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Le cluster chemistry - catalyzed

Terms

15chemistry
16catalyzed
8nucleophilic
10substitution
4tolerant
4subgraph
7lactams
4isomorphism

Associations

Freq.WeightAssociation
55catalyzed - chemistry
44chemistry - substitution
66nucleophilic - substitution
44substitution - tolerant
44subgraph - tolerant
44subgraph - substitution
44lactams - nucleophilic
44isomorphism - tolerant
44isomorphism - substitution
44isomorphism - subgraph
44chemistry - nucleophilic
44catalyzed - substitution
44catalyzed - nucleophilic

Documents par ordre de pertinence
000140 (2015) Julien Lerouge [France] ; Pierre Le Bodic [États-Unis] ; Pierre Héroux [France] ; Sébastien Adam [France]GEM++: A Tool for Solving Substitution-Tolerant Subgraph Isomorphism
000407 (2013-08-20) Pierre Héroux [France] ; Pierre Le Bodic [États-Unis] ; Sébastien Adam [France]Datasets for the Evaluation of Substitution-Tolerant Subgraph Isomorphism
000545 (2013) Pierre Héroux [France] ; Pierre Le Bodic [États-Unis] ; Sébastien Adam [France]Datasets for the Evaluation of Substitution-Tolerant Subgraph Isomorphism
000573 (2012-06-16) Pierre Le Bodic [France] ; Pierre Héroux [France] ; Sébastien Adam [France] ; Yves Lecourtier [France]An integer linear program for substitution-tolerant subgraph isomorphism and its use for symbol spotting in technical drawings
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.
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).
000D48 (2008) Sébastien Comesse [France] ; Morgane Sanselme ; Adam DaïchNew and expeditious tandem sequence aza-Michael/intramolecular nucleophilic substitution route to substituted gamma-lactams: synthesis of the tricyclic core of (+/-)-martinellines.
000E28 (2008) Sebastien Comesse ; Morgane Sanselme ; Adam DaichChemInform Abstract: New and Expeditious Tandem Sequence Aza‐Michael/Intramolecular Nucleophilic Substitution Route to Substituted γ‐Lactams: Synthesis of the Tricyclic Core of (.+‐.)‐Martinellines.
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.
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.
001678 (2001) N. Hucher [France] ; Bernard Decroix [France] ; A. DaïchPi-aromatic and sulfur nucleophilic partners in cationic pi-cyclizations: intramolecular amidoalkylation and thioamidoalkylation cyclization via omega-carbinol lactams(1, 2).
001798 (2001) Nicolas Hucher ; Bernard Decroix [France] ; Adam DaichChemInform Abstract: π‐Aromatic and Sulfur Nucleophilic Partners in Cationic π‐Cyclizations: Intramolecular Amidoalkylation and Thioamidoalkylation Cyclization via ω‐Carbinol Lactams.
000066 (2016) Bahria Touati [France] ; Abderrahman El Bouakher [France] ; Catherine Taillier [France] ; Raja Ben Othman [Tunisie] ; Malika Trabelsi-Ayadi [Tunisie] ; Sylvain Antoniotti [France] ; Elisabet Du Ach [France] ; Vincent Dalla [France]Enolizable Carbonyls and N,O-Acetals: A Rational Approach for Room-Temperature Lewis Superacid-Catalyzed Direct α-Amidoalkylation of Ketones and Aldehydes.
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.
000160 (2015) Ronan Le Goff [France] ; Arnaud Martel ; Morgane Sanselme ; Ata Martin Lawson ; Adam Daïch ; Sébastien ComesseSimple access to highly functional bicyclic γ- and δ-lactams: origins of chirality transfer to contiguous tertiary/quaternary stereocenters assessed by DFT.
000337 (2014) Mélanie Hamon [France] ; Niall Dickinson ; Alice Devineau ; David Bolien ; Marie-José Tranchant ; Catherine Taillier ; Ivan Jabin ; David C. Harrowven ; Richard J. Whitby ; A. Ganesan ; Vincent DallaIntra- and intermolecular alkylation of N,O-acetals and π-activated alcohols catalyzed by in situ generated acid.
000395 (2013-11) Sigismund T A G. Melissen ; Vincent Tognetti [France] ; Georges Dupas [France] ; Julien Jouanneau [France] ; Guillaume Lê ; Laurent Joubert [France]A DFT study of the Al₂Cl₆-catalyzed Friedel-Crafts acylation of phenyl aromatic compounds.
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.
000518 (2013) Catalin Pintiala ; Ata Martin Lawson ; Sebastien Comesse ; Adam DaichChemInform Abstract: A Versatile Domino Process for the Synthesis of Substituted 3‐Aminomethylene‐chromanones and 2‐Pyridones Catalyzed by CsF.
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
000792 (2011) Sébastien Comesse [France] ; Arnaud Martel ; Adam DaïchDomino process optimized via ab initio study for an alternative access to bicyclic lactams.
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.
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
000E26 (2008) Mohamed M. Rammah ; Mohamed Othman ; Kabula Ciamala ; Carsten Strohmann ; Mohamed B. RammahChemInform Abstract: Silver‐Catalyzed Spirolactonization: First Synthesis of Spiroisoindole‐γ‐methylene‐γ‐butyrolactones.
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.
001104 (2006) Raja Ben Othman ; Till Bousquet ; Mohamed Othman ; Vincent DallaN‐Trialkylsilyl Bistrifluoromethanesulfonimides (R3SiNTf2) Are Powerful Catalyzed for the Highly Efficient α‐Amido Alkylation Reactions of Silicon‐Based Nucleophiles.
001137 (2006) Anthony Pesquet ; Adam Daich ; Bernard Decroix [France] ; Luc Van HijfteAcid‐Catalyzed Formation of Tricyclic N,S‐Acetals in Imidazolinone Series Based on the Use of the Unprecedented N‐Acyliminium Ion Cascade Reaction Involving Transposition, Heterocyclization and π‐Cyclization.
001240 (2005) Mickael Menand ; Vincent DallaTMAF‐Catalyzed Conjugate Addition of Oxazolidinone and Thiols.
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
001C54 (1998) A. Mamouni ; A. Daich ; Bernard Decroix [France]ChemInform Abstract: Palladium(II) Catalyzed Cyclization: A Facile Access to New Difunctionalized Thieno[3,2‐f]indolizine.
001E05 (1997) P. Pigeon ; Bernard Decroix [France]ChemInform Abstract: Benzothienoindolizidines via Intramolecular Aryl Radical Cyclization or Palladium‐Catalyzed Cyclization.
002251 (1993) Janine Szabo [France] ; Georges Szabo [France] ; Jacob Van Gestel [France] ; Daniel Cornet [France]Isomerization of n-butenes to isobutene catalyzed by fluorinated alumina

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