4.8 Article

Enantioselective [2+2+2] Cycloaddition Reaction of Isocyanates and Allenes Catalyzed by Nickel

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 132, Issue 45, Pages 15836-15838

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja105541r

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Funding

  1. MEXT [22106520]
  2. Grants-in-Aid for Scientific Research [22106520] Funding Source: KAKEN

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The enantioselective intermolecular [2 + 2 + 2] cycloaddition reaction of two molecules of isocyanate and one molecule of allene is catalyzed by a nickel(0)/(S,S)-i-Pr-FOXAP complex, providing an efficient access to enantiomerically enriched dihydropyrimidine-2,4-diones.

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