4.7 Article

Cyanative alkene-aldehyde coupling: Ni(0)-NHC-Et2AlCN mediated chromanol synthesis with high cis-selectivity at room temperature

Journal

CHEMICAL COMMUNICATIONS
Volume 46, Issue 3, Pages 466-468

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b918626c

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Funding

  1. Center of Novel Functional Molecule
  2. The Chinese University of Hong Kong
  3. Incentive Research Scheme [4440138]
  4. Hong Kong General Research Fund [2160344]

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Described are several classes of Ni(0) mediated cyanative alkene-aldehyde coupling reactions, providing 6-membered cores, which complement existing cyclization technology in several respects. Et2AlCN was used as both a cyclization accelerator and CN source. The NHC ligand may have a positive effect in differentiating reductive elimination and syn-beta-hydride elimination.

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