Vincent Dalla And NotHaute-Normandie
List of bibliographic references
Number of relevant bibliographic references: 15.Ident. | Authors (with country if any) | Title |
---|---|---|
000517 | Liliana Boiaryna ; Mohamed Kamal El Mkaddem ; Catherine Taillier ; Vincent Dalla ; Mohamed Othman | ChemInform Abstract: Dual Hard/Soft Gold Catalysis: Intermolecular Friedel—Crafts‐Type α‐Amidoalkylation/Alkyne Hydroarylation Sequences by N‐Acyliminium Ion Chemistry. |
000675 | Moussa Saber ; Sebastien Comesse ; Vincent Dalla ; Pierre Netchitailo ; Adam Daich | ChemInform Abstract: Proximal Ester Assistance vs. Stereoelectronic Prohibition in Catalytic N‐Acyliminium Ion Reactions: Stereoselective Formation of Aza‐Heterocycles with Two Contiguous Quaternary‐Tertiary Stereocenters. |
000840 | Alice Devineau ; Guillaume Pousse ; Catherine Taillier ; Jerome Blanchet ; Jacques Rouden ; Vincent Dalla | ChemInform Abstract: One‐Pot Hydroxy Group Activation/Carbon—Carbon Bond Forming Sequence Using a Broensted Base/Broensted Acid System. |
000841 | Moussa Saber ; Sebastien Comesse ; Vincent Dalla ; Adam Daich ; Morgane Sanselme ; Pierre Netchitailo | ChemInform Abstract: Formal [3 + 2]‐Cycloaddition‐Based Approach Using Ethoxymethylene Malonate Derivatives: Novel and Expedient Access to Functionalized N‐Acyliminium Precursors. |
000992 | Alice Devineau ; Guillaume Pousse [France] ; Catherine Taillier ; Jérôme Blanchet [France] ; Jacques Rouden [France] ; Vincent Dalla | One‐Pot Hydroxy Group Activation/Carbon‐Carbon Bond Forming Sequence Using a Brønsted Base/Brønsted Acid System |
000994 | 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 | 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 | Raja Ben Othman ; Radouane Affani ; Marie-Jose Tranchant ; Sylvain Antoniotti ; Vincent Dalla ; Elisabet Dunach | ChemInform Abstract: N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon—Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4. |
000E30 | Melanie Hamon ; Mickael Menand ; Stephane Le Gac ; Michel Luhmer ; Vincent Dalla ; Ivan Jabin | ChemInform Abstract: Calix[6]tris(thio)ureas: Heteroditopic Receptors for the Cooperative Binding of Organic Ion Pairs. |
000F44 | Marie-Jose Tranchant ; Vincent Dalla | Reaction of Vinyl Triflates of α‐Keto Esters and Imides with Secondary Amines: Synthesis of α,β‐Diamino Carboxylic Acid Derivatives Through Aziridinium Ions. |
001082 | Fridrich Jr. Szemes ; Anthony Fousse ; Raja Ben Othman ; Till Bousquet ; Mohamed Othman ; Vincent Dalla | Towards 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. |
001104 | Raja Ben Othman ; Till Bousquet ; Mohamed Othman ; Vincent Dalla | N‐Trialkylsilyl Bistrifluoromethanesulfonimides (R3SiNTf2) Are Powerful Catalyzed for the Highly Efficient α‐Amido Alkylation Reactions of Silicon‐Based Nucleophiles. |
001120 | Marie-Jose Tranchant ; Charlotte Moine ; Raja Ben Othman ; Till Bousquet ; Mohamed Othman ; Vincent Dalla | Eco‐Friendly N‐Acyliminium Ion Chemistry: Solvent‐Free HNTf2 and TIPSOTf‐Catalyzed α‐Amidoalkylation of Silicon‐Based π‐Nucleophiles. |
001240 | Mickael Menand ; Vincent Dalla | TMAF‐Catalyzed Conjugate Addition of Oxazolidinone and Thiols. |
001255 | Raja Ben Othman ; Till Bousquet ; Anthony Fousse ; Mohamed Othman ; Vincent Dalla | Improving the Chemistry of N‐Acyliminium Ions: Nucleophilic Substitution Reactions of Pyrrolidinone Derivatives with Trialkylsilyl Nucleophiles Catalyzed by Triisopropylsilyltrifluoromethane Sulfonate (TIPSOTf). |
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