articleJournal of the American Chemical SocietyMay 8, 2002Closed access

The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes

California Institute of Technology

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Abstract

The first enantioselective catalytic direct cross-aldol reaction that employs nonequivalent aldehydes has been accomplished using proline as the reaction catalyst. Structural variation in both the aldol donor (R1 = Me, n-Bu, Bn, 91 to >99%) and aldol acceptor (R2 = I-Pr, I-Bu, c-C6H11, Et, Ph, 97-99% ee) are possible while maintaining high reaction efficiency (75-88% yield). Significantly, this new aldol variant allows facile enantioselective access to a broad range of beta-hydroxy aldehydes which are valuable intermediates in polyketide syntheses.

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Authors

2

Topics & keywords

Keywords
  • Aldol reaction
  • Enantioselective synthesis
  • Chemistry
  • Yield (engineering)
  • Polyketide
  • Catalysis
  • Stereochemistry
  • Organic chemistry
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