About: Development of small focused libraries of supported amino alcohols as an efficient strategy for the optimization of enantioselective heterogeneous catalysts for the ZnEt2 addition to benzaldehyde

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About: Development of small focused libraries of supported amino alcohols as an efficient strategy for the optimization of enantioselective heterogeneous catalysts for the ZnEt2 addition to benzaldehyde Goto Sponge NotDistinct Permalink

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description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 2003 (uk) im März 2003 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en 2003 (fr)
publication date	wds:Q63209813-A4F96332-7475-4B91-B338-F79495025F97
publication date	2003-03-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q63209813-0A979003-45EF-4CC8-B0F5-2BFEC7E894C3 wds:Q63209813-0DE93CCA-CA9B-4710-AF78-CBA3DF29ECE8 wds:Q63209813-21027C5A-6EC9-4C24-8A63-B55384DBC440 wds:Q63209813-224BC46E-0DB1-404A-9B94-8A001C7C5835 wds:Q63209813-2FA3FA55-ADA1-4CD1-AB98-CF3298BFDC56 wds:Q63209813-35B63854-6763-41A1-A688-4A01E6357724 wds:Q63209813-36C7ECBA-D807-400E-8341-970E7FA21B15 wds:Q63209813-3E1AFF65-26E6-40A6-A31B-99B08EC4F5A0 wds:Q63209813-440A198A-CAE3-47B5-8A65-62A433904EB6 wds:Q63209813-4A6CD2BE-2ABC-4C2A-B53E-7B1883DFD701 wds:Q63209813-5519C022-B5BD-4016-8E8F-79635DD388AE wds:Q63209813-5B7B4939-2EF7-4E2F-A28B-55349FC3B7C5 wds:Q63209813-629971D6-B917-4BC7-A909-AE20C9F105A7 wds:Q63209813-66F74DDD-90BE-41A8-A18F-96C530479152 wds:Q63209813-6804CBD4-04D6-42EB-95BA-2D70CDB9CA75 wds:Q63209813-69D0AEFB-6A96-4AA3-9088-1A73C9840736 wds:Q63209813-6CA75491-A56B-4258-A16B-5B521E793569 wds:Q63209813-71ACF4D4-47BB-4AFD-A414-B1D055E89C86 wds:Q63209813-74DEFF9F-5182-46EA-AAA1-597082FA5358 wds:Q63209813-7661CA53-248A-4096-A134-D68B89541A7A wds:Q63209813-787334F2-1E06-4A74-9768-43FB3A71FF65 wds:Q63209813-84C27C46-0786-4DE0-ACCD-FD3A2C4225DC wds:Q63209813-902DCB0E-5E6F-4C46-B95F-CA591530FD83 wds:Q63209813-936E712E-13F5-444C-843A-6210B17B49D5 wds:Q63209813-9552BB7C-5CF2-499E-9835-C1E1C482214B wds:Q63209813-9C3D59E0-AFF5-42F9-BC3A-B3DF62204D16 wds:Q63209813-9FB97A4E-5C2A-42C7-8DBD-C3285FC2DCDB wds:Q63209813-AF01507F-364D-4214-9F70-CE9DAAD6645D wds:Q63209813-C6103265-60B9-40B6-9CA3-05DACDB55AD6 wds:Q63209813-C7A153F4-933A-4C86-89C9-A3EE0CE92C0E wds:Q63209813-C7DD5D4A-B64A-4805-B787-B7482C58E4FB wds:Q63209813-E58E76D9-A688-4409-A5B9-C2C4710D419C wds:Q63209813-E67C6727-6F6A-4CC9-899D-21337A32F505 wds:Q63209813-EB3B8E62-4C10-4CBA-8B63-FC50FACF3D9B wds:Q63209813-EBB060C0-3E43-4669-9771-6D6E2842ED3D wds:Q63209813-F271A1C1-C12B-45A5-83DA-27BDA709E5F9 wds:Q63209813-F3174427-3D66-4580-B112-BAB886E74E03 wds:Q63209813-FB458223-9D2C-42ED-835F-80E791F76718
cites work	Multi-step organic synthesis using solid-supported reagents and scavengers: a new paradigm in chemical library generation Time-Resolved IR-Thermographic Detection and Screening of Enantioselectivity in Catalytic Reactions. Measurement of Enantiomeric Excess by Kinetic Resolution and Mass Spectrometry A Method for High-Throughput Screening of Enantioselective Catalysts Combinatorial Chemistry for Ligand Development in Catalysis: Synthesis and Catalysis Screening of Peptidosulfonamide Tweezers on the Solid Phase Super-High-Throughput Screening of Enantioselective Catalysts by Using Capillary Array Electrophoresis Beyond Nature's Chiral Pool: Enantioselective Catalysis in Industry Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification Enantioselective addition of organozinc reagents to aldehydes Selection of enantioselective acyl transfer catalysts from a pooled peptide library through a fluorescence-based activity assay: an approach to kinetic resolution of secondary alcohols of broad structural scope Reaction microarrays: a method for rapidly determining the enantiomeric excess of thousands of samples. Schiff Base Catalysts for the Asymmetric Strecker Reaction Identified and Optimized from Parallel Synthetic Libraries Catalytic asymmetric organozinc additions to carbonyl compounds Enantioselective addition of diethylzinc to aldehydes catalyzed by N-(9-phenylfluoren-9-yl) beta-amino alcohols Towards more chemically robust polymer-supported chiral catalysts for the reactions of aldehydes with dialkylzincs How Important is the Inert Matrix of Supported Enantiomeric Catalysts? Reversal of Topicity with Two Polystyrene Backbones We would like to warmly thank Prof. J. M. J. Fréchet and Dr. F. Svec for technical advice. Financial support for this work was EMDee: an enzymatic method for determining enantiomeric excess Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes High Catalytic Activity of Chiral Amino Alcohol Ligands Anchored to Polystyrene Resins A quantum mechanics/molecular mechanics study of the highly enantioselective addition of diethylzinc to benzaldehyde promoted by (R)-2-piperidino-1,1,2-triphenylethanol Catalytic asymmetric epoxidation of unfunctionalized olefins using chiral (salen)manganese(III) complexes Polymer-supported Bis(oxazoline)-copper complexes as catalysts in cyclopropanation reactions Enantioselective Reduction of Ketones Catalyzed by Polymer-Supported Sulfonamide Using NaBH(4)/Me(3)SiCl (or BF(3) small middle dotOEt(2)) as Reducing Agent This work was supported by the Ministry of Sciences and Technology, the State Key Project of Polymer-supported BINOL ligand for the titanium-catalyzed diethylzinc addition to aldehydes: A remarkable positive influence of the support on the enantioselectivity of the catalyst Bis(oxazoline)copper complexes covalently bonded to insoluble support as catalysts in cyclopropanation reactions. New β-Amino Alcohols as Chiral Ligands for the Catalytic Enantioselective Reduction of Prochiral Ketones and the Nucleophilic Addition of Diethylzinc to Benzaldehyde Polymer-Grafted Ti−TADDOL Complexes. Preparation and Use as Catalysts in Diels−Alder Reactions Functionalized Cross-Linked Copolymers: A "C2 -Symmetric" Solid-Phase Catalyst for Enantioselective Reactions Looking glass chemistry Enantioselective reduction of oxime ethers with borane catalyzed by polymer-supported 2-piperazinemethanol FT-Raman as a simple tool for the fast monitoring of reactions on silica-supported reagents and catalysts: application to silica-bound prolinol and TADDOLs The use of NIR-FT-Raman spectroscopy for the characterization of polymer-supported reagents and catalysts Polymerisation vs. grafting in the preparation of polymer-supported aluminium catalysts for the Diels-Alder reaction: The role of the polymeric backbone A general route for the preparation of polymer-supported N-tosyl aminoalcohols and their use as chiral auxiliaries Immobilization of chiral ligands on polymer fibers by electron beam induced grafting and applications in enantioselective catalysis Engineering Catalysts for Enantioselective Addition of Diethylzinc to Aldehydes with Racemic Amino Alcohols: Nonlinear Effects in Asymmetric Deactivation of Racemic Catalysts Financial support from the National Natural Science Foundation of China, t Combinatorial development of chiral phosphoramidite-ligands for enantioselective conjugate addition reactions Catalysis by amino acid-derived tetracoordinate complexes: enantioselective addition of dialkylzincs to aliphatic and aromatic aldehydes
author name string	wds:Q63209813-35A1B9BE-0AB0-4752-8752-3C3A6D98E3B5 wds:Q63209813-789D005D-C8B2-4430-B918-23C829EB8DE4 wds:Q63209813-9520A716-D4D1-437B-A080-77EBD1555F2D wds:Q63209813-B02BB848-4A51-420B-BB06-284458928009 wds:Q63209813-C1E745F6-C4B8-44EB-8706-0AFD3E960C22 wds:Q63209813-EC3A51EA-27C1-427D-AA1A-25EBC9DBC887 wds:Q63209813-F28BC951-6D11-49F7-AC8D-E8D0C73FC179
author name string	M Isabel Burguete Santiago V Luis Manuel Collado Jürgen Martens Eduardo Garcı́a-Verdugo Marı́a J Vicent Nikolai Graf von Keyserling
rdfs:label	Development of small focused libraries of supported amino alcohols as an efficient strategy for the optimization of enantioselective heterogeneous catalysts for the ZnEt2 addition to benzaldehyde (en) Development of small focused libraries of supported amino alcohols as an efficient strategy for the optimization of enantioselective heterogeneous catalysts for the ZnEt2 addition to benzaldehyde (nl)
skos:prefLabel	Development of small focused libraries of supported amino alcohols as an efficient strategy for the optimization of enantioselective heterogeneous catalysts for the ZnEt2 addition to benzaldehyde (en)

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