4.7 Article

Aza-oxindole synthesis via base promoted Truce-Smiles rearrangement

Journal

CHEMICAL COMMUNICATIONS
Volume 48, Issue 89, Pages 10957-10959

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cc36068c

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Funding

  1. Swiss National Science Foundation
  2. University of Geneva

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A novel efficient NaOtBu-mediated protocol for the synthesis of 3,3-disubstituted aza-oxindoles proceeds via a Truce-Smiles rearrangement-cyclisation pathway.

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