4.5 Article

Synthesis of Azepine- and Azocine-Annulated Heterocycles by Aromatic Aza-Claisen Rearrangement and Ring-Closing Metathesis

Journal

SYNTHESIS-STUTTGART
Volume -, Issue 5, Pages 863-869

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0029-1218620

Keywords

azepine; azocine; aza-Claisen rearrangement; ring-closing metathesis

Funding

  1. CSIR (New Delhi)

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Syntheses of hitherto unreported azepine- and azocine-annulated heterocycles have been developed in excellent yields via a catalyzed aromatic aza-Claisen rearrangement followed by ring-closing metathesis using Grubbs first-generation catalyst.

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