Pucheault et al., 2010 - Google Patents
Task specific ionic liquids and task specific onium saltsPucheault et al., 2010
View PDF- Document ID
- 6893449348644982110
- Author
- Pucheault M
- Vaultier M
- Publication year
- Publication venue
- Ionic Liquids
External Links
Snippet
Task specific ionic liquids (TSILs), or more generally task specific onium salts (TSOSs), can be defined as an association of a cation and anion, one at least being organic, to which has covalently been attached through a linker a function that confers the assembly a specific …
- 150000003839 salts 0 title abstract description 88
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B53/00—Asymmetric syntheses
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B43/00—Formation or introduction of functional groups containing nitrogen
- C07B43/04—Formation or introduction of functional groups containing nitrogen of amino groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B61/00—Other general methods
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
- B01J31/0287—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre
- B01J31/0288—Phosphorus
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Pucheault et al. | Task specific ionic liquids and task specific onium salts | |
Tzschucke et al. | Modern separation techniques for the efficient workup in organic synthesis | |
Zhou et al. | Synthesis of C 1-symmetric chiral secondary diamines and their applications in the asymmetric copper (II)-catalyzed Henry (nitroaldol) reactions | |
Wu et al. | Biopolymer-metal complex wool–Pd as a highly active heterogeneous catalyst for Heck reaction in aqueous media | |
Šebesta et al. | Catalysts with ionic tag and their use in ionic liquids | |
Mane et al. | Pd/C-Catalyzed aminocarbonylation of aryl iodides via oxidative C–N bond activation of tertiary amines to tertiary amides | |
Arai et al. | Asymmetric Syn-Selective Henry Reaction Catalyzed by the Sulfonyldiamine− CuCl− Pyridine System | |
Golandaj et al. | Phosphonium salts in asymmetric catalysis: a journey in a decade's extensive research work | |
Gagliardo et al. | Catalytic Performance of Symmetrical and Unsymmetrical Sulfur‐Containing Pincer Complexes: Synthesis and Tandem Catalytic Activity of the First PCS‐Pincer Palladium Complex | |
CA2500206C (en) | Compositions containing ionic liquids and uses thereof, especially in organic synthesis | |
Fan et al. | Enantioselective Friedel–Crafts alkylation between nitroalkenes and indoles catalyzed by charge activated thiourea organocatalysts | |
Rodríguez‐Escrich et al. | Organocatalysis on tap: enantioselective continuous flow processes mediated by solid‐supported chiral organocatalysts | |
Szabó | Pincer complexes as catalysts in organic chemistry | |
Huo et al. | A novel liquid-phase strategy for organic synthesis using organic ions as soluble supports | |
Liu et al. | Linear polystyrene anchored L-proline, new recyclable organocatalysts for the aldol reaction in the presence of water | |
Candeias et al. | Making expensive dirhodium (II) catalysts cheaper: Rh (II) recycling methods | |
Mastrorilli et al. | Ionic liquids in palladium-catalyzed cross-coupling reactions | |
Bellemin-Laponnaz et al. | Synthesis and application of dynamic self-supported enantioselective catalysts | |
Zeng et al. | Synthesis of 1, 3-Amino Alcohols, 1, 3-Diols, Amines, and Carboxylic Acids from Terminal Alkynes | |
FR2857360A1 (en) | USE OF FUNCTIONALIZED ONIUM SALTS AS A SOLUBLE CARRIER FOR ORGANIC SYNTHESIS | |
Doherty | Homogeneous catalysis in ionic liquids | |
Kureshy et al. | Reusable Chiral Dicationic Chromium (III) Salen Catalysts for Aminolytic Kinetic Resolution of trans‐Epoxides | |
Hullio et al. | Designing, synthesis and applications of task specific ionic liquids | |
Kui et al. | Histidine-based salt as an ionic tag for proline: application in enantioselective cross aldol reaction in ionic liquids | |
Zhang | Fluorous organocatalysis |