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Volumn 346, Issue 9-10, 2004, Pages 1101-1105

N-arenesulfonyl-2-aminomethylpyrrolidmes - Novel modular ligands and organocatalysts for asymmetric catalysis

Author keywords

Asymmetric catalysis; Diamines; Organic catalysis; Pyrrolidines; Sulfonamides

Indexed keywords

ALDEHYDE; AMINE; CARBOXYLIC ACID DERIVATIVE; DIAMINE DERIVATIVE; OXAZOLIDINONE DERIVATIVE; PROLINE DERIVATIVE; PYRROLIDINE DERIVATIVE;

EID: 5144230269     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200404098     Document Type: Article
Times cited : (117)

References (35)
  • 1
    • 0034750244 scopus 로고    scopus 로고
    • For reviews, see; a) B. List, Synlett 2001, 1675-1686; b) B. List, Tetrahedron 2002, 58, 5573-5590; c) R. O. Duthaler, Angew. Chem. Int. Ed. 2003, 42, 975-978; d) A. Córdova, Acc. Chem. Res. 2004, 37, 102-112.
    • (2001) Synlett , pp. 1675-1686
    • List, B.1
  • 2
    • 0037043180 scopus 로고    scopus 로고
    • For reviews, see; a) B. List, Synlett 2001, 1675-1686; b) B. List, Tetrahedron 2002, 58, 5573-5590; c) R. O. Duthaler, Angew. Chem. Int. Ed. 2003, 42, 975-978; d) A. Córdova, Acc. Chem. Res. 2004, 37, 102-112.
    • (2002) Tetrahedron , vol.58 , pp. 5573-5590
    • List, B.1
  • 3
    • 0037416272 scopus 로고    scopus 로고
    • For reviews, see; a) B. List, Synlett 2001, 1675-1686; b) B. List, Tetrahedron 2002, 58, 5573-5590; c) R. O. Duthaler, Angew. Chem. Int. Ed. 2003, 42, 975-978; d) A. Córdova, Acc. Chem. Res. 2004, 37, 102-112.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 975-978
    • Duthaler, R.O.1
  • 4
    • 1642415515 scopus 로고    scopus 로고
    • For reviews, see; a) B. List, Synlett 2001, 1675-1686; b) B. List, Tetrahedron 2002, 58, 5573-5590; c) R. O. Duthaler, Angew. Chem. Int. Ed. 2003, 42, 975-978; d) A. Córdova, Acc. Chem. Res. 2004, 37, 102-112.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 102-112
    • Córdova, A.1
  • 5
    • 1842792133 scopus 로고    scopus 로고
    • For recent examples of the catalytic use of proline, see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. Int. Ed. 2004, 43, 1109-1112; b) Y. Hayashi, J. Yamaguchi, T. Suniya, M. Shoji, Angew. Chem. Int. Ed. 2004, 43, 1112-1115.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1109-1112
    • Bøgevig, A.1    Sundén, H.2    Córdova, A.3
  • 6
    • 4243057730 scopus 로고    scopus 로고
    • For recent examples of the catalytic use of proline, see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. Int. Ed. 2004, 43, 1109-1112; b) Y. Hayashi, J. Yamaguchi, T. Suniya, M. Shoji, Angew. Chem. Int. Ed. 2004, 43, 1112-1115.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1112-1115
    • Hayashi, Y.1    Yamaguchi, J.2    Suniya, T.3    Shoji, M.4
  • 9
    • 0019612027 scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (1981) J. Mol. Catal. , vol.12 , pp. 265-319
    • Matteoli, U.1    Frediani, P.2    Bianchi, M.3    Botteghi, C.4    Gladiali, S.5
  • 10
    • 4243378570 scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (1992) Chem. Rev. , vol.92 , pp. 1051-1069
    • Zassinovich, G.1    Mestroni, G.2    Gladiali, S.3
  • 11
    • 0001951279 scopus 로고
    • (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (1992) Perspectives in Coordination Chemistry , pp. 463-486
    • Bäckvall, J.-E.1    Chowdhury, R.L.2    Karlsson, U.3    Wang, G.Z.4
  • 12
    • 0027943932 scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (1994) Synthesis , pp. 1007-1017
    • De Graauw, C.F.1    Peters, J.A.2    Van Bekkum, H.3    Huskens, J.4
  • 13
    • 0002123299 scopus 로고    scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (1997) Acc. Chem. Res. , vol.30 , pp. 97-102
    • Noyori, R.1    Hashiguchi, S.2
  • 14
    • 0033522739 scopus 로고    scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2045-2061
    • Palmer, M.J.1    Wills, M.2
  • 15
    • 0036605676 scopus 로고    scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (2002) J. Organomet. Chem. , vol.652 , pp. 105-111
    • Bäckvall, J.-E.1
  • 16
    • 0141800091 scopus 로고    scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (2003) Adv. Synth. Catal. , vol.345 , pp. 67-77
    • Everaere, K.1    Mortreux, A.2    Carpentier, J.-F.3
  • 17
    • 0038260520 scopus 로고    scopus 로고
    • For reviews, see: a) U. Matteoli, P. Frediani, M. Bianchi, C. Botteghi, S. Gladiali, J. Mol. Catal. 1981, 12, 265-319; b) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069; c) J.-E. Bäckvall, R. L. Chowdhury, U. Karlsson, G. Z. Wang, in: Perspectives in Coordination Chemistry, (Eds.: A. F. Williams, C. Floriani, A. E. Merbach), Helvetica Chimica Acta, Basel, 1992, pp. 463-486; d) C. F. de Graauw, J. A. Peters, H. van Bekkum, J. Huskens, Synthesis 1994, 1007-1017; e) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102; f) M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061; g) J.-E. Bäckvall, J. Organomet. Chem. 2002, 652, 105-111; h) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77; i) H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv. Synth. Catal. 2003, 345, 103-151.
    • (2003) Adv. Synth. Catal. , vol.345 , pp. 103-151
    • Blaser, H.-U.1    Malan, C.2    Pugin, B.3    Spindler, F.4    Steiner, H.5    Studer, M.6
  • 28
    • 0033534574 scopus 로고    scopus 로고
    • we employed conditions used in: b) M. J. Soth, J. S. Nowick, J. Org. Chem. 1999, 64, 276-281; c) A. Slaitas, E. Yeheskiely, Eur. J. Org. Chem. 2002, 14, 2391-2399.
    • (1999) J. Org. Chem. , vol.64 , pp. 276-281
    • Soth, M.J.1    Nowick, J.S.2
  • 29
    • 0036069515 scopus 로고    scopus 로고
    • we employed conditions used in: b) M. J. Soth, J. S. Nowick, J. Org. Chem. 1999, 64, 276-281; c) A. Slaitas, E. Yeheskiely, Eur. J. Org. Chem. 2002, 14, 2391-2399.
    • (2002) Eur. J. Org. Chem. , vol.14 , pp. 2391-2399
    • Slaitas, A.1    Yeheskiely, E.2
  • 35
    • 5144228835 scopus 로고    scopus 로고
    • [10a])
    • [10a]).


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