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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2Topics & keywords
Topics
Keywords
- Aldol reaction
- Enantioselective synthesis
- Chemistry
- Yield (engineering)
- Polyketide
- Catalysis
- Stereochemistry
- Organic chemistry
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