4.6 Article

A facile method for the synthesis of oxindole based quaternary alpha-aminonitriles via the Strecker reaction

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 8, Issue 17, Pages 3847-3850

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0ob00174k

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Funding

  1. Natural Science Foundation of China [20902025]
  2. East China Normal University

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The direct alpha-cyanoamination of isatins using TMSCN has been developed, which is carried out in methanol without any catalyst. A new bifunctional cinchona alkaloid-based phosphinamide catalyst 7 could promote the Strecker reaction of isatins derived ketimine with TMSCN in up to 74% ee.

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