Advertisement

Aldol reactions have been reviewed several times as a specific topic in an exhaustive manner under different aspects.1,2,3,4,5,6,7,8,9

Due to the stormy development in this field of organic chemistry, especially in the last 10 years, there is a need for giving an update and summarizing the existing differing aldol methodologies. This is of particular importance in the field of organocatalysed aldol addition.

Keywords

Aldol Reaction Transition State Model Stereochemical Outcome Exhaustive Manner Open Transition State 
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.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Paterson I, Franklin AS (1994) Contemp Org Synth 1:317CrossRefGoogle Scholar
  2. 2.
    Braun M (1996) In: Houben-Weyl, Methoden der Organischen Chemie, Helmchen G, Hoffmann RW, Mulzer J, Schaumann E (eds). Thieme, Stuttgart. vol E21b, p 1603Google Scholar
  3. 3.
    Machajewski TD, Wong CH (2000) Angew Chem In Ed 39:1352CrossRefGoogle Scholar
  4. 4.
    Palomo C, Oiarbide M, Garcia JM (2002) Chem Eur J 8:36CrossRefGoogle Scholar
  5. 5.
    Palomo C, Oiarbide M, Garcia JM (2004) Chem Soc Rev 33:65CrossRefGoogle Scholar
  6. 6.
    Mahrwald R (ed) (2004) Modern Aldol Reactions. Wiley-VCH, WeinheimGoogle Scholar
  7. 7.
    Schetter B, Mahrwald R (2006) Angew Chem Int Ed 45:7506CrossRefGoogle Scholar
  8. 8.
    Schetter B, Mahrwald R (2008) In: Science of Synthesis, Clayden J (ed). Thieme, Stuttgart, p 847Google Scholar
  9. 9.
    Geary LM, Hultin PG (2009) Tetrahedron: Asymm 20:131CrossRefGoogle Scholar
  10. 10.
    Ivanoff D, Spassoff A (1931) Bull Soc Chim Fr 49:371Google Scholar
  11. 11.
    Braun M (2004) In: Modern Aldol Reactions, Mahrwald R (ed). Wiley-VCH, Weinheim, vol 1, p 1CrossRefGoogle Scholar
  12. 12.
    van Draanen NA, Arseniyadis S, Crimmins MT, Heathcock CH (1991) J Org Chem 56:2499CrossRefGoogle Scholar
  13. 13.
    Evans DA, Clark JS, Metternich R, Novack VJ, Sheppard GS (1990) J Am Chem Soc 112:866CrossRefGoogle Scholar
  14. 14.
    Evans DA, Burch JD, Hu E, Jaeschke G (2008) Tetrahedron 64:4671CrossRefGoogle Scholar
  15. 15.
    Menche D, Arikan, F, Li J (2008) Org Lett 10:3521CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V 2009

Personalised recommendations