Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
about
Synthetic applications of fluorous solid-phase extraction (F-SPE)Comparison of the structures and stabilities of coiled-coil proteins containing hexafluoroleucine andt-butylalanine provides insight into the stabilizing effects of highly fluorinated amino acid side-chainsStructural basis for the enhanced stability of highly fluorinated proteinsFluorinated dendrimers as imaging agents for ¹⁹F MRI.Core-shell nanoreactors for efficient aqueous biphasic catalysis.Enrichment and analysis of peptide subsets using fluorous affinity tags and mass spectrometry.Synthetic polymer systems in drug development.Fluorous mixture synthesis of two libraries with hydantoin-, and benzodiazepinedione-fused heterocyclic scaffolds.Microwave-Enhanced High-Speed Fluorous Synthesis.Fluorous Synthesis of Hydantoin-, Piperazinedione-, and Benzodiazepinedione-Fused Tricyclic and Tetracyclic Ring Systems.Reactivity of carbon dioxide in hydrofluoroethers: a facile access to cyclic carbonates.Fluorous iminoalditols: a new family of glycosidase inhibitors and pharmacological chaperones.Electrochemistry in Media of Exceptionally Low Polarity: Voltammetry with a Fluorous Solvent.Highly selective detection of silver in the low ppt range with ion-selective electrodes based on ionophore-doped fluorous membranes.The asymmetric Heck and related reactions.Fluorous synthesis of heterocyclic systems.Potentiometric sensors based on fluorous membranes doped with highly selective ionophores for carbonateIon-selective electrodes with unusual response functions: simultaneous formation of ionophore-primary ion complexes with different stoichiometries.A recyclable fluorous organocatalyst for Diels-Alder reactionsFluorous 2,4-Dichloro-1,3,5-triazine (F-DCT) as Amide Coupling Agent.Highly efficient and selective enrichment of peptide subsets combining fluorous chemistry with reversed-phase chromatographyCoordinative properties of highly fluorinated solvents with amino and ether groups.Fluorous Chemistry in Pittsburgh: 1996-2008Development of fluorous Lewis acid-catalyzed reactions.Preparation of a Highly Fluorophilic Phosphonium Salt and its Use in a Fluorous Anion-Exchanger Membrane with High Selectivity for Perfluorinated AcidsHigh lipophilicity of perfluoroalkyl carboxylate and sulfonate: implications for their membrane permeability.De novo design of defined helical bundles in membrane environments.Fluorous enzymatic synthesis of phosphatidylinositides.Carbohydrate chemistry in drug discovery.Nitroxides: applications in synthesis and in polymer chemistry.The fluorous effect in biomolecular applications.Fluorine: a new element in protein design.Making expensive dirhodium(II) catalysts cheaper: Rh(II) recycling methods.Synthesis of binaphthyl based phosphine and phosphite ligands.Recent approaches for the direct use of elemental sulfur in the synthesis and processing of advanced materials.Design of phase-vanishing reactions.Direct experimental observation of mesoscopic fluorous domains in fluorinated room temperature ionic liquids.Methyl fluorosulfonyldifluoroacetate (MFSDA): An Underutilised Reagent for Trifluoromethylation.A fluorinated dendrimer achieves excellent gene transfection efficacy at extremely low nitrogen to phosphorus ratios.Pickering-emulsion inversion strategy for separating and recycling nanoparticle catalysts.
P2860
Q24649656-1FA9B819-0004-4F5B-BF85-5AB63D52CB1AQ27671776-DB85B499-A7FC-4369-B71A-213BE1FA578FQ27678017-49B9C017-36DE-4782-B440-D61C8AD4B558Q30660527-FD0C7D24-63A5-47A2-85BC-F86F9054EFA5Q30857468-6D3259F8-AC8F-4E1F-A6C2-9AEB4C2317C7Q33212901-4EC304C3-850A-48CA-A027-8612699894DCQ33218263-05B03F4C-6A03-4C3C-AEA4-9F30BCD23BE3Q33256858-291F5EF5-EAD0-4795-815B-7853683522F8Q33282991-F1C8428E-29D5-4AF5-A0CC-5BB34999C99CQ33342243-A9FAF660-6D0F-4062-833E-3427D78128B3Q33465256-BDA43CC1-4DA0-4B66-B024-E804C08E97B4Q33660528-9ADD61B4-FFA1-475F-B63F-2A7B46973848Q33706058-4264A2D0-7107-48B2-A6D6-D54F9B924173Q34138427-F2D50B2C-1B89-4802-8C5D-5D786D596F92Q34192997-A2252075-2D75-4258-B0DE-74990E6F239FQ35104061-7841B094-581B-4B04-8F22-59CC89AB83D8Q35629239-85C26F0A-33AA-4281-AF0C-9FC24B0A304FQ35690768-BF4797B0-94B4-4B47-9B19-6D044379A057Q35944489-9EBB8416-6D27-40FC-9418-5855A1DA0862Q36226062-15C5FC5D-B98B-4002-B07D-D2D0DF1F82A2Q36644910-EC49D625-FB58-452C-B910-9EA8C42F5D17Q36857044-A21CCEEE-DD9F-4142-B666-6E6BFE101B04Q36955905-7C9A8E46-D740-4D5A-ABF7-E5438110DF15Q36986498-5F5CC627-5607-4E33-9FF4-096C1269554FQ37005546-B21990EB-DAC7-4D64-B0A0-F4395D5C8722Q37147036-777F7C72-5A24-4344-9CC2-D1C0CEDB92AAQ37593332-56101808-72EA-4804-8EDE-5ABF9D50CAC2Q37712594-D26D8F65-5B59-4E63-871C-DF498A1565F2Q37853437-DCA1556E-0CA9-4852-8D99-04032A0B0F4FQ37871533-93FFA9ED-3020-45B0-8747-D2BC1A7734F2Q37892383-326913CA-B42B-4CE5-BAAD-A9694D116548Q37978552-19FC27D2-CB28-485A-883B-6A58AE1703A5Q37994587-49558BDB-590C-42A2-B570-F2AF17FB5386Q38115696-8644BFC7-F41C-49B1-9E00-F87D37B35E78Q38316178-7DF54A8C-09B9-4ACB-BDD5-ED1047660F05Q38467485-175BA3EB-5DC5-4ECA-8EAF-FB4F14D9A3CFQ38794506-9FBB41CE-80ED-44A9-B238-8007FC15C8D2Q38901379-3B638AEB-D259-4555-A2A5-3B8E41F2DA1CQ39035856-9DA62E1F-53B0-4ED0-9A16-F7A13F96ED84Q39217633-788A8646-610B-4E29-ABFB-0B50D7A644ED
P2860
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
description
1994 nî lūn-bûn
@nan
1994 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@ast
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@en
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@nl
type
label
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@ast
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@en
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@nl
prefLabel
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@ast
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@en
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.
@nl
P1433
P1476
Facile catalyst separation without water: fluorous biphase hydroformylation of olefins
@en
P2093
P356
10.1126/SCIENCE.266.5182.72
P407
P577
1994-10-01T00:00:00Z