Skip to main content

Part of the book series: Teubner Studienbücher Chemie ((TSBC))

  • 1138 Accesses

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 54.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literatur

  1. E. Erlenmeyer, Justus Liebigs Ann. Chem. 1892, 277, 137–163.

    Google Scholar 

  2. M. S. Newman, B. J. Magerlein, Org. React. 1949, 5, 413–440.

    CAS  Google Scholar 

  3. G. Berti, Top. Stereochem. 1973, 7, 210–218.

    Google Scholar 

  4. J. A. Deyrup, J. Org. Chem. 1969, 34, 2724–2727.

    Article  CAS  Google Scholar 

  5. M. Delépine, Bull. Soc. Chim. Fr. 1895, 13, 352–361.

    Google Scholar 

  6. N. Blazevic, D. Kolbah, B. Belin, V. Sunjic, F. Kafjez, Synthesis 1979, 161–176.

    Google Scholar 

  7. B. C. Challis, A. R. Butler in The Chemistry of the Amino Group (Hrsg.: S. Patai), Wiley, New York, 1968, S. 305–320.

    Google Scholar 

  8. K. Schank in The Chemistry of the Diazonium and Diazo Groups (Hrsg.: S. Patai), Wiley, New York, 1978, Bd. 2, S. 645–657.

    Book  Google Scholar 

  9. J. H. Ridd, Q. Rev. Chem. Soc. 1961, 75, 418–441.

    Article  Google Scholar 

  10. S. H. Korzeniowski, A. Leopold, J. R. Beadle, M. F. Ahern, W. A. Sheppard, R. K. Khanna, G. W. Gokel, J, Org. Chem. 1981, 46, 2153–2159.

    Article  CAS  Google Scholar 

  11. R. A. Bartsch in The Chemistry of Functional Groups, Supp. C (Hrsg.: S. Patai, Z. Rappoport), Wiley, New York, 1983, Bd. 1, S. 889–915.

    Google Scholar 

  12. N. Kornblum, D. C. Iffland, J. Am. Chem. Soc, 1949, 71, 2137–2143.

    Article  CAS  Google Scholar 

  13. M. Regitz in The Chemistry of the Diazonium and Diazo Groups (Hrsg.: S. Patai), Wiley, New York, 1978, Bd. 2, S. 659–708.

    Book  Google Scholar 

  14. O. Diels, K. Alder, Justus Liebigs Ann. Chem. 1928, 460, 98–122.

    Article  CAS  Google Scholar 

  15. J. A. Norton, Chem. Rev. 1942, 31, 319–523.

    Article  CAS  Google Scholar 

  16. J. G. Martin, R. K. Hill, Chem. Rev. 1961, 61, 537–562.

    Article  CAS  Google Scholar 

  17. W. Carruthers, Cycloaddition Reactions in Organic Synthesis, Pergamon Press, Oxford, 1990, S. 1–208.

    Google Scholar 

  18. S. M. Weinreb, P. M. Scola, Chem. Rev. 1989, 89, 1525–1534.

    Article  CAS  Google Scholar 

  19. B. Rickborn, Org. React. 1998, 52, 1–393.

    CAS  Google Scholar 

  20. B. Rickborn, Org. React. 1998, 53, 223–629.

    CAS  Google Scholar 

  21. D. Craig, Chem. Soc. Rev. 1987, 16, 187–238.

    Article  CAS  Google Scholar 

  22. J. Sauer, R. Sustmann, Angew. Chem. 1980, 92, 773–801

    Article  CAS  Google Scholar 

  23. J. Sauer, R. Sustmann, Angew. Chem. Int. Ed. Engl. 1980, 19, 779.

    Article  Google Scholar 

  24. W. Oppolzer, Angew. Chem. 1984, 96, 840–854

    Article  CAS  Google Scholar 

  25. W. Oppolzer, Angew. Chem. Int. Ed. Engl 1984, 23, 876.

    Article  Google Scholar 

  26. J. Sauer, Angew. Chem. 1967, 79, 76–94

    Article  Google Scholar 

  27. J. Sauer, Angew. Chem. Int. Ed. Engl. 1967, 6, 16.

    Article  CAS  Google Scholar 

  28. R. B. Woodward, R. Hoffmann, Die Erhaltung der Orbitalsymmetrie, VCH, Weinheim, 1970.

    Google Scholar 

  29. I. Fleming, Grenzorbitale und Reaktionen organischer Verbindungen, VCH, Weinheim, 1979, S. 123–172.

    Google Scholar 

  30. P. G. Gassman, D. B. Gorman, J. Am. Chem. Soc. 1990, 112, 8624–8626.

    Article  CAS  Google Scholar 

  31. A. J. Fatiadi, Synthesis 1987, 749–789.

    Google Scholar 

  32. J. Sauer, H. Wiest, Angew. Chem. 1962, 74, 353

    Article  CAS  Google Scholar 

  33. J. Sauer, H. Wiest, Angew. Chem. Int. Ed. Engl. 1962, 1, 268.

    Article  Google Scholar 

  34. C. Cativiela, J. I. Garcia, J. A. Mayoral, L. Salvatella, Chem. Soc. Rev. 1996, 25, 209–218.

    Article  Google Scholar 

  35. K. Matsumoto, A. Sera, Synthesis 1985, 999–1027.

    Google Scholar 

  36. L. F. Tietze, T. Hübsch, J. Oelze, C. Ott, W. Tost, G. Wörner, M. Buback, Chem. Ber. 1992, 125, 2249–2258.

    Article  CAS  Google Scholar 

  37. H. Waldmann, Angew. Chem. 1991, 103, 1335–1337

    Article  CAS  Google Scholar 

  38. H. Waldmann, Angew. Chem. Int. Ed. Engl. 1991, 30, 1306.

    Article  Google Scholar 

  39. H. B. Kagan, O. Riant, Chem. Rev. 1992, 92, 1007–1019.

    Article  CAS  Google Scholar 

  40. H. Hopf, G. Weber, K. Menke, Chem. Ber. 1980, 113, 531–541.

    Article  Google Scholar 

  41. E. Ciganek, Org React. 1984, 32, 1–374.

    CAS  Google Scholar 

  42. W.-D. Fessner, C. Grund, H. Prinzbach, Tetrahedron Lett. 1989, 30, 3133–3136.

    Article  CAS  Google Scholar 

  43. L. F. Tietze, U. Beifuss, Angew. Chem. 1993, 105, 137–170

    Article  CAS  Google Scholar 

  44. L. F. Tietze, U. Beifuss, Angew. Chem. Int. Ed. Engl. 1993, 52, 131.

    Article  Google Scholar 

  45. J. A. Winkler, Chem. Rev. 1996, 96, 167–176.

    Article  CAS  Google Scholar 

  46. H. Waldmann, Synthesis 1996, 535–551.

    Google Scholar 

  47. H. E. Zimmerman, G. L. Grunewald, J. Am. Chem. Soc. 1966, 88, 183–184.

    Article  CAS  Google Scholar 

  48. H. E. Zimmerman, D. Armesto, Chem. Rev. 1996, 96, 3065–3112.

    Article  CAS  Google Scholar 

  49. D. Döpp, H. E. Zimmerman, Methoden Org. Chem. (Houben-Weyl) 1975, Bd.4/5a, S. 413–432.

    Google Scholar 

  50. L. A. Paquette, E. Bay, A. Yeh Ku, N. G. Rondan, K. N. Houk, J. Org. Chem. 1982, 47, 422–428.

    Article  CAS  Google Scholar 

  51. H. E. Zimmerman, Angew. Chem. 1969, 81, 45–55

    Article  Google Scholar 

  52. H. E. Zimmerman, Angew. Chem. Int. Ed. Engl. 1969, 8, 1.

    Article  CAS  Google Scholar 

  53. M. Demuth, G. Mikhail, Synthesis 1989, 145–162.

    Google Scholar 

  54. K. H. Dötz, Angew. Chem. 1975, 87, 672–673

    Article  Google Scholar 

  55. K. H. Dötz, Angew. Chem. Int. Ed. Engl. 1975, 14, 644.

    Article  Google Scholar 

  56. N. E. Schore, Chem. Rev. 1988, 88, 1081–1119.

    Article  CAS  Google Scholar 

  57. J. Mulzer, H.-U. Reissig, H.-J. Altenbach, M. Braun, K. Krohn, Organic Synthesis Highlights, VCH, Weinheim, 1991, S. 186–191.

    Google Scholar 

  58. K. S. Chan, G. A. Peterson, T. A. Brandvold, K. L. Faron, C. A. Challener, C. Hyldahl, W. D. Wulff, J. Organomet. Chem. 1987, 334, 9–56.

    Article  CAS  Google Scholar 

  59. J. S. McCallum, F.-A. Kunng, S. R. Gilbertson, W. D. Wulff, Organome-tallics 1988, 7, 2346–2360.

    Article  CAS  Google Scholar 

  60. M. F. Semmelhack, J. J. Bozell, L. Keller, T. Sato, E. J. Spiess, W. D. Wulff, A. Zask, Tetrahedron 1985, 41, 5803–5812.

    Article  CAS  Google Scholar 

  61. K. H. Dötz, Angew. Chem. 1984, 96, 573–594

    Article  Google Scholar 

  62. K. H. Dötz, Angew. Chem. Int. Ed. Engl. 1984, 23, 587.

    Article  Google Scholar 

  63. L. Roth, Krebserzeugende Stoffe, Wissenschaftliche Verlagsgesellschaft, Stuttgart, 1983, S. 16.

    Google Scholar 

  64. K. H. Dötz, M. Popall, Chem. Ber. 1988, 121, 665–672.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 2004 B. G. Teubner Verlag / GWV Fachverlage GmbH, Wiesbaden

About this chapter

Cite this chapter

Laue, T., Plagens, A. (2004). D. In: Namen- und Schlagwort-Reaktionen der Organischen Chemie. Teubner Studienbücher Chemie. Vieweg+Teubner Verlag. https://doi.org/10.1007/978-3-322-96805-0_5

Download citation

  • DOI: https://doi.org/10.1007/978-3-322-96805-0_5

  • Publisher Name: Vieweg+Teubner Verlag

  • Print ISBN: 978-3-519-33526-9

  • Online ISBN: 978-3-322-96805-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics