4.8 Article

Isoleucine-Catalyzed Direct Asymmetric Aldol Addition of Enolizable Aldehydes

Journal

ORGANIC LETTERS
Volume 14, Issue 8, Pages 2180-2183

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol300754n

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Funding

  1. Deutsche Forschungsgemeinschaft
  2. Bayer Pharma AG
  3. Chemtura Organometallics GmbH Bergkamen
  4. Bayer Services GmbH
  5. BASF AG
  6. Sasol GmbH

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Isoleucine-catalyzed direct enantioselective aldol additions between enolizable aldehydes are reported. Intermediate acetal structures dictate the configurative outcome and were supported by a hydrogen bond. This direct isoleucine-catalyzed aldol addition represents a welcome complement to both proline- and histidine-catalyzed aldol additions of enolizable aldehydes.

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