메뉴 건너뛰기




Volumn 7, Issue 3, 2003, Pages 420-426

Recent advances in the discovery of organometallic catalysts using high-throughput screening assays

Author keywords

[No Author keywords available]

Indexed keywords

METAL; ORGANOMETALLIC COMPOUND;

EID: 0037523446     PISSN: 13675931     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1367-5931(03)00056-5     Document Type: Review
Times cited : (57)

References (32)
  • 1
    • 0037036757 scopus 로고    scopus 로고
    • Isotopically chiral probes for in situ high-throughput asymmetric reaction analysis
    • 13C NMR spectrum.
    • 13C NMR spectrum.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9020-9021
    • Evans, M.A.1    Morken, J.P.2
  • 2
    • 0037521243 scopus 로고    scopus 로고
    • A practical NMR-based high-throughput assay for screening enantioselective catalysts and biocatalysts
    • Reetz M.T., Eipper A., Tielmann P., Mynott R. A practical NMR-based high-throughput assay for screening enantioselective catalysts and biocatalysts. Adv. Synth. Catal. 344:2002;1008-1016.
    • (2002) Adv. Synth. Catal. , vol.344 , pp. 1008-1016
    • Reetz, M.T.1    Eipper, A.2    Tielmann, P.3    Mynott, R.4
  • 4
    • 0037148060 scopus 로고    scopus 로고
    • Colour Indicator for enantiomeric excess and assignment of the configuration of the major enantiomer of an amino acid ester
    • van Delden RA, Feringa BL: Colour Indicator for enantiomeric excess and assignment of the configuration of the major enantiomer of an amino acid ester. Chem Commun 2002:174-175.
    • (2002) Chem Commun , pp. 174-175
    • Van Delden, R.A.1    Feringa, B.L.2
  • 6
    • 0037045239 scopus 로고    scopus 로고
    • Discovery of exceptionally efficient catalysts for solvent-free enantioselective hetero-Diels-Alder reaction
    • Long J., Hu J., Shen X., Ji B., Ding K. Discovery of exceptionally efficient catalysts for solvent-free enantioselective hetero-Diels-Alder reaction. J. Am. Chem. Soc. 124:2002;10-11.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10-11
    • Long, J.1    Hu, J.2    Shen, X.3    Ji, B.4    Ding, K.5
  • 8
    • 0037035284 scopus 로고    scopus 로고
    • Combinatorial development of chiral phosphoramidite-ligands for enantioselective conjugate addition reactions
    • Huttenloch O, Laxman E, Waldmann H: Combinatorial development of chiral phosphoramidite-ligands for enantioselective conjugate addition reactions. Chem Commun 2002:673-675.
    • (2002) Chem Commun , pp. 673-675
    • Huttenloch, O.1    Laxman, E.2    Waldmann, H.3
  • 9
    • 0037134205 scopus 로고    scopus 로고
    • A high-throughput screening protocol for fast evaluation of enantioselective catalysts
    • Wolf C., Hawes P.A. A high-throughput screening protocol for fast evaluation of enantioselective catalysts. J. Org. Chem. 67:2002;2727-2729.
    • (2002) J. Org. Chem. , vol.67 , pp. 2727-2729
    • Wolf, C.1    Hawes, P.A.2
  • 10
    • 0031929976 scopus 로고    scopus 로고
    • One-pot multi-substrate screening in asymmetric catalysis
    • Gao X., Kagan H.B. One-pot multi-substrate screening in asymmetric catalysis. Chirality. 10:1998;120-124.
    • (1998) Chirality , vol.10 , pp. 120-124
    • Gao, X.1    Kagan, H.B.2
  • 11
    • 0037012762 scopus 로고    scopus 로고
    • In situ enzymatic screening (ISES): A tool for catalyst discovery and reaction development
    • An HTS technique was developed by coupling an organic reaction with an aqueous enzymatic reaction in a biphasic system. Formation of product from the metal-catalyzed allylic amination that occurred in the organic layer was detected by UV-vis spectroscopy of the aqueous layer where an enzymatic reaction oxidized the ethanol by-product.
    • Berkowitz D.B., Bose M., Choi S. In situ enzymatic screening (ISES): a tool for catalyst discovery and reaction development. Angew Chem. Int. Ed. Engl. 41:2002;1603-1607 An HTS technique was developed by coupling an organic reaction with an aqueous enzymatic reaction in a biphasic system. Formation of product from the metal-catalyzed allylic amination that occurred in the organic layer was detected by UV-vis spectroscopy of the aqueous layer where an enzymatic reaction oxidized the ethanol by-product.
    • (2002) Angew Chem. Int. Ed. Engl. , vol.41 , pp. 1603-1607
    • Berkowitz, D.B.1    Bose, M.2    Choi, S.3
  • 12
    • 0037012758 scopus 로고    scopus 로고
    • Combinatorial libraries with p-functionalized aminopyridines: Ligands for the preparation of efficient C(Aryl)-Cl activation catalysts
    • Most of the novel catalysts screened for the Suzuki reaction were prepared by parallel synthetic methods.
    • Schareina T., Kempe R. Combinatorial libraries with p-functionalized aminopyridines: ligands for the preparation of efficient C(Aryl)-Cl activation catalysts. Angew Chem. Int. Ed. Engl. 41:2002;1521-1523 Most of the novel catalysts screened for the Suzuki reaction were prepared by parallel synthetic methods.
    • (2002) Angew Chem. Int. Ed. Engl. , vol.41 , pp. 1521-1523
    • Schareina, T.1    Kempe, R.2
  • 13
    • 0038589930 scopus 로고    scopus 로고
    • Parallel synthesis of aminomethylphosphine ligands
    • LaPointe A. Parallel synthesis of aminomethylphosphine ligands. J. Comb. Chem. 1:1998;101-104.
    • (1998) J. Comb. Chem. , vol.1 , pp. 101-104
    • LaPointe, A.1
  • 14
    • 0038535274 scopus 로고    scopus 로고
    • Solid-phase synthesis of an aminophosphine library
    • Ben-Aroya B.B.-N., Portnoy M. Solid-phase synthesis of an aminophosphine library. J. Comb. Chem. 3:2001;524-527.
    • (2001) J. Comb. Chem. , vol.3 , pp. 524-527
    • Ben-Aroya, B.B.-N.1    Portnoy, M.2
  • 15
    • 0035857568 scopus 로고    scopus 로고
    • Versatile approaches to the polymer-supported synthesis of bidentate phosphorus-containing ligands
    • The authors used solid-phase combinatorial techniques to synthesize homogeneous diphosphine ligands. This method allows access to a wide variety of ligand architectures.
    • Li G.Y., Fagan P.J., Watson P.L. Versatile approaches to the polymer-supported synthesis of bidentate phosphorus-containing ligands. Angew Chem. Int. Ed. Engl. 40:2001;1106 The authors used solid-phase combinatorial techniques to synthesize homogeneous diphosphine ligands. This method allows access to a wide variety of ligand architectures.
    • (2001) Angew Chem. Int. Ed. Engl. , vol.40 , pp. 1106
    • Li, G.Y.1    Fagan, P.J.2    Watson, P.L.3
  • 16
    • 0034837076 scopus 로고    scopus 로고
    • Screening of homogeneous catalysts by fluorescence resonance energy transfer. Identification of catalysts for room temperature heck reactions
    • Stambuli J.P., Stauffer S.R., Shaughnessy K.H., Hartwig J.F. Screening of homogeneous catalysts by fluorescence resonance energy transfer. Identification of catalysts for room temperature heck reactions. J. Am. Chem. Soc. 123:2001;2677-2678.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 2677-2678
    • Stambuli, J.P.1    Stauffer, S.R.2    Shaughnessy, K.H.3    Hartwig, J.F.4
  • 17
    • 0001560006 scopus 로고    scopus 로고
    • High-throughput screening studies of fiber-supported catalysts leading to room-temperature Suzuki coupling
    • Colacot T.J., Gore E.S., Kuber A. High-throughput screening studies of fiber-supported catalysts leading to room-temperature Suzuki coupling. Organometallics. 21:2002;3301-3304.
    • (2002) Organometallics , vol.21 , pp. 3301-3304
    • Colacot, T.J.1    Gore, E.S.2    Kuber, A.3
  • 18
    • 0036276975 scopus 로고    scopus 로고
    • 500 μM diameter beads as single reactors to screen organometallic catalysts: Discovery of a new supported catalyst for the hydrosilylation of ketones
    • Lavastre O., Morken J.P. 500. μM diameter beads as single reactors to screen organometallic catalysts: discovery of a new supported catalyst for the hydrosilylation of ketones New. J. Chem. 26:2002;745-749.
    • (2002) New. J. Chem. , vol.26 , pp. 745-749
    • Lavastre, O.1    Morken, J.P.2
  • 19
    • 0347928820 scopus 로고    scopus 로고
    • Triple tandem catalyst mixtures for the synthesis of polyethylenes with varying structures
    • Three polymerization catalysts were combined in one vessel with ethylene to produce branched polyethylene. To find the optimum mole ratios, the percentages of catalyst were varied using parallel pressure reactors coupled with automated high-throughput characterization of polymers by GPC and IR spectroscopy.
    • Komon Z.J.A., Diamond G.M., Leclerc M.K., Murphy V., Okazaki M., Bazan G.C. Triple tandem catalyst mixtures for the synthesis of polyethylenes with varying structures. J. Am. Chem. Soc. 124:2002;15280-15285 Three polymerization catalysts were combined in one vessel with ethylene to produce branched polyethylene. To find the optimum mole ratios, the percentages of catalyst were varied using parallel pressure reactors coupled with automated high-throughput characterization of polymers by GPC and IR spectroscopy.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 15280-15285
    • Komon, Z.J.A.1    Diamond, G.M.2    Leclerc, M.K.3    Murphy, V.4    Okazaki, M.5    Bazan, G.C.6
  • 20
    • 0037130676 scopus 로고    scopus 로고
    • A high-throughput optical screening method for the optimization of colloidal water oxidation catalysts
    • Morris N.D., Mallouk T.E. A high-throughput optical screening method for the optimization of colloidal water oxidation catalysts. J. Am. Chem. Soc. 124:2002;11114-11121.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11114-11121
    • Morris, N.D.1    Mallouk, T.E.2
  • 22
    • 0037024486 scopus 로고    scopus 로고
    • Quaternary Pt-based electrocatalyst for methanol oxidation by combinatorial electrochemistry
    • Choi W.C., Kim J.D., Woo S.I. Quaternary Pt-based electrocatalyst for methanol oxidation by combinatorial electrochemistry. Catal. Today. 74:2002;235-240.
    • (2002) Catal. Today , vol.74 , pp. 235-240
    • Choi, W.C.1    Kim, J.D.2    Woo, S.I.3
  • 23
    • 0037016124 scopus 로고    scopus 로고
    • Gas manifold for olefin polymerization and a convenient reactor design for the parallel screening of catalysts
    • Constable G.S., Gonzalez-Ruiz R.A., Kasi R.M., Coughlin E.B. Gas manifold for olefin polymerization and a convenient reactor design for the parallel screening of catalysts. Macromolecules. 35:2002;9613-9616.
    • (2002) Macromolecules , vol.35 , pp. 9613-9616
    • Constable, G.S.1    Gonzalez-Ruiz, R.A.2    Kasi, R.M.3    Coughlin, E.B.4
  • 24
    • 0036722470 scopus 로고    scopus 로고
    • Discovery of new fuel-lean NO reduction catalyst leads using combinatorial methodologies
    • Ozturk S., Senkan S. Discovery of new fuel-lean NO reduction catalyst leads using combinatorial methodologies. Appl. Catal. B. 38:2002;243-248.
    • (2002) Appl. Catal. B , vol.38 , pp. 243-248
    • Ozturk, S.1    Senkan, S.2
  • 25
    • 0036121961 scopus 로고    scopus 로고
    • Heterogeneous single-walled carbon nanotube catalyst discovery and optimization
    • Chen B.G.P., Han J., Meyyappan M., Cassell A.M. Heterogeneous single-walled carbon nanotube catalyst discovery and optimization. Chem. Mater. 14:2002;1891-1896.
    • (2002) Chem. Mater. , vol.14 , pp. 1891-1896
    • Chen, B.G.P.1    Han, J.2    Meyyappan, M.3    Cassell, A.M.4
  • 26
    • 0002826513 scopus 로고    scopus 로고
    • High-throughput screening system for catalytic hydrogen-producing materials
    • Jaramillo T.F., Ivanovskaya A., McFarland E.W. High-throughput screening system for catalytic hydrogen-producing materials. J. Comb. Chem. 4:2002;17-22.
    • (2002) J. Comb. Chem. , vol.4 , pp. 17-22
    • Jaramillo, T.F.1    Ivanovskaya, A.2    McFarland, E.W.3
  • 27
    • 0037173393 scopus 로고    scopus 로고
    • An approach to the construction of indexed libraries for the combinatorial selection of heterogeneous catalysts
    • Aramendía M.A., Borau V., Jiménez C., Marinas J.M., Romero F.J., Urbano F.J. An approach to the construction of indexed libraries for the combinatorial selection of heterogeneous catalysts. J. Catal. 209:2002;413-416.
    • (2002) J. Catal. , vol.209 , pp. 413-416
    • Aramendía, M.A.1    Borau, V.2    Jiménez, C.3    Marinas, J.M.4    Romero, F.J.5    Urbano, F.J.6
  • 28
    • 0036643470 scopus 로고    scopus 로고
    • C-C cross-coupling reactions for the combinatorial synthesis of novel organic materials
    • Schiedel M.-S., Briehn C.A., Bäuerle P. C-C cross-coupling reactions for the combinatorial synthesis of novel organic materials. J. Organomet. Chem. 653:2002;200-208.
    • (2002) J. Organomet. Chem. , vol.653 , pp. 200-208
    • Schiedel, M.-S.1    Briehn, C.A.2    Bäuerle, P.3
  • 29
    • 0036807331 scopus 로고    scopus 로고
    • High-throughput methods for the development of new catalytic asymmetric reactions
    • Traverse J.F., Snapper M.L. High-throughput methods for the development of new catalytic asymmetric reactions. Drug Discov. Today. 7:2002;1002-1012.
    • (2002) Drug Discov. Today , vol.7 , pp. 1002-1012
    • Traverse, J.F.1    Snapper, M.L.2
  • 30
    • 0037090667 scopus 로고    scopus 로고
    • New methods for the high-throughput screening of enantioselective catalysts and biocatalysts
    • Reetz M.T. New methods for the high-throughput screening of enantioselective catalysts and biocatalysts. Angew Chem. Int. Ed. Engl. 41:2002;1335-1338.
    • (2002) Angew Chem. Int. Ed. Engl. , vol.41 , pp. 1335-1338
    • Reetz, M.T.1
  • 31
    • 0036084211 scopus 로고    scopus 로고
    • Emerging methods for the rapid determination of enantiomeric excess
    • Finn M.G. Emerging methods for the rapid determination of enantiomeric excess. Chirality. 14:2002;534-540.
    • (2002) Chirality , vol.14 , pp. 534-540
    • Finn, M.G.1
  • 32
    • 0036603597 scopus 로고    scopus 로고
    • Proton-activated fluorescence as a tool for simultaneous screening of combinatorial chemical reactions
    • Evans C.A., Miller S.J. Proton-activated fluorescence as a tool for simultaneous screening of combinatorial chemical reactions. Curr. Opin. Chem. Biol. 6:2002;333-338.
    • (2002) Curr. Opin. Chem. Biol. , vol.6 , pp. 333-338
    • Evans, C.A.1    Miller, S.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.