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Volumn 352, Issue 2-3, 2010, Pages 281-287

Synthesis and application of polymer-supported chiral Brønsted acid organocatalysts

Author keywords

BINOL phosphate; Heterogeneous catalysis; Immobilization; Organocatalysis; Polymers

Indexed keywords


EID: 77149179738     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.200900746     Document Type: Article
Times cited : (115)

References (136)
  • 1
    • 0003933276 scopus 로고
    • Chiral Reactions
    • For reviews on polymer-supported catalysts, see: a, Eds, V. Dubois, G. Jannes, Plenum, New York
    • For reviews on polymer-supported catalysts, see: a) H.-U. Blaser, B. Pugin, Chiral Reactions, in: Heterogeneous Catalysis, (Eds.: V. Dubois, G. Jannes), Plenum, New York, 1995, p 33;
    • (1995) Heterogeneous Catalysis , pp. 33
    • Blaser, H.-U.1    Pugin, B.2
  • 2
    • 0035648363 scopus 로고    scopus 로고
    • b) A. Baiker, Chimia 2001, 55, 796;
    • (2001) Chimia , vol.55 , pp. 796
    • Baiker, A.1
  • 3
    • 0003492617 scopus 로고    scopus 로고
    • Eds, D. E. De Vos, I. F. J. Vankelecom, P. A. Jacobs, Wiley-VCH, Weinheim, Germany
    • c) Chiral Catalyst Immobilization and Recycling, (Eds.: D. E. De Vos, I. F. J. Vankelecom, P. A. Jacobs), Wiley-VCH, Weinheim, Germany, 2000;
    • (2000) Chiral Catalyst Immobilization and Recycling
  • 5
    • 0036811776 scopus 로고    scopus 로고
    • special issue: Recoverable Catalysts and Reagents, (Ed.: J. A. Gladysz), Chem. Rev. 2002, 102, 3215;
    • e) special issue: Recoverable Catalysts and Reagents, (Ed.: J. A. Gladysz), Chem. Rev. 2002, 102, 3215;
  • 6
    • 77149135373 scopus 로고    scopus 로고
    • special issue: Polymer Supported Catalysts and Reagents in Synthetic Organic Chemistry, (Ed.: K. Janda), Bioorg. Med. Chem. Lett. 2002, 12, 1791;
    • f) special issue: Polymer Supported Catalysts and Reagents in Synthetic Organic Chemistry, (Ed.: K. Janda), Bioorg. Med. Chem. Lett. 2002, 12, 1791;
  • 10
    • 77149168874 scopus 로고    scopus 로고
    • for recoverable, soluble polymer-supported organic catalysts, see:, Eds. M. T. Reetz, B. List, S. Jaroch, H. Weinmann, Springer, Berlin, Heidelberg
    • j) for recoverable, soluble polymer-supported organic catalysts, see: M. Benaglia, Ernst Schering Foundation Symposium Proceedings, (Eds. M. T. Reetz, B. List, S. Jaroch, H. Weinmann), Springer, Berlin, Heidelberg, 2007 p 299.
    • (2007) Ernst Schering Foundation Symposium Proceedings , pp. 299
    • Benaglia, M.1
  • 11
    • 0001644556 scopus 로고    scopus 로고
    • For reviews on organocatalysis, see a
    • For reviews on organocatalysis, see a) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840;
    • (2001) Angew. Chem , vol.113 , pp. 3840
    • Dalko, P.I.1    Moisan, L.2
  • 15
    • 4143094833 scopus 로고    scopus 로고
    • special issue: Asymmetric Organocatalysts, (Eds.: K. N. Houk, B. List), Acc. Chem. Res. 2004, 37, 487;
    • c) special issue: Asymmetric Organocatalysts, (Eds.: K. N. Houk, B. List), Acc. Chem. Res. 2004, 37, 487;
  • 16
    • 47749122232 scopus 로고    scopus 로고
    • Eds, A. Berkessel, H. Gröger, Wiley-VCH, Weinheim
    • d) Asymmetric Organocatalysis, (Eds.: A. Berkessel, H. Gröger), Wiley-VCH, Weinheim 2005;
    • (2005) Asymmetric Organocatalysis
  • 21
    • 0033600691 scopus 로고    scopus 로고
    • Examples for the immobilization of catalysts derived from Cinchona alkaloids, see: a R. Alvarez, M.-A. Hourdin, C. Cavè, J. D'Angelo, P. Chaminade, Tetrahedron Lett. 1999, 40, 7091;
    • Examples for the immobilization of catalysts derived from Cinchona alkaloids, see: a) R. Alvarez, M.-A. Hourdin, C. Cavè, J. D'Angelo, P. Chaminade, Tetrahedron Lett. 1999, 40, 7091;
  • 26
    • 0003554758 scopus 로고    scopus 로고
    • Examples for immobilization of catalysts derived from amino acids, see: a
    • Examples for immobilization of catalysts derived from amino acids, see: a) M. S. Sigman, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 4901;
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 4901
    • Sigman, M.S.1    Jacobsen, E.N.2
  • 45
    • 34548414019 scopus 로고    scopus 로고
    • Example for the immobilization of heterazolium salts: K. Zeitler, I. Mager, Adv. Synth. Catal. 2007, 349, 1851.
    • Example for the immobilization of heterazolium salts: K. Zeitler, I. Mager, Adv. Synth. Catal. 2007, 349, 1851.
  • 46
    • 33745683614 scopus 로고    scopus 로고
    • Examples for the immobilization of TEMPO, see: a
    • Examples for the immobilization of TEMPO, see: a) A. Gheorghe, A. Matsuno, O. Reiser, Adv. Synth. Catal. 2006, 348, 1016;
    • (2006) Adv. Synth. Catal , vol.348 , pp. 1016
    • Gheorghe, A.1    Matsuno, A.2    Reiser, O.3
  • 49
    • 33745683617 scopus 로고    scopus 로고
    • For reviews on the application of chiral BINOL derived phosphoric acids, see: a
    • For reviews on the application of chiral BINOL derived phosphoric acids, see: a) T. Akiyama, J. Itoh, K. Fuchibe, Adv. Synth. Catal. 2006, 348, 999;
    • (2006) Adv. Synth. Catal , vol.348 , pp. 999
    • Akiyama, T.1    Itoh, J.2    Fuchibe, K.3
  • 52
  • 54
    • 77149124677 scopus 로고    scopus 로고
    • Examples for the application of chiral phosphoric acid diesters, from 2008: a J. Jiang, J. Yu, X.-X. Sun, Q.-Q. Rao, L.-Z. Gong, Angew. Chem. 2008, 120, 2492;
    • Examples for the application of chiral phosphoric acid diesters, from 2008: a) J. Jiang, J. Yu, X.-X. Sun, Q.-Q. Rao, L.-Z. Gong, Angew. Chem. 2008, 120, 2492;
  • 84
    • 77149153188 scopus 로고    scopus 로고
    • Selected examples on asymmetric catalysis employing BINOL phosphoric acids from our laboratory: a M. Rueping, E. Sugiono, C. Azap, Angew. Chem. 2006, 118, 2679;
    • Selected examples on asymmetric catalysis employing BINOL phosphoric acids from our laboratory: a) M. Rueping, E. Sugiono, C. Azap, Angew. Chem. 2006, 118, 2679;
  • 101
  • 105
    • 38049089797 scopus 로고    scopus 로고
    • For reviews on organocatalytic transfer hydrogenation with Hantzsch esters, see: a
    • For reviews on organocatalytic transfer hydrogenation with Hantzsch esters, see: a) S. G. Ouellet, A. M. Walji, D. W. C. Macmillan, Acc. Chem. Res. 2007, 40, 1327;
    • (2007) Acc. Chem. Res , vol.40 , pp. 1327
    • Ouellet, S.G.1    Walji, A.M.2    Macmillan, D.W.C.3
  • 109
    • 25444480017 scopus 로고    scopus 로고
    • For asymmetric Brønsted acid catalyzed transfer hydrogenations, see: a
    • For asymmetric Brønsted acid catalyzed transfer hydrogenations, see: a) M. Rueping, C. Azap, E. Sugiono, T. Theissmann, Synlett 2005, 2367;
    • (2005) Synlett , pp. 2367
    • Rueping, M.1    Azap, C.2    Sugiono, E.3    Theissmann, T.4
  • 136
    • 77149167894 scopus 로고    scopus 로고
    • A detailed experimental procedure is given in the Supporting Information
    • A detailed experimental procedure is given in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.