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Volumn 38, Issue 3, 1999, Pages 383-386

High-yielding rotaxane synthesis with an anion template

Author keywords

Host guest chemistry; Nucleophilic substitutions; Rotaxanes; Supramolecular chemistry; Template synthesis

Indexed keywords

ROTAXANE; TAXANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037747617     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19990201)38:3<383::AID-ANIE383>3.0.CO;2-H     Document Type: Article
Times cited : (193)

References (62)
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
    • Catenanes, Rotaxanes, Knots
    • Sauvage, J.P.1
  • 7
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Born, M.1    Ritter, H.2
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
    • (1997) Chem. Commun. , pp. 897-898
    • Hamilton, D.G.1    Sanders, J.K.M.2    Davies, J.E.3    Clegg, W.4    Teat, S.J.5
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413-1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
    • (1997) Chem. Commun. , pp. 1413-1414
    • Harada, A.1    Li, J.2    Kamachi, M.3
  • 10
    • 0000086115 scopus 로고    scopus 로고
    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
    • (1997) Angew. Chem. , vol.109 , pp. 2618-2621
    • Herrmann, W.1    Schneider, M.2    Wenz, G.3
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Reviews: a) G. Schill, Catenanes, Rotaxanes, and Knots, Academic Press, New York, 1971; b) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2825; c) H. W. Gibson in Large King Molecules (Ed.: J. A. Semlyen), Wiley, Chichester, 1996, pp. 191-262; d) R. Jäger, F. Vögtle, Angew. Chem. 1997, 109, 966-980; Angew. Chem. Int. Ed. Engl. 1997, 36, 930-944; e) Catenanes, Rotaxanes, Knots (Ed.: J. P. Sauvage), WILEY-VCH, in press. For recent reports, see M. Born, H. Ritter, Adv. Mater. 1996, 8, 149-151; D. G. Hamilton, J. K. M. Sanders, J. E. Davies, W. Clegg, S. J. Teat. Chem. Commun. 1997, 897-898; A. Harada, J. Li, M. Kamachi, Chem. Commun. 1997, 1413- 1414; W. Herrmann, M. Schneider, G. Wenz, Angew. Chem. 1997, 109, 2618-2621; Angew. Chem. Int. Ed. Engl. 1997, 36, 2511-2514; C. Gong, H. W. Gibson, Angew. Chem. 1998, 110, 323-327; Angew. Chem. Int. Ed. 1998, 37, 310-314; A. G. Kolchinski, N. W. Alcock, R. A. Roesner, D. H. Busch, Chem. Commun. 1998, 1437-1438; M. Fujita, M. Aoyagi, F. Ibukuro, K. Ogura, K. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 611-612; D. A. Leigh, A. Murphy, J. P. Smart, M. S. Deleuze, F. Zerbetto, J. Am. Chem. Soc. 1998, 120, 6458-6467; N. Armaroli, F. Diederich, C. O. Dietrich-Buchecker, L. Flamigni, G. Marconi, J.-F. Nierengarten, J.-P. Sauvage, Chem. Eur. J. 1998, 4, 406- 416; P. R. Ashton, M. C. T. Fyfe, M.-V. Martínez-Díaz, S. Menzer, C. Schiavo, J. F. Stoddart, A. J. P. White, D. J. Williams, Chem. Eur. J. 1998, 4, 1523-1534; T. Dünnwald, A. H. Parham, F. Vögtle, Synthesis 1998, 3, 339-348.
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    • Vögtle, F.1    Dünnwald, T.2    Schmidt, T.3
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    • 0344644429 scopus 로고    scopus 로고
    • thesis, University of Bonn
    • S. Ottens-Hildebrandt, S. Meier, M. Nieger, F. Vögtle, E. Weber, Supramol. Chem. 1995, 5, 133-138; F. Vögtle, T. Dünnwald, T. Schmidt, Acc. Chem. Res. 1996, 29, 451-460; S. Braschohs, thesis, University of Bonn, 1998. In catenanes derived from these lactams. however, one amide group of each ring is inverted and the carbonyl points inwards to provide additional hydrogen bonds: S. Ottens- Hildebrandt, M. Nieger, K. Rissanen, J. Rouvinen, S. Meier, G. Harder, F. Vögtle, J. Chem. Soc. Chem. Commun. 1995, 777-778; H. Adams, F. J. Carver, C. A. Hunter, J. Chem. Soc. Chem. Commun. 1995, 809-810. A rotaxane was reported where one amide bond also seems to be inverted: D. A. Leigh, A. Murphy, J. P. Smart, A. M. Z. Slawin. Angew. Chem. 1997, 109, 752-756; Angew. Chem. Int. Ed. Engl. 1997, 36, 752-756.
    • (1998)
    • Braschohs, S.1
  • 42
    • 37049086821 scopus 로고
    • S. Ottens-Hildebrandt, S. Meier, M. Nieger, F. Vögtle, E. Weber, Supramol. Chem. 1995, 5, 133-138; F. Vögtle, T. Dünnwald, T. Schmidt, Acc. Chem. Res. 1996, 29, 451-460; S. Braschohs, thesis, University of Bonn, 1998. In catenanes derived from these lactams. however, one amide group of each ring is inverted and the carbonyl points inwards to provide additional hydrogen bonds: S. Ottens-Hildebrandt, M. Nieger, K. Rissanen, J. Rouvinen, S. Meier, G. Harder, F. Vögtle, J. Chem. Soc. Chem. Commun. 1995, 777-778; H. Adams, F. J. Carver, C. A. Hunter, J. Chem. Soc. Chem. Commun. 1995, 809-810. A rotaxane was reported where one amide bond also seems to be inverted: D. A. Leigh, A. Murphy, J. P. Smart, A. M. Z. Slawin. Angew. Chem. 1997, 109, 752-756; Angew. Chem. Int. Ed. Engl. 1997, 36, 752-756.
    • (1995) J. Chem. Soc. Chem. Commun. , pp. 777-778
    • Ottens-Hildebrandt, S.1    Nieger, M.2    Rissanen, K.3    Rouvinen, J.4    Meier, S.5    Harder, G.6    Vögtle, F.7
  • 43
    • 14044255682 scopus 로고
    • S. Ottens-Hildebrandt, S. Meier, M. Nieger, F. Vögtle, E. Weber, Supramol. Chem. 1995, 5, 133-138; F. Vögtle, T. Dünnwald, T. Schmidt, Acc. Chem. Res. 1996, 29, 451-460; S. Braschohs, thesis, University of Bonn, 1998. In catenanes derived from these lactams. however, one amide group of each ring is inverted and the carbonyl points inwards to provide additional hydrogen bonds: S. Ottens- Hildebrandt, M. Nieger, K. Rissanen, J. Rouvinen, S. Meier, G. Harder, F. Vögtle, J. Chem. Soc. Chem. Commun. 1995, 777-778; H. Adams, F. J. Carver, C. A. Hunter, J. Chem. Soc. Chem. Commun. 1995, 809-810. A rotaxane was reported where one amide bond also seems to be inverted: D. A. Leigh, A. Murphy, J. P. Smart, A. M. Z. Slawin. Angew. Chem. 1997, 109, 752-756; Angew. Chem. Int. Ed. Engl. 1997, 36, 752-756.
    • (1995) J. Chem. Soc. Chem. Commun. , pp. 809-810
    • Adams, H.1    Carver, F.J.2    Hunter, C.A.3
  • 44
    • 0001282444 scopus 로고    scopus 로고
    • S. Ottens-Hildebrandt, S. Meier, M. Nieger, F. Vögtle, E. Weber, Supramol. Chem. 1995, 5, 133-138; F. Vögtle, T. Dünnwald, T. Schmidt, Acc. Chem. Res. 1996, 29, 451-460; S. Braschohs, thesis, University of Bonn, 1998. In catenanes derived from these lactams. however, one amide group of each ring is inverted and the carbonyl points inwards to provide additional hydrogen bonds: S. Ottens- Hildebrandt, M. Nieger, K. Rissanen, J. Rouvinen, S. Meier, G. Harder, F. Vögtle, J. Chem. Soc. Chem. Commun. 1995, 777-778; H. Adams, F. J. Carver, C. A. Hunter, J. Chem. Soc. Chem. Commun. 1995, 809-810. A rotaxane was reported where one amide bond also seems to be inverted: D. A. Leigh, A. Murphy, J. P. Smart, A. M. Z. Slawin. Angew. Chem. 1997, 109, 752-756; Angew. Chem. Int. Ed. Engl. 1997, 36, 752-756.
    • (1997) Angew. Chem. , vol.109 , pp. 752-756
    • Leigh, D.A.1    Murphy, A.2    Smart, J.P.3    Slawin, A.M.Z.4
  • 45
    • 0001282444 scopus 로고    scopus 로고
    • S. Ottens-Hildebrandt, S. Meier, M. Nieger, F. Vögtle, E. Weber, Supramol. Chem. 1995, 5, 133-138; F. Vögtle, T. Dünnwald, T. Schmidt, Acc. Chem. Res. 1996, 29, 451-460; S. Braschohs, thesis, University of Bonn, 1998. In catenanes derived from these lactams. however, one amide group of each ring is inverted and the carbonyl points inwards to provide additional hydrogen bonds: S. Ottens- Hildebrandt, M. Nieger, K. Rissanen, J. Rouvinen, S. Meier, G. Harder, F. Vögtle, J. Chem. Soc. Chem. Commun. 1995, 777-778; H. Adams, F. J. Carver, C. A. Hunter, J. Chem. Soc. Chem. Commun. 1995, 809-810. A rotaxane was reported where one amide bond also seems to be inverted: D. A. Leigh, A. Murphy, J. P. Smart, A. M. Z. Slawin. Angew. Chem. 1997, 109, 752-756; Angew. Chem. Int. Ed. Engl. 1997, 36, 752-756.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 752-756
  • 47
    • 0344212839 scopus 로고    scopus 로고
    • unpublished results
    • C. Seel, F. Vögtle, unpublished results. Quinone binding by a tetralactam of this type: C. A. Hunter, J. Chem. Soc. Chem. Commun. 1991, 749-751; C. A. Hunter, R. J. Shannon, J. Chem. Soc. Chem. Commun. 1996, 1361-1362.
    • Seel, C.1    Vögtle, F.2
  • 48
    • 37049088707 scopus 로고
    • C. Seel, F. Vögtle, unpublished results. Quinone binding by a tetralactam of this type: C. A. Hunter, J. Chem. Soc. Chem. Commun. 1991, 749-751; C. A. Hunter, R. J. Shannon, J. Chem. Soc. Chem. Commun. 1996, 1361-1362.
    • (1991) J. Chem. Soc. Chem. Commun. , pp. 749-751
    • Hunter, C.A.1
  • 49
    • 0002824281 scopus 로고    scopus 로고
    • C. Seel, F. Vögtle, unpublished results. Quinone binding by a tetralactam of this type: C. A. Hunter, J. Chem. Soc. Chem. Commun. 1991, 749-751; C. A. Hunter, R. J. Shannon, J. Chem. Soc. Chem. Commun. 1996, 1361-1362.
    • (1996) J. Chem. Soc. Chem. Commun. , pp. 1361-1362
    • Hunter, C.A.1    Shannon, R.J.2
  • 50
    • 37049083591 scopus 로고
    • Rotaxanes are molecular compounds that consist of one or more wheels and penetrating axles that are mechanically bound together and sterically prevented from dethreading by bulky stopper groups at both ends of the axles. Semirotaxanes and pseudorotaxanes are analogous "conventional" inclusion complexes that are not restrained mechanically from dissociation since the axles (here semi- and pseudoaxles, respectively) carry only one stopper or no stopper at all, respectively. We propose semi- and pseudorotaxanes that act as precursors in rotaxane syntheses to be called prerotaxanes. Compare with P. R. Ashton, D. Philp, N. Spencer, J. F. Stoddart, J. Chem. Soc. Chem. Commun. 1991, 1677-1679.
    • (1991) J. Chem. Soc. Chem. Commun. , pp. 1677-1679
    • Ashton, P.R.1    Philp, D.2    Spencer, N.3    Stoddart, J.F.4
  • 51
    • 0345506658 scopus 로고    scopus 로고
    • note
    • - and Br ions in the presence of tetrabutylammonium ions from an aqueous into an organic phase and maintain a clean 1:1 stoichiometry. The phase transfer of oxoanions is currently under investigation: H. Stephan. Forschungszentrum Rossendorf, personal communication.
  • 53
    • 0002287255 scopus 로고
    • (Eds.: H.-J. Schneider, H. Dürr), VCH, Weinheim, and references therein
    • a, the average of which is given for each anion. See C. S. Wilcox in Frontiers in Supramolecular Organic Chemistry and Photochemistry (Eds.: H.-J. Schneider, H. Dürr), VCH, Weinheim, 1991, pp. 123-143. and references therein.
    • (1991) Frontiers in Supramolecular Organic Chemistry and Photochemistry , pp. 123-143
    • Wilcox, C.S.1
  • 54
    • 0345506656 scopus 로고    scopus 로고
    • note
    • 1. that is, similar to the inorganic anions. Thiophenol, toluene-4-sulfonamide, and N-(4-tert-butylphenyl)-4-tert-butylphenylsulfonamide behave in a similar way.
  • 56
    • 0344212837 scopus 로고    scopus 로고
    • note
    • 2, hence we assume that the semirotaxanes formed with monoether 4 are not stable and thus do not act as prerotaxanes.
  • 57
    • 0344644426 scopus 로고    scopus 로고
    • note
    • 3 as the hase.
  • 58
    • 0344644425 scopus 로고    scopus 로고
    • note
    • 2 0.53 (0.48), p-xylylene 0.72 (the signal at lower field is overlapped in the free axle here) (0.79 and 0.80), oxophenyl H-2/60.37 (0.33): wheel: isophthaloyl H-2 0.46 and 0.48 (0.34 and 0.41).
  • 59
    • 0000124037 scopus 로고    scopus 로고
    • Deslipping had earlier been observed with similar rotaxanes: M. Händel, M. Plevoets, S. Gestermann, F. Vögtle, Angew. Chem. 1997, 109, 1248-1250; Angew. Chem. Int. Ed. Engl. 1996, 36, 1199-1201. Newer results reveal the process being of first order: F. Vögtle, A. Affeld, C. Heim, unpublished results.
    • (1997) Angew. Chem. , vol.109 , pp. 1248-1250
    • Händel, M.1    Plevoets, M.2    Gestermann, S.3    Vögtle, F.4
  • 60
    • 0345506654 scopus 로고    scopus 로고
    • Deslipping had earlier been observed with similar rotaxanes: M. Händel, M. Plevoets, S. Gestermann, F. Vögtle, Angew. Chem. 1997, 109, 1248-1250; Angew. Chem. Int. Ed. Engl. 1996, 36, 1199-1201. Newer results reveal the process being of first order: F. Vögtle, A. Affeld, C. Heim, unpublished results.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1199-1201
  • 61
    • 24244435868 scopus 로고    scopus 로고
    • unpublished results
    • Deslipping had earlier been observed with similar rotaxanes: M. Händel, M. Plevoets, S. Gestermann, F. Vögtle, Angew. Chem. 1997, 109, 1248-1250; Angew. Chem. Int. Ed. Engl. 1996, 36, 1199-1201. Newer results reveal the process being of first order: F. Vögtle, A. Affeld, C. Heim, unpublished results.
    • Vögtle, F.1    Affeld, A.2    Heim, C.3
  • 62
    • 0345506652 scopus 로고    scopus 로고
    • note
    • The new method has already been applied successfully to the synthesis of analogous rotaxanes with ester, thioester, sulfide, and acetal axles since the submission of this communication.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.