4.8 Article

Asymmetric Construction of Quaternary Carbon Centers by Sequential Conjugate Addition of Lithium Amide and in Situ Alkylation: Utility in the Synthesis of (-)-Aspidospermidine

Journal

ORGANIC LETTERS
Volume 11, Issue 3, Pages 653-655

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol802759j

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Funding

  1. Grant-in-Aid for Young Scientists (B)
  2. Grant-in-Aid for Scientific Research (A)
  3. Targeted Proteins Research Program of the Ministry of Education. Culture, Sports, Science, and Technology, Japan
  4. JSPS fellowship
  5. Grants-in-Aid for Scientific Research [20249002] Funding Source: KAKEN

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Chiral diether ligand-controlled asymmetric conjugate addition of a lithium amide to cyclopentenecarboxylate and subsequent in situ alkylation gave a chiral cyclopentane derivative bearing a quaternary carbon with high enantio- and diastereoselectivity. The cyclopentane derivative was converted successfully to (-)-aspidospermidine.

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