Amidoalkylation of Silicon‐Based π‐Nucleophiles.
001255 (2005) Raja Ben Othman ; Till Bousquet ; Anthony Fousse ; Mohamed Othman ; Vincent DallaImproving the Chemistry of N‐Acyliminium Ions: Nucleophilic Substitution Reactions of Pyrrolidinone Derivatives with Trialkylsilyl Nucleophiles Catalyzed by Triisopropylsilyltrifluoromethane Sulfonate (TIPSOTf).
001269 (2005) Armelle Cul ; Adam Daich ; Bernard Decroix [France] ; Gerard Sanz ; Luc Van HijfteAccess to the New Isoindolo[1,3]benzothiazocinones via the Combination of N‐Acyliminium Chemistry and Friedel—Crafts Type π‐Cyclization.
001586 (2002) Maria Inês Baeta Neves [France] ; Victor Oliva [France] ; Béchir Mrabet [France] ; Carole Connan [France] ; Mohamed M. Chehimi [France] ; Michel Delamar [France] ; Simon Hutton [Royaume-Uni] ; Adam Roberts [Royaume-Uni] ; Karim Benzarti [France]Surface chemistry of cement pastes: a study by x‐ray photoelectron spectroscopy

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