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Analytical and Bioanalytical Chemistry

, Volume 399, Issue 5, pp 1811–1814 | Cite as

The 2010 Chemistry Nobel Prize to R.F. Heck, E. Negishi, and A. Suzuki for palladium-catalyzed cross-coupling reactions

  • Didier AstrucEmail author
Feature Article

Keywords

Nobel Prize Heck Reaction Reductive Elimination Suzuki Reaction Organic Halide 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. 1.
    Heck RF (1982) Org React 27:345–390Google Scholar
  2. 2.
    Negishi E, Huang Z, Huang G, Mohan S, Wang C, Hattori H (2008) Acc Chem Res 41:1474–1485CrossRefGoogle Scholar
  3. 3.
    Suzuki A (2002) In: Astruc D (ed) Modern arene chemistry. Wiley-VCH, Weinheim, pp 53–106CrossRefGoogle Scholar
  4. 4.
    de Meyere A, Diederich F (eds) (2004) Metal-catalyzed cross coupling reactions. Wiley-VCH, WeinheimGoogle Scholar
  5. 5.
    Astruc D (2007) Organometallic chemistry and catalysis. Springer, HeidelbergGoogle Scholar
  6. 6.
    Karash MS, Fields EK (1941) J Am Chem Soc 63:2316CrossRefGoogle Scholar
  7. 7.
    Smidt J, Hafner W, Jira R, Sedlmeier J, Sieber R, Rüttinger, Kojer RH (1959) Angew Chem 71:176CrossRefGoogle Scholar
  8. 8.
    Heck RF (1968) J Am Chem Soc 90:5518–5526CrossRefGoogle Scholar
  9. 9.
    Heck RF (1968) J Am Chem Soc 90:5526–5531CrossRefGoogle Scholar
  10. 10.
    Heck RF (1968) J Am Chem Soc 90:5531–5534CrossRefGoogle Scholar
  11. 11.
    Heck RF (1968) J Am Chem Soc 90:5538–5542CrossRefGoogle Scholar
  12. 12.
    Heck RF (1968) J Am Chem Soc 90:5542–5546CrossRefGoogle Scholar
  13. 13.
    Vaska L (1968) Acc Chem Res 1:335–343CrossRefGoogle Scholar
  14. 14.
    Knochel P (1993) Chem Rev 93:2117–2188CrossRefGoogle Scholar
  15. 15.
    Knochel P, Almena Perea JJ, Jones P (1998) Tetrahedron 54:8275–8319CrossRefGoogle Scholar
  16. 16.
    Miyaura N, Suzuki A (1979) Chem Commun 866–867Google Scholar
  17. 17.
    Miyaura N, Yamada K, Suzuki A (1979) Tetrahedron Lett 20:3437–3440CrossRefGoogle Scholar
  18. 18.
    Miyaura N, Suzuki A (1995) Chem Rev 95:2457–2483CrossRefGoogle Scholar
  19. 19.
    Sonogashira K, Tohda Y, Hagihara N (1975) Tetrahedron Lett 16:4467–4470CrossRefGoogle Scholar
  20. 20.
    Fu GC (2008) Acc Chem Res 41:1555–1564CrossRefGoogle Scholar
  21. 21.
    Martin R, Buchwald SL (2008) Acc Chem Res 41:1461–1473CrossRefGoogle Scholar
  22. 22.
    Herrmann WA (2002) Angew Chem Int Ed 41:1290–1309CrossRefGoogle Scholar
  23. 23.
    Marion N, Nolan SP (2008) Acc Chem Res 41:1440–1449CrossRefGoogle Scholar
  24. 24.
    Diallo AK, Ornelas C, Salmon L, Ruiz J, Astruc D (2007) Angew Chem Int Ed 46:8644–8648CrossRefGoogle Scholar
  25. 25.
    Danishefsky SJ, Masters JJ, Young WB, Link JT, Snyder LB, Magee TV, Jung DK, Isaac RCA, Bornmann WG, Alaimo CA, Coburn CA, Di Grandi MJ (1999) J Am Chem Soc 118:2843–2859CrossRefGoogle Scholar
  26. 26.
    Schrock AK (1989) US Patent 4812:588Google Scholar
  27. 27.
    Tamura M, Kochi JK (1971) J Am Chem Soc 44:1483–1484Google Scholar
  28. 28.
    Tamura M, Kochi JK (1971) J Am Chem Soc 44:1485–1486Google Scholar
  29. 29.
    Tamura M, Kochi JK (1971) J Am Chem Soc 44:1487–1488CrossRefGoogle Scholar
  30. 30.
    Corriu RJP, Masse JP (1972) Chem Commun 44–45Google Scholar
  31. 31.
    Tamao K, Sumitani K, Kumada M (1972) J Am Chem Soc 94:4374–4375CrossRefGoogle Scholar
  32. 32.
    Fauvarque J-F, Jutand A (1977) J Organomet Chem 132:C17–C19CrossRefGoogle Scholar
  33. 33.
    Amatore C, Jutand A (2000) Acc Chem Res 33:314–321CrossRefGoogle Scholar
  34. 34.
    Nobelprize.org (2010) The Nobel Prize in chemistry 2010. http://nobelprize.org/nobel_prizes/chemistry/laureates/2010/

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  1. 1.Institut des Sciences MoléculairesTalence CedexFrance

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